Patent Application
20190388362
The present invention relates to a method of predicting or diagnosing oral precancer or oral cancer, and more particularly, to a method of providing information for the prediction or diagnosis of oral precancer or oral cancer comprising Axin2 gene expression or snail (SNAI1) gene expression in a tissue sample of an oral leukoplakia or an oral submucous fibrosis, and a use of a compound for inhibiting Axin2 gene expression or Snail gene expression for delaying the progression of or inhibiting oral precancerous lesions and recurrent oral cancer.
It is well known that oral leukoplakia with a white lesion in the oral cavity contains submucosal fibrosis and may develop malignancy (van der Waal I., Med Oral Patol Oral Cir Bucal., 19:e386, 2014; Holmstrup P et al., Oral Oncol, 42:461, 2006; Holmstrup P., Oral Oncol 45:549, 2009). Oral leukoplakia occurs in about 1% of all age groups, and the malignancy rate of untreated lesions has been reported to be 2% to 3% per year (van der Waal I., Med Oral Patol Oral Cir Bucal., 19:e386, 2014). Meanwhile, the risk of recurrence after surgical treatment of non-homologous leukoplakia has been estimated up to 20%, and squamous cell carcinoma developed from leukoplakia has a low survival rate (Holmstrup P et al., Oral Oncol, 42:461, 2006). For the diagnosis of oral leukoplakia, many studies have been conducted to find predictive markers of malignancy including general pathologic examination, clinical parameters, and biomarkers, but the prediction rate is still limited.
Known risk factors for oral leukoplakia malignancy are age, female, long duration of leukoplakia, large size, medical history of head and neck cancer, non-homologous clinical appearance, the presence of histologic features of dysplasia, and leukoplakia lesions at the tongue edge or mouth bottom. In addition, predictive factors for oral leukoplakia malignancy are the presence of Candida albicans, the possibility of staining of leukoplakia lesions with toluidine blue, abnormal expression of numerous molecular markers including p16INK4a and Ki-67, chromosomal instability, and loss of heterozygosity in 9p and mutated TP53 (Abdulrahim M H et al., PLoS One, 8:e73738, 2013; Zhang L et al., Cancer Res, 65:8017, 2005; Nasser W et al., J Oral Pathol Med, 40:629, 2011; Siebers T J et al., Oral Oncology 49:1121, 2013; Graveland A P et al., Oral Oncol, 49:1129, 2013). However, it is still difficult to accurately estimate potential risk factors for the development of oral squamous cell carcinoma (OSCC) with high reproducibility and certainty.
Epithelial-to-mesenchymal transition (EMT) silences epithelial cell characteristics and transforms the cell state into an invasive phenotype to exhibit mesenchymal characteristics (Dang T T et al., Cancer Res, 75:3925, 2015), and Snail1, which is a zinc-finger transcriptional inhibitor, plays an important role in EMT involving complementary morphogenesis in cancer. The snail1 protein is stabilized by the activation of the Wnt signal through the inhibition of serial phosphorylation of GSK-3. The Axin2 scaffolding protein, which is a typical transcription target for the TCF/LEF complex, regulates the nucleus cytoplasmic shuttle of GSK-3 to stabilize the nuclear Snail. Simultaneous expression of Axin2 and Snail1 in acute breast cancer and colorectal cancer is well known, but clinical significance and expression of the Wnt gene is not well known.
Although early EMT studies have focused primarily on metastatic processes, studies are now being conducted on the initial activation of EMT-related genes in preneoplastic lesions and non-invasive tumors. For example, a major pathogen of Helicobactor pylori in the human stomach strongly induces Snail-mediated EMT in gastric epithelial cells, and Snail1 is increased in non-invasive endometrial carcinoma. In addition, in EMT of oral leukoplakia, E-cadherin is decreased in moderate dysplasia during malignant processes, which may be determined as a high risk of malignancy (von Zeidler S V et al., BMC Cancer, 14:972, 2014). These results suggest that EMT gene expression in oral precancer has the potential to play a role in cancer progression.
In addition, unlike other cancers, in the case of oral cancer, there are many cases in which it is very difficult to perform surgical removal due to the presence of multiple precancerous lesions such as leukoplakia or erythroplakia by the field cancerization theory, and even after progressing to oral cancer, precancerous lesions and advanced cancer continue to recur (Slaughter D P et al, Cancer 1953, 6, 963-968; Mohan M & Jagannathan N, Oncology Rev 2014, 8:244, 13-19). In this case, proper therapeutic materials for precancerous lesions and advanced cancer have not yet been known, and most cases rely on surgical resection, but repeated surgical operations still have many limitations.
Therefore, as a result of having made intensive efforts to develop a method of diagnosing and treating the malignant development of oral leukoplakia, the inventors of the present invention confirmed that the progression and risk of oral epithelial cancer could be diagnosed, and when treated with a substance for inhibiting Axin2 and Snail, oral leukoplakia treatment was possible, thus completing the present invention.
Therefore, the present invention has been made in view of the above problems, and it is an object of the present invention to provide a method of providing information for the prediction or diagnosis of oral precancer or oral cancer.
It is another object of the present invention to provide a kit for predicting or diagnosing oral precancer or oral cancer.
It is a further object of the present invention to provide a pharmaceutical composition for inhibiting the progression of oral precancer or oral cancer.
In accordance with an aspect of the present invention, the above and other objects can be accomplished by the provision of a method of providing information for the prediction or diagnosis of oral precancer or oral cancer, the method comprising confirming an expression of the Axin2 gene or the Snail gene in a tissue sample of an oral leukoplakia or an oral submucous fibrosis.
In accordance with another aspect of the present invention, there is provided a composition for predicting or diagnosing oral precancer or oral cancer, the composition comprising an agent for confirming expression of the Axin2 gene or the Snail gene.
In accordance with another aspect of the present invention, there is provided a kit for predicting or diagnosing oral precancer or oral cancer, the kit comprising an agent for confirming expression of the Axin2 gene or the Snail gene.
In accordance with another aspect of the present invention, there is provided a pharmaceutical composition for delaying or inhibiting progression of an oral precancerous lesion and recurrent oral cancer, the pharmaceutical composition comprising, as an active ingredient, a compound for inhibiting expression of the Axin2 gene or the Snail gene.
In accordance with another aspect of the present invention, there is provided a method of delaying or inhibiting progression of an oral precancerous lesion and recurrent oral cancer, the method comprising administering a composition for inhibiting expression of the Axin2 gene or the Snail gene.
In accordance with another aspect of the present invention, there is provided a use of a compound for inhibiting expression of the Axin2 gene or the Snail gene for delaying or inhibiting progression of an oral precancerous lesion and recurrent oral cancer.
In accordance with another aspect of the present invention, there is provided a use of a compound for inhibiting expression of the Axin2 gene or the Snail gene for preparing a drug for delaying or inhibiting progression of an oral precancerous lesion and recurrent oral cancer.
In accordance with another aspect of the present invention, there is provided a method of predicting or diagnosing oral precancer or oral cancer, the method including confirming an expression level of the Axin2 gene or the Snail gene.
In accordance with another aspect of the present invention, there is provided a method of treating oral precancer or recurrent oral cancer, the method including administering a therapeutically effective amount of a compound for inhibiting expression of the Axin2 gene or the Snail gene to an individual in need thereof.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
Unless defined otherwise, technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art to which the present invention pertains. Generally, the nomenclature used herein is well known in the art and commonly used.
In the present invention, it was confirmed that Axin2 and Snail expression patterns were changed in oral leukoplakia malignancy, and it was confirmed whether Axin2 and Snail could be used as biomarkers for predicting oral leukoplakia malignancy. For immunohistochemical staining of Axin2 and Snail, oral mucosa samples of oral leukoplakia and oral submucous fibrosis, which were histopathologically confirmed, were used, and histological patterns of Axin2 and Snail were analyzed and classified. The correlation between clinicopathologic factors and malignancy of oral leukoplakia was confirmed by creating a nomogram graphically represented for 17 years and 10 months.
In one embodiment, the present invention relates to a method of providing information for the prediction or diagnosis of oral precancer or oral cancer, the method being characterized by confirming an expression level of the Axin2 gene or the Snail gene.
In the present invention, the confirmation of the expression level of the Axin2 gene or the Snail gene may be performed using an oral leukoplakia tissue sample or an oral submucous fibrosis tissue sample.
In the present invention, the confirmation of the expression level of the Axin2 gene or the Snail gene may be performed by comparing an expression level of the Axin2 gene or the Snail gene in lesion tissues derived from patients with oral leukoplakia or oral submucous fibrosis with that in tissues of healthy individuals.
In the present invention, the confirmation of the expression level of the gene may be performed using a method selected from the group consisting of RT-PCR, immunohistochemical staining, and enzyme-linked immunosorbent assay (ELISA).
In the present invention, the expression of Axin2 and Snail was evaluated in a long-term follow-up group of oral precancerous lesions.
The term “oral precancer” as used herein refers to a disease which can develop into oral cancer, and includes oral leukoplakia, oral erythroplakia, oral submucous fibrosis, and the like. Oral precancer patients include patients that have received surgical operations for oral cancer and persistent precancerous lesions and advanced cancer recurrence over several years according to the field cancerization theory.
In the present invention, the oral cancer may be squamous cell carcinoma, malignant lymphoma, sarcoma, malignant melanoma, or the like, preferably squamous cell carcinoma.
In the present invention, EMT genes were studied as a predictive role of malignant progression of oral precancer. Although many genes contain Canonical Wnt signals, we have studied the GSK-3 scaffolding protein Axin2 and the E-cadherin transcription inhibitor Snail to assess the potential of this biomarker.
In the absence of the Wnt signal, GSK3 degrades β-catenin and plays an inhibiting role in maintaining an epithelial phenotype. Snail inhibits the transcription of the E-cadherin gene to express a mesenchymal phenotype. In addition, Snail activity is inhibited by selective phosphorylation of GSK3 (Carver E A et al., Mol Cell Biol, 21:8184, 2001; Zhou B P et al., Nat Cell Biol, 6:931-40, 2004; 21. Bachelder R E et al., J Cell Biol, 168:29, 2005; Yook J I et al., J Biol Chem, 280:11740, 2005).
In the present invention, the presence of Axin2 is closely associated with the malignant progression of oral precancerous lesions. Considering that Axin2 is a typical downstream factor in the canonical Wnt pathway, results indicate that increased Wnt activity may play an important role in the malignancy of oral leukoplakia.
In one embodiment of the present invention, it was confirmed that, while the normal mucosal epithelium exhibits the cytoplasmic expression of Axin2 and Snail, Axin2 and Snail were not expressed in the nucleus. It was also confirmed that, compared to a normal control, Snail of the epithelium was significantly expressed in both the nucleus and cytoplasm in oral leukoplakia lesions.
In another embodiment of the present invention, a biopsy sample of oral submucous fibrosis was further examined. Oral submucous fibrosis is a chronic progressive fibrous mucosal disease of the oral cavity and has a potential risk of malignancy. Immunohistochemical staining studies revealed similar expression patterns of Axin2 and Snail in epithelial lesions of oral submucous fibrosis.
However, Axin2 has been found to act as a tumor gene by promoting Snail-mediated EMT and metastatic activity during cancer progression (Klar M et al., Breast Cancer Res Treat, 112:523, 2008). In addition, reducing Axin2 expression decreases Snail activity and returns EMT, thereby inhibiting invasive and metastatic tumor activity (Klar M et al., Breast Cancer Res Treat, 112:523, 2008).
In the present invention, it was confirmed from clinicopathological data that there was no significant association between tissue Axin2 expression of oral leukoplakia and clinical variables, and when a Snail-positive oral leukoplakia patient group was reevaluated, excellent Axin2 expression was considerably associated with the risk of malignancy. Interestingly, patients with oral submucous fibrosis showed patterns similar to clinicopathological association with regard to the risk of malignancy. Furthermore, in our studies, univariate and multivariate analyses have shown that gender, age, Snail expression, and Axin2 expression are significantly associated with the risk of malignancy of oral leukoplakia patients. In particular, Axin2 overexpression was found to be the most important factor for predicting the risk of malignancy in Snail-positive oral leukoplakia patients. Therefore, it is concluded that Snail activity is caused by the loss of function of the scaffolding protein Axin2 and the inactivation of destructive complexes during malignant processes in patients with oral leukoplakia.
In the present invention, based on cross-sectional and retrospective cohort study results, a nomogram was created to evaluate the risk factors of malignancy of oral leukoplakia. Nomograms of
The present invention provides predictive values of Axin2 and Snail expression which are predictive of oral leukoplakia developing into oral squamous epithelial cell carcinoma. Since there is no effective treatment for malignancy, biomarker investigation for risk prediction is a method to improve cancer-free survival time in patients with oral leukoplakia. In addition, to predict malignancy in other oral mucosal lesions having a potential risk of malignancy such as oral submucous fibrosis, it is useful to evaluate expression patterns of Axin2 and Snail in tissues.
In another embodiment, the present invention relates to a composition or kit for predicting or diagnosing oral precancer or oral cancer, which includes an agent for confirming the expression of the Axin2 gene or the Snail gene.
In the present invention, the agent for confirming the expression of the gene may be selected from the group consisting of an antibody or aptamer that specifically binds to the Axin2 protein or the Snail protein, a primer that specifically amplifies the Axin2 gene or the Snail gene, and a probe specifically binding to the Axin2 gene or the Snail gene.
In the method of the present invention, to provide information that is useful for the prediction or diagnosis of oral precancer or oral cancer, a method of measuring an expression level of the gene may be performed by, preferably, genetic analysis.
When the present invention is practiced based on genetic analysis, primers or probes that specifically bind to the listed target gene sequences are used. In the present invention, when primers are used, gene amplification is performed to examine an expression level of the target gene. Since the present invention analyzes the expression level of a gene, the expression level of the gene is determined by examining an mRNA expression level of a target gene in a sample (e.g., a cell sample or tissue sample) to be analyzed. Thus, in the present invention, the gene amplification reaction may be, in principle, performed using mRNA in a sample as a template and a primer that binds to mRNA or cDNA. To obtain mRNA, total RNA is first separated from a sample. The isolation of total RNA may be carried out according to a general method known in the art (see Sambrook, J. et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001); Tesniere, C. et al., Plant Mol. Biol. Rep., 9:242(1991); Ausubel, F. M. et al., Current Protocols in Molecular Biology, John Willey & Sons (1987); and Chomczynski, P. et al., Anal. Biochem. 162:156(1987)). For example, TRIzol may be used to readily isolate total RNA in a cell. Next, cDNA is synthesized from the separated mRNA, and this cDNA is amplified. Since the total RNA of the present invention is isolated from a human sample, it has a poly-A tail at the end of the mRNA, and cDNA may be easily synthesized using oligo dT primer and reverse transcriptase by using such a sequence characteristic (see PNAS USA, 85:8998(1988); Libert F, et al., Science, 244:569(1989); and Sambrook, J. et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)). Subsequently, the synthesized cDNA is amplified through gene amplification reaction.
The primer used in the present invention is hybridized or annealed at one site of the template to form a double-stranded structure. Conditions for nucleic acid hybridization suitable for forming such a double-stranded structure are described in Joseph Sambrook et al., Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001) and Haymes, B. D., et al., Nucleic Acid Hybridization, A Practical Approach, IRL Press, Washington, D.C. (1985).
A variety of DNA polymerases may be used in the amplification of the present invention, and examples thereof include a Klenow fragment of E. coli DNA polymerase I, a thermostable DNA polymerase, and bacteriophage T7 DNA polymerase. Preferably, the polymerase is a thermostable DNA polymerase obtainable from a variety of bacterial species, and examples thereof include Thermus aquaticus(Taq), Thermus thermophilus(Tth), Thermus filiformis, Thermis flavus, Thermococcus literalis, and Pyrococcus furiosus(Pfu). When a polymerization reaction is performed, excess amounts of components needed for the reaction may be supplied to a reaction vessel. Excess amounts of components needed for amplification reaction refer to amounts to which the amplification reaction is not substantially restricted to concentrations of the components.
It is required to add a cofactor such as Mg2+, dATP, dCTP, dGTP, and dTTP to a reaction mixture to an extent to which a desired amplification degree can be achieved. All enzymes used in the amplification reaction may be active under the same reaction conditions. In fact, buffer enables all enzymes to have optimal reaction conditions. Thus, the amplification process of the present invention may be performed on a single reactant without changing conditions such as the addition of reactants.
In the present invention, annealing or hybridization is carried out under stringent conditions that allow specific binding between a target nucleotide sequence and a primer. The stringent conditions for annealing are sequence-dependent and vary according to environmental variables.
The term “amplification reaction” as used herein refers to a reaction for amplifying a nucleic acid molecule. Various amplification reactions have been reported in the art, and include polymerase chain reaction (hereinafter referred to as PCR) (U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159), reverse transcription-PCR (hereinafter referred to as RT-PCR) (Sambrook et al., Molecular Cloning. A Laboratory Manual, 3rd ed. Cold Spring Harbor Press (2001)), Miller, H. I. (WO 89/06700) and Davey, C. et al. (EP 329,822), ligase chain reaction (LCR) (17, 18), Gap-LCR (WO 90/01069), repair chain reaction (EP 439,182), transcription-mediated amplification (TMA) (19) (WO 88/10315), self-sustained sequence replication (20) (WO 90/06995), selective amplification of target polynucleotide sequences (U.S. Pat. No. 6,410,276), consensus sequence primed polymerase chain reaction (CP-PCR) (U.S. Pat. No. 4,437,975), arbitrarily primed polymerase chain reaction (AP-PCR) (U.S. Pat. Nos. 5,413,909 and 5,861,245), nucleic acid sequence based amplification (NASBA) (U.S. Pat. Nos. 5,130,238, 5,409,818, 5,554,517, and 6,063,603), strand displacement amplification, and loop-mediated isothermal amplification (LAMP), but the present invention is not limited thereto.
Other amplification methods that may be used are described in U.S. Pat. Nos. 5,242,794, 5,494,810, 4,988,617 and Ser. No. 09/854,317. In the most preferred embodiment of the present invention, the amplification process is performed according to polymerase chain reaction (PCR) disclosed in U.S. Pat. Nos. 4,683,195, 4,683,202, and 4,800,159.
PCR is the most well-known nucleic acid amplification method, and many variations and applications thereof have been developed. For example, touchdown PCR, hot start PCR, nested PCR, and booster PCR have been developed by modifying traditional PCR procedures to enhance the specificity or sensitivity of PCR. In addition, real-time PCR, differential display PCR (DD-PCR), rapid amplification of cDNA ends (RACE), multiplex PCR, inverse polymerase chain reaction (IPCR), vectorette PCR, thermal asymmetric interlaced PCR (TAIL-PCR), and multiplex PCR have been developed for specific applications. For more information on PCR, see McPherson, M. J., and Moller, S. G. PCR. BIOS Scientific Publishers, Springer-Verlag New York Berlin Heidelberg, N.Y. (2000), the teachings of which are incorporated herein by reference. The term “primer” as used herein refers to a single-stranded oligonucleotide capable of acting as a starting point of template-directed DNA synthesis under suitable conditions (i.e., four other nucleoside triphosphates and polymerase) in a suitable buffer at an appropriate temperature. The suitable length of the primer is typically 15-30 nucleotides, although it varies depending on various factors such as temperature and use of the primer. Short primer molecules generally require lower temperatures to form sufficiently stable hybrid complexes with the template.
The sequence of the primer does not need to have a sequence completely complementary to a partial sequence of the template, and it is sufficient when the sequence of the primer has sufficient complementary within a range that enables the primer to be hybridized with the template and implement its intrinsic function. Thus, a primer pair of the present invention does not need to have a sequence completely complementary to the sequence of the target gene as a template, and it is sufficient as long as it has sufficient complementary within a range that enables the primer pair to be hybridized with the sequence of the target gene to act as a primer. The primer of the present invention may be prepared with a sequence complementary to the mRNA (i.e., cDNA) sequence of the target gene. Design of such a primer may be easily carried out by those of ordinary skill in the art with reference to the cDNA sequence of the target gene.
cDNA of the amplified target gene is analyzed using a suitable method to examine the expression level of the gene. For example, the above-described amplification reaction product may be subjected to gel electrophoresis, and the resulting band may be observed and analyzed to examine the expression level of each gene. Through these amplification reactions, when the expression of each gene is higher than that of normal individuals, the possibility of developing into oral cancer or oral cancer may be predicted.
In addition, the possibility of developing into oral cancer or oral precancer may also be predicted by hybridization-based analysis using a probe hybridized to the target gene or cDNA thereof. The term “probe” as used herein refers to a single-stranded nucleic acid molecule and includes a sequence complementary to a target nucleic acid sequence. According to one embodiment of the present invention, the probe of the present invention may be modified within a range that does not impair an advantage of the probe, i.e., the improvement of hybridization specificity. Such a modification, i.e., labeling may provide a signal for detecting hybridization, which may be linked to an oligonucleotide. Suitable labels include, but are not limited to, fluorescent moieties (e.g., fluorescein), phycoerythrin, rhodamine, lissamine, Cy3 and Cy5 (Pharmacia), chromophores, chemiluminescent moieties, magnetic particles, radioactive isotopes (P32 and S35), mass labels, electron dense particles, enzymes (alkaline phosphatase or horseradish peroxidase), cofactors, substrates for enzymes, heavy metals (e.g., gold), antibodies, streptavidin, biotin, and hapten having a specific binding partner, such as digoxigenin and a chelating group. Labeling may be performed using various methods commonly used in the art, e.g., a nick translation method, a random priming method (Multiprime DNA labelling systems booklet, “Amersham” (1989)), and a carnation method (Maxam & Gilbert, Methods in Enzymology, 65:499(1986)). The label provides a signal that can be detected using fluorescence, radiation, coloring measurement, weight measurement, X-ray diffraction or absorption, magnetism, enzymatic activity, mass analysis, binding affinity, high frequency for hybridization, or nanocrystals.
According to one embodiment of the present invention, the probe of the present invention that is hybridized to target gene cDNA may be immobilized onto an insoluble carrier (e.g., a nitrocellulose or nylon filter, a glass plate, a silicon support, and a fluorocarbon support) to be prepared as a microarray. In the microarray, the probe of the present invention is used as a hybridizable array element. The immobilization onto the insoluble carrier is performed using a chemical bonding method or a covalent bonding method such as UV. For example, the hybridizable array element may bind to a glass surface modified to include an epoxy compound or an aldehyde group, and may also bind to a polylysine coating surface by UV. In addition, the hybridizable array element may be bound to a carrier via a linker (e.g., an ethylene glycol oligomer and a diamine). cDNA of each target gene may be obtained by the above-described process. The hybridization-based analysis may also be performed by labeling cDNA of the gene instead of using the probe. When the probe is used, the probe is hybridized with a cDNA molecule. In the present invention, suitable hybridization conditions may be determined through a series of procedures by an optimization procedure. For example, conditions such as temperature, the concentration of a component, hybridization and washing time, buffer components, and pH and ionic intensity thereof, and the like depend on various factors such as the length of a probe, GC content, a target nucleotide sequence, and the like. The detailed conditions for hybridization may be confirmed in Joseph Sambrook, et al., Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2001); and M. L. M. Anderson, Nucleic Acid Hybridization, Springer-Verlag New York Inc. N.Y. (1999). After the hybridization reaction, a hybridization signal generated through the hybridization reaction is detected. Hybridization signaling may be performed using various methods depending on the type of label bound to the probe. For example, when the probe is labeled with an enzyme, a substrate of the enzyme may be reacted with a hybridization reaction product to confirm the presence or absence of hybridization. Suitable combinations of enzyme/substrate include a peroxidase (e.g., horseradish peroxidase) and chloronaphthol, aminoethylcarbazole, diaminobenzidine, D-luciferin, bis-N-methylacridinium nitrate (lucigenin), resorufin benzyl ether, luminol, an Amplex red reagent (10-acetyl-3,7-dihydroxyphenoxazine), p-phenylenediamine-HCl and pyrocatechol (HYR), tetramethylbenzidine (TMB), 2,2′-Azine-di[3-ethylbenzthiazoline sulfonate] (ABTS), o-phenylene diamine (OPD), and naphthol/pyronine; alkaline phosphatase and bromochloroindolyl phosphate (BCIP), nitroblue tetrazolium (NBT), naphthol-AS-B1-phosphate and ECF substrate; glucose oxidase and nitroblue tetrazolium (t-NBT); and the like. When the probe is labeled with gold particles, this may be detected by a silver staining method using silver nitrate. By analyzing the intensity of the hybridizable signal by the above-described hybridization process, the possibility of developing into oral precancer or oral cancer may be predicted. That is, when a signal for cDNA of each target gene in a sample is stronger than an expression level thereof in normal individuals, the possibility of developing into oral precancer or oral cancer may be predicted.
The kit provided in the present invention may optionally include a reagent needed for performing target amplification PCR (e.g., PCR), such as buffer, a DNA polymerase cofactor, and deoxyribonucleotide-5-triphosphate. The kit of the present invention may also optionally include various polynucleotide molecules, reverse transcriptase, various buffers and reagents, and antibodies that inhibit DNA polymerase activity, which are needed for performing asymmetric PCR, and for melt curve analysis using a liquid-type array, the kit may also include lambda exonuclease, various buffers and reagents, and microwell plates.
In addition, in the kit, an optimal amount of a reagent used in a specific reaction may be easily determined by one of ordinary skill in the art that has acquired the teachings disclosed herein, and the kit may be designed as a separate package or compartment including the aforementioned components.
The present invention also provides a low molecular weight compound for inhibiting the expression of Axin2 and Snail that promotes cancer progression of precancerous lesions, thus effectively treating and preventing oral precancerous lesions and recurrent oral cancer that are characterized by repeated recurrence and field cancerization.
Therefore, in another embodiment, the present invention relates to a pharmaceutical composition for delaying or inhibiting the progression of oral precancerous lesions and recurrent oral cancer, which includes a compound for inhibiting the expression of the Axin2 gene or the Snail gene, as an active ingredient.
In another embodiment, the present invention relates to a method of treating oral precancer or recurrent oral cancer, which comprises administering a therapeutically effective amount of a compound for inhibiting the expression of the Axin2 gene or the Snail gene to an individual in need thereof. The compound for inhibiting the expression of the Axin2 gene or the Snail gene may be selected from the group consisting of niclosamide, 2′-hydroxycinnamaldehyde (HCA), 2′-benzoyloxycinnamaldehyde as a derivative of HCA, and a pharmaceutically acceptable salt thereof.
Niclosamide binds to GSK3 and thus inhibits the binding between GSK3 and Axin2, thereby degrading Snail, and inhibits epithelial-to-mesenchymal transition (EMT) and Wnt signaling (see
In one embodiment of the present invention, it was confirmed that, when YD-10B (CVCL-8929) and KB (CVCL 0372), which are oral cancer cell lines, and D38, which is an oral precancer cell line (McGregor F. et al., CANCER RESEARCH 62, 4757-4766, 2002), were treated with various concentrations of niclosamide, which is a compound for inhibiting the expression of the Axin2 gene or the Snail gene, the expression of Axin2 and Snail was inhibited in the YD-10B cell line, the KB cell line, and the D38 cell line (see
In another embodiment of the present invention, it was confirmed that, as a result of treating YD-10B and KB, which are oral cancer cell lines, and D38, which is an oral precancer cell line, with niclosamide and performing a migration assay thereon, the migration of oral precancer and cancer cells was inhibited in a manner dependent on the concentration of niclosamide used for treatment (see
In another embodiment of the present invention, it was confirmed that, as a result of treating the oral precancer cell line D38 with various concentrations of niclosamide for 72 hours and confirming apoptosis through a trypan exclusion assay, apoptosis occurred in a niclosamide-concentration-dependent manner (see
In another embodiment of the present invention, it was confirmed that, as a result of treating YD-10B and KB, which are oral cancer cell lines, and D38, which is an oral precancer cell line, with various concentrations of niclosamide, cell growth was inhibited as the concentration of niclosamide used for treatment was increased (see
In another embodiment of the present invention, to confirm the niclosamide treatment effect in a 3D culture model, as a result of treatment with 0.125 μM niclosamide when the oral precancer cell line D38 was cultured on a collagen sheet, it was confirmed that differentiation (*) of cells into keratinocytes was induced and that cell density was reduced by inhibiting cell proliferation, and while it was confirmed that the basal membrane was destroyed by D38 oral precancer cells in a non-treated control (red arrows), a smooth basal membrane was observed upon niclosamide treatment (blue arrows) (see
In another embodiment of the present invention, it was confirmed that, when the oral precancer cell line D38 and the oral cancer cell line YD10B were cultured on soft agar plates containing various concentrations of niclosamide, colony formation was inhibited in the oral precancer cell line and the oral cancer cell line according to the concentration of niclosamide used for treatment (see
In another embodiment of the present invention, the effect of niclosamide on the inhibition of oral cancer was confirmed in an animal model, and it was confirmed that, as a result of transplanting oral cancer cells YD10B (3×106 cells) to immunodeficient mice (Balb/c, athymic nude mice, NaraBiotech), dividing the mice into two groups, and then orally administering niclosamide to the two groups daily, the volume of tumors was reduced upon treatment with 200 mg/kg (mpk) of niclosamide (see
The term “treating” as used herein refers to, unless otherwise stated herein, reversing, alleviating, inhibiting the progression of, or preventing disorders or diseases to which the treatment is applied, or one or more symptoms of the disorders or diseases, and the term “treatment” as used herein refers to the act of treating when the term “treating” is defined as above.
In another embodiment, the present invention relates to a method of delaying or inhibiting the progression of oral precancerous lesions and recurrent oral cancer, including administering a compound for inhibiting the expression of the Axin2 gene or the Snail gene.
In another embodiment, the present invention relates to a use of a compound for inhibiting the expression of the Axin2 gene or the Snail gene for delaying or inhibiting the progression of oral precancerous lesions and recurrent oral cancer.
In another embodiment, the present invention relates to a use of a compound for inhibiting the expression of the Axin2 gene or the Snail gene in preparing a drug for delaying or inhibiting the progression of oral precancerous lesions and recurrent oral cancer.
In the present invention, the compound for inhibiting the expression of the Axin2 gene or the Snail gene may be selected from the group consisting of niclosamide, 2′-hydroxycinnamaldehyde (HCA), 2′-benzoyloxycinnamaldehyde (BCA) as a derivative of HCA, and a pharmaceutically acceptable salt thereof.
The composition of the present invention is prepared in the form of a solution, a powder, a gel, or a patch. When administered to a patient, precancerous lesions and recurrent oral cancer may be effectively controlled without side effects.
A carrier used in the pharmaceutical composition of the present invention includes a pharmaceutically acceptable carrier, an adjuvant, and a vehicle, and thus is collectively referred to as a pharmaceutically acceptable carrier. Examples of pharmaceutically acceptable carriers that may be used in the pharmaceutical composition of the present invention include, but are not limited to, ion exchange resins, alumina, aluminum stearate, lecithin, serum proteins (e.g., human serum albumin), buffer substances (e.g., various phosphates, glycine, sorbic acid, potassium sorbate, and partial glyceride mixtures of saturated vegetable fatty acids), water, salts or electrolytes (e.g., protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, and zinc salts), colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substrates, polyethylene glycol, sodium carboxymethylcellulose, polyarylates, waxes, polyethylene-polyoxypropylene-blocking polymers, polyethylene glycol, and lanolin.
Administration routes of the pharmaceutical composition according to the present invention include, but are not limited to, oral administration, intravenous administration, intramuscular administration, intraarterial administration, intramedullary administration, intrathecal administration, intracardiac administration, transdermal administration, subcutaneous administration, intraperitoneal administration, intranasal administration, intestinal administration, topical administration, sublingual administration, and intrarectal administration.
The administration routes may be oral administration and parenteral administration. The term “parenteral” as used herein includes subcutaneous, intradermal, intravenous, intramuscular, intraarticular, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.
The pharmaceutical composition may be in the form of a sterile injectable preparation, either as a sterile injectable aqueous or oil-based suspension. The suspension may be formulated according to techniques known in the art using a suitable dispersing or wetting agent (e.g., Tween 80) and a suspending agent. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent (e.g., a solution in 1,3-butanediol). Pharmaceutically acceptable vehicles and solutions may include mannitol, water, a Ringer's solution, and an isotonic sodium chloride solution. In addition, sterile nonvolatile oil is generally used as a solvent or a suspending medium. For this purpose, any nonvolatile oil with low irritation, including synthetic mono- or diglycerides may also be used. Fatty acids such as oleic acid and glyceride derivatives thereof are useful in injectable preparations as well as pharmaceutically acceptable natural oils (e.g., olive oil or castor oil), especially polyoxyethylated ones thereof.
The pharmaceutical composition of the present invention may be orally administered in any orally acceptable dosage form, by including, but being not limited to, capsules, tablets, and aqueous suspensions, and solutions. In the case of oral tablets, commonly used carriers include lactose and corn starch. Lubricants such as magnesium stearate are also typically added. For oral administration in a capsule form, useful diluents include lactose and dried corn starch. When the aqueous suspension is orally administered, the active ingredient is combined with an emulsifying agent and a suspending agent. If needed, a sweetening agent and/or a flavoring agent and/or a colorant may be added.
The pharmaceutical composition of the present invention may also be administered in the form of suppositories for rectal administration. These compositions may be prepared by mixing the compounds of the invention with suitable non-polar excipients which are solid at room temperature but liquid at rectal temperature. Such materials include, but are not limited to, cocoa butter, beeswax, and polyethylene glycols.
Oral administration of the pharmaceutical composition according to the present invention is particularly useful when desired treatment is associated with a site or organ that is accessible by topical application. When topically applied to the skin, the pharmaceutical composition should be formulated as a suitable ointment including the active ingredient suspended or dissolved in a carrier. Carriers for topical administration of the compound of the present invention include, but are not limited to, mineral oil, liquid paraffin, white Vaseline, propylene glycol, polyoxyethylene, polyoxypropylene compounds, emulsifying wax, and water. In other embodiments, the pharmaceutical composition may be formulated into suitable lotions or creams including an active compound suspended or dissolved in a carrier. Examples of suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl ester wax, stearyl alcohol, 2-octyldodecanol, benzyl alcohol, and water. The pharmaceutical composition of the present invention may also be topically applied in the form of rectal suppositories as a suitable enema to the lower intestinal tract. Topically applied transdermal patches are also included in the present invention.
The pharmaceutical composition of the present invention may be administered intranasally in the form of aerosols or inhaled. Such compositions may be prepared according to techniques well known in the art of pharmaceuticals and may be prepared as a solution in salt water using benzyl alcohol or other suitable preservatives, an absorption enhancer to enhance bioavailability, fluorocarbons, and/or other solubilizing or dispersing agents known in the art.
The compound of the present invention may be used in combination with a general anti-inflammatory agent or in combination with a matrix metalloproteinase inhibitor, a lipoxygenase inhibitor, and inhibitors of cytokines other than IL-113. The compound of the present invention may also be used in combination with immunomodulators (e.g., bropirimines, anti-human alpha interferon antibodies, IL-2, GM-CSF, methionine enkephalin, interferon alpha, diethyldithiocarbamate, tumor necrosis factor, naltrexone, and rEPO) or prostaglandins, to prevent or eradicate IL-1-mediated symptoms such as inflammation. When the compound of the present invention is administered in combination with other therapeutic agents, these may be sequentially or simultaneously administered to a patient.
The term “therapeutically effective amount” as used herein refers to a dosage level of about 1 mg/kg/day to about 100 mg/kg/day (typically, about 60 mg/patient/day to about 6 g/patient/day) to be used in treatment of the symptoms in humans.
The term “prophylactically effective amount” as used herein refers to a dosage level of about 0.1 mg/kg/day to about 100 mg/kg/day (typically, about 6 mg/patient/day to about 6 g/patient/day) to be used in prevention of the symptoms in humans.
However, it will be understood that a specific effective amount for a particular patient may vary depending on various factors, including the activity of particular compound used, age, body weight, general health conditions, gender, diet, administration time, administration routes, excretion rate, drug combination, and the severity of a particular disease to be prevented or treated. The pharmaceutical composition according to the present invention may be formulated into pills, sugar-coated tablets, capsules, liquids, gels, syrups, slurries, and suspensions.
In an exemplary embodiment, the pharmaceutical composition for oral administration may be prepared by mixing the active ingredient with solid excipients and may be prepared in the form of granules for preparation in the form of tablets or sugar-coated tablets. Suitable excipients include sugars such as lactose, sucrose, mannitol, and sorbitol or starches from corn, wheat flour, rice, potatoes, or other plants, cellulose such as methylcellulose, hydroxypropyl methyl cellulose, or sodium carboxymethylcellulose, carbohydrates or gelatin such as gums including gum arabic and gum tragacanth, or protein fillers such as collagen. If needed, disintegrating or solubilizing agents in the form of respective salts such as cross-linked polyvinylpyrrolidone, agar and alginic acid or sodium alginic acid may be added.
In an exemplary embodiment, for parenteral administration, the pharmaceutical composition of the present invention may be prepared as a water-soluble solution. Preferably, physically suitable buffer solutions such as Hank's solution, Ringer's solution, or physically buffered saline may be used. Water-soluble injection suspensions may include a substrate capable of increasing the viscosity of a suspension, such as sodium carboxymethylcellulose, sorbitol, or dextran. In addition, suspensions of the active ingredient may be prepared into suitable oily injection suspensions. Suitable lipophilic solvents or carriers include fatty acids such as sesame oil or synthetic fatty acid esters such as ethyl oleate, triglycerides, or liposomes. Polycationic non-lipid amino polymers may also be used as carriers. Optionally, the suspension may use a suitable stabilizing agent or drug to increase the solubility of the compound and to prepare a highly concentrated solution.
Hereinafter, the present invention will be described in further detail with reference to the following examples. It will be obvious to those of ordinary skill in the art that these examples are provided only to more particularly describe the present invention and are not intended to limit the scope of the present invention in accordance with the essence of the present invention.
Oral leukoplakia tissue samples used in the examples of the present invention were supplied from the pathology department of the dental hospital of Yonsei Medical Center, and oral submucous fibrosis tissue samples were supplied from the department of oral pathology of Peradeniya Dental University, Sri Lanka. Between 1995 and 2010, biopsy specimens were obtained from 223 patients with potentially malignant oral disorders (PMOD). Patients who were previously or concomitantly diagnosed with OSCC (n=16) or with tissues inappropriate for analysis (n=17) were excluded from the analysis. The analysis was performed on a total of 154 patients (96 males and 59 females; mean age of 55; age range between 13 years old and 89 years old) and 36 patients with oral submucous fibrosis (mean follow-up period: 6.4 years) (24 males and 12 females; mean age of 45; age range between 21 years old and 75 years old) (see
Characteristics of the tissue sample donors are shown in Table 1.
Oral leukoplakia and oral submucous fibrosis of sample slides were reviewed and diagnosed by pathologists. Normal oral mucosal tissues to be used as a normal control were supplied from 18 individuals with 3rd molar extraction (6 males and 12 females; mean age of 45; age range between 11 years old and 53 years old) and used. This analysis was carried out under the approval of the Research Advisory Committee (IRB 2-2013-0045) of the Dental College of Yonsei University.
To confirm the expression of Axin2 and Snail, immunohistochemical staining was performed as follows.
The tissue samples were deparaffinized with xylene and the alcohols were rehydrated, and then the tissue sections were allowed to react in a mixture of H2O2 and methanol diluted 1:40 at room temperature for 10 minutes to block endogenous peroxidase activity. Antigen retrieval was performed using a pressure-cooking (continuous cooking) method in antigen retrieval buffer (Dako, Glostrup, Denmark). After blocking with 5% bovine serum albumin at room temperature for 5 minutes, the sections were allowed to react at room temperature for 2 hours with a monoclonal rabbit anti-human Axin2 IgG (Abcam, Cambridge, UK) diluted at a ratio of 1:200 and monoclonal mouse anti-human Snail1 IgG (Abcam) diluted at a ratio of 1:500. A real envision HRP rabbit/mouse detection system (Dako) was used as a secondary antibody. The resulting sections were treated with 3,3′-diaminobenzidine, and then stained with hematoxylin. A negative control was treated with a rabbit anti-human IgG antibody (R&D Systems, Minneapolis, Minn., USA) or a mouse anti-human IgG (Dako) antibody as a primary antibody, and sections without positive cells were considered negative. SW480 cell blots were used as positive controls for both Axin2 and Snail1. In particular, the scaffolding protein Axin2 and the transcription factor Snail1 were found in the cytoplasm and nucleus, respectively. Axin2 immunoreactivity and Snail immunoreactivity were respectively divided into low and high Axin2 expression groups and low and high Snail expression groups due to the absence of the upper two thirds of the epidermis in the oral mucosa. Low expression indicates specimens expressing limited positively-stained cells in the lower one third of the epidermis or no positive cells, and high expression indicates specimens expressing benign cells of the upper two thirds of the epidermis. The results thereof are illustrated in
In addition, oral leukoplakia and oral submucous fibrosis showed different intracellular expression sites in terms of Snail expression. In the epithelium, Snail expression was shown only in the cytoplasm in the case of healthy individuals as a control, while Snail expression was shown in both in the nucleus and the cytoplasm in the case of 58 of 154 patients with oral leukoplakia (37.7%; P=0.001) and 13 of 36 patients with oral submucous fibrosis (36.1%; P=0.001) (See
Mucosal tissue expression of Axin2 and Snail in each of the tissue samples identified in Example 1 was compared using Fisher's exact test and a Chi-square test.
The correlation between Axin2 and Snail was analyzed using a Chi-square test.
All statistical analyses were performed using R package version 3.1.1 of the rms and eha libraries (The R Foundation for Statistical Computing, Vienna, Austria).
As a result, it was confirmed that none of the basic information of clinical factors including age, gender, and site was related to the expression of Axin2 and Snail in tissues of patients with oral leukoplakia and oral submucous fibrosis. In contrast, malignancy occurred more frequently in oral leukoplakia patients with tissues exhibiting high Snail expression compared to tissues exhibiting low Snail expression (40.7% versus 8.7%; P<0.001; see
No significant association was found between clinical parameters and tissue Axin2 expression in oral submucous fibrosis and oral leukoplakia. Nevertheless, Axin2 expression is significantly associated with Snail1 expression in oral leukoplakia (p=0.038) and oral submucous fibrosis (P=0.033) (See
Kaplan-Meier survival curves related to Axin2 expression and Snail expression were drawn, and the differences were analyzed by a log-rank test for the assessment of cancer-free survival in patients with oral leukoplakia. In addition, the intensity of association between malignancy of oral leukoplakia and various factors was evaluated using univariate and multivariate analyses using a Cox proportional hazards regression model. Variables with P<0.15 in the univariate analysis were included in the multivariate analysis, and data were expressed as odds ratios (ORs) and 95% confidence intervals (CI).
Kaplan-Meier analysis was used to estimate the cancer-free survival rates of oral leukoplakia patients. As a result, low survival rates were exhibited in elderly patients (survival period median-younger age—4427.5 days: older age—3,452 days; P=0.014) or high Snail expression cases (survival period median-low expression: 4,025 days-high expression: 3,589 days; P=0.005) (See
On the other hand, clinicopathologic variables of P<0.15 were considered to include multivariate analysis in univariate comparisons of patients with or without malignant mutation (See Table 4). In the univariate analysis, among factors including gender (P=0.086), age (P=0.019), Snail expression (P=0.007), and Axin2 expression (P=0.066), Cox regression analysis showed that gender (OR=3.13, 95% CI=1.27-7.73; P=0.014), age (OR=3.15, 95% CI=1.19-8.28; P=0.02), Snail expression (OR=4.41, 95% CI=1.78-10.93; P=0.001), and Axin2 expression (OR=7.47, 95% CI=2.23-25.02; P=0.001) were significantly associated with the risk of malignancy in oral leukoplakia patients.
In addition, risk factors associated with cancer-free survivability among patients with Snail-positive oral leukoplakia were analyzed. According to Kaplan-Meier analysis, patients with high Axin2 expression during the onset of illness had a low survival rate (survival period median: high Axin2 expression-374 days: low Axin2 expression-3,758 days; P<0.001 (See
Nomograms for predicting risk factors in the development of oral squamous cell carcinoma cells from leukoplakia lesions were created using selected important parameters and evaluated using a concordance index (c-index) and a calibration plot. P-values<0.05 were considered significant.
A nomogram was created to predict 5-year, 10-year, and 15-year cancer-free survival rates using clinical parameters and the expression of Axin2 and Snail1 (See
Measurement of the nomogram was performed to investigate the correlation between nomogram prediction and actual results in oral leukoplakia patients. For this, the x-axis represents a predicted value calculated by the nomogram, and the y-axis represents the actual likelihood of disease progression. An ideal nomogram will show a straight line of y=x indicating that the expected nomogram is completely consistent with actual clinical results. Drawing nomogram data results in a solid line reflecting a high level of predictability (See
In addition, the total points calculated in the nomogram are examined to evaluate characteristics of the predicted malignancy. The total points ranged from 0 to 365, and the patients were divided into three groups using a low quadrant value, i.e., 193, and a high quadrant value, i.e., 294. Thereafter, the Kaplan-Meier survival curves were drawn, and a log-rank test was performed (See
It was examined whether the expression of Axin2 and Snail cancer genes, which promote the cancer progression of precancerous lesions, is effectively inhibited when HCT116, SW480, SW620, and DLD-1 cells (ATCC, American Type Culture collection), which are colorectal cancer cell lines with high Axin2 expression, were treated with niclosamide, which is a low molecular weight compound that inhibits the expression of Axin2 and Snail, at an nM level.
As a result, as illustrated in
To confirm whether niclosamide is capable of inhibiting Axin-GSK3 interaction, cell lysates with full-length Axin2 were examined to perform immunoprecipitation experiments in the presence or absence of niclosamide.
An immunoprecipitation assay was performed as follows (Yook J I, et al. Nat Cell Biol. 8:1398-1406, 2006).
A doxycycline-induced His-tagged Axin2 expression vector was transfected into MCF-7 cells (ATCC, American Type Culture collection) and cultured, and a Triton X-100 lysate of whole cells was treated with Ni—Ti beads (Invitrogen) and niclosamide at each concentration to allow a reaction to occur therebetween. Proteins recovered in the beads were subjected to SDS-PAGE, followed by immunoblot analysis for GSK3, and a 1/20 volume of a control was added thereto.
As a result, as illustrated in
In the previously reported results of analyzing the structure of Axin-GSK3 binding, accumulation of the hydrophobic residues of Axin α-helix into a hydrophobic groove formed by the C-terminal loop of GSK3 is disclosed (Dajani R et al., EMBO J. 22:494-501, 2003), and thus the inventors of the present invention hypothesized that niclosamide would bind to the hydrophobic groove of GSK3 and interfere with the function of Axin. To verify this, in vitro analysis was designed to identify competitive inhibition of recombinant GSK3 binding to 19-mer FITC-conjugated Axin peptides by niclosamide.
Hig-tagged recombinant GSK3 beta was obtained from sf9 insect cells using a known method (Lee D G, et al. Nat Commun. 5:4423, 2014). The FITC-conjugated 19-mer Axin peptide (Axin1, 383-401, VEPQKFAEELIHRLEAVQR), which is known to bind to GSK3 as an amphipathic α-helix, was chemically synthesized (Peptron). To confirm competitive binding between the synthesized Axin peptide and niclosamide, His-tagged recombinant GSK3 and Ni—Ti beads were treated with niclosamide for 2 hours, and then washed three times with PBS, and quantitative fluorescence measurement was performed using Ni—Ti beads. Fluorescence intensity was represented in proportionate to the fluorescence intensity of a negative control from the 3rd experiment.
As a result, it was confirmed that the interaction between the recombinant GSK3 and the synthesized Axin peptide was inhibited in proportionate to the concentration of niclosamide added (See
Surface plasma resonance (SPR) analysis was performed to confirm whether niclosamide directly binds to GSK3. SPR was conducted using the ProteOn™ XPR36 Protein Interaction Array system (Bio-Rad Laboratories, Inc., CA, USA), and purified recombinant GSK3β, was immobilized to a ProteOn GLH sensor chip. Niclosamide or 19-mer wild type Axin peptide or mutant peptide (VEPQKAAEEAIHRAEAVQR, mutation underlined) were diluted by phosphate-buffered saline+Tween 20+1% DMSO at different concentrations and then flowed over the chip at a rate of 100 μl/min. The results thereof were analyzed by ProteOn Manager Software 2.0 using the standard Langmuir models for fitting kinetic data. The rate of complex formation was represented by the association constant (ka, in the unit of M-1s-1), and the rate of complex decay was represented by the dissociation constant (kd, in the unit of s-1), as given by Equation 1 below.
A high-affinity interaction is represented by a low dissociation constant, and rapid recognition and binding with interactants (rapid “on rate,” or high ka) and the stability of complex formation (slow “off rate,” or low kd) are as shown in the following equation: KD=kd/ka.
As a result, as illustrated in
In addition, molecular docking analysis was performed to structurally analyze the interaction between the Axin-binding site of GSK3 and niclosamide.
Molecular docking measurement was performed using the Maestro 10.4 molecular docking suite. The crystal structure of the human (pTyr216) GSK3β bound with an Axin peptide was measured the RCSB Protein Data Bank (PDB ID: 3ZDI). All water molecules and metal ions were removed, and hydrogen atoms were added to the protein, and the Epik module was used to add protons to ligand different from a sample at physiological pH. All compounds were energy-minimized using LigPrep and docked to receptor structures using the standard precision (SP) module of the Glide docking module within the Schrödinger Suite. Prior to Glide docking analysis a receptor grid box was generated at the centroid of co-crystallized ligands. Post-minimization was performed to optimize geometrical forms.
As a result, as illustrated in
According to the previous research results, it has been known that 2′-Hydroxycinnamaldehyde (HCA), which is a main component of cinnamon, and a derivative thereof, i.e., 2′-benzoyloxycinnamaldehyde (BCA) inhibit cancer metastasis through Snail expression inhibition by inhibiting LRP-1 receptors (Hwang H et al., J Neuroimmunol 2011, 230, 52-64; Ismail I A, et al., Breast Cancer Res Treat, 137, 697-708, 2013). Thus, to confirm whether HCA and BCA are capable of inhibiting Axin2 expression and Snail expression, colorectal cancer cells were treated with HCA and BCA, and it was examined whether Axin2 and Snail were expressed in a cell lysate. As HCA and BCA, those separated from cinnamon bark and purified were used (Hwang H et al., J Neuroimmunol 2011, 230, 52-64). As a result, as illustrated in
The expression of Axin2 and Snail was confirmed in a cell lysate after treating YD-10B (CVCL-8929) and KB (CVC_L 0372), which are oral cancer cell lines, and D38, which is an oral precancer cell line (McGregor F. et al., CANCER RESEARCH 62, 4757-4766, 2002), with various concentrations of niclosamide by using the same method of Example 5.
For the YD-10B and KB cell lines, a RPMI1640 medium containing 10% FBS and 1% penicillin/streptomycin was used. For the oral precancer cell line D38, a DMEM: F12 (3:1) medium containing 10% FBS and 1% penicillin/streptomycin was used. The respective cells were treated with niclosamide at the indicated concentration for 16 hours and the expression of Axin2 and Snail was analyzed through western blotting.
As a result, as illustrated in
Cell migration is regulated by Axin2 and Snail. In the present example, the YD-10B cell line, the KB cell line, and the oral precancer cell line D38 were treated with niclosamide, a migration assay was performed thereon, and then the cells were stained with crystal violet and cell migration values were measured.
As a result, as illustrated in
The oral precancer cell line D38 was treated with various concentrations of niclosamide for 72 hours and apoptosis was confirmed through a trypan exclusion assay.
As a result, as illustrated in
The oral cancer cell lines YD-10B and KB and the oral precancer cell line D38 were treated with various concentrations of niclosamide, and cell growth was measured by counting cells in real time.
From the results, as illustrated in
To confirm the niclosamide treatment effect in a 3D culture model, the results of treatment with 0.125 μM niclosamide when the oral precancer cell line D38 was cultured on a collagen sheet are illustrated in
From the results illustrated in
In addition, as illustrated in
The oral precancer cell line D38 and the oral cancer cell line YD10B were cultured on soft agar plates containing various concentrations of niclosamide. The corresponding concentration of niclosamide was administered while the respective cells were cultured on the soft agar plates for 3 weeks.
As a result, as illustrated in
To confirm the effect of niclosamide on the inhibition of oral cancer in an animal model, oral cancer cells YD10B (3×106 cells) were transplanted to immunodeficient mice (Balb/c, athymic nude mice, NaraBiotech), the mice were divided into two groups, and then niclosamide was orally administered to the two groups daily.
As a result, as illustrated in
According to the present invention, the possibility of developing malignancy such as into oral cancer from oral leukoplakia or oral submucous fibrosis with a white lesion in the mouth may be predicted and diagnosed, and thus the possibility of developing into oral precancer and oral cancer, which has no effective treatment method so far, is predicted early, thereby effectively removing the potential risk of oral cancer. The present invention also provides an oral therapeutic agent capable of controlling the progression and recurrence of precancerous lesions and the recurrence of oral cancer by providing drug information and effects for effectively controlling cancer genes that contribute to oral cancer malignancy, thus providing clinical benefits to patients.
While the present invention has been particularly shown and described with reference to specific embodiments thereof, it will be obvious to those of ordinary skill in the art that such specific embodiments are provided for illustrative purposes only and are not intended to limit the scope of the present invention. Therefore, the true scope of the present invention should be defined by the appended claims and equivalents thereto.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2017-0002869 | Jan 2017 | KR | national |
This is a continuation-in-part under 35 USC § 120 of International Patent Application PCT/KR2018/000395 filed Jan. 9, 2018, which in turn claims the priority under 35 USC § 119 of Korean Patent Application 10-2017-0002869 filed Jan. 9, 2017. The disclosures of International Patent Application PCT/KR2018/000395 and Korean Patent Application 10-2017-0002869 are hereby incorporated herein by reference, in their respective entireties, for all purposes.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/KR2018/000395 | Jan 2018 | US |
| Child | 16460992 | US |
