Patent Application
20240301506
This application incorporates by reference Sequence Listing XML submitted with this application and having the file name “80157US Sequence listing ST 26.xml” a creation date of 2024 Apr. 5 and a size of 26 kb.
The invention relates to a method for predicting prostate cancer metastasis by evaluating the expression of 8 specific genes in primary tumors of prostate cancer.
Prostate cancer (PCa) is the second leading cause of death from cancer in men in Chile and the world. According to the National Cancer Institute of the United States, deaths increase at an annual rate of 5.4%. The reason for this alarming growth is the lack of tools that allow the oncologist to predict which patients will develop a metastatic disease in order to intervene in a timely and appropriate manner. Thus, new and more effective methods are urged to predict the degree of aggressiveness of PCa, and thus determine which patients really require more aggressive treatments aimed at preventing the development of metastasis.
Research on the stromal role in the progression of PCa arises due to this need. The cancer cells are not isolated from their environment, but interact strongly with the tumor micro-structure or stroma, that is to say, the cells of the organ of origin of the tumor, in this case the prostate. The inventors have observed that the cells that accompany the tumor cells in the primary tumor, in this case in the prostate gland, participate in the ability of these to develop metastases.
Based on these important observations, the inventors developed the method of the invention, which allows for the evaluation of the degree of aggressiveness of PCa, studying prostatic stromal cells, specifically the pattern of expression of 8 specific genes.
In the state of the art there is no document that anticipates the method of the invention, although there are some similar approaches to the problem. For example, U.S.2011236903 A1 (MCCLELLAND MICHAEL et al, 2011 Sep. 29), suggests, especially in its claim 17, a prognostic method for a subject diagnosed with prostate cancer, comprising: (A) providing a sample of prostate tissue of said subject, wherein said sample comprises stromal cells of the prostate; (B) measuring the expression levels of one or more genes in said stromal cells, wherein said one or more genes are the prostate cancer signature genes; (C) comparing said measured expression levels to reference the expression levels of said one or more genes, wherein said reference expression levels are determined in non-cancerous prostate tissue stromal cells; and (D) if said measured expression levels are not significantly higher or lower than the reference expression levels, identify said subject with relatively better prognosis than if said measured expression levels are significantly higher or lower than the reference expression levels, or if said measured expression levels are significantly higher or lower than the reference expression levels, identify said subject as having a relatively worse prognosis than if said measured expression levels are not significantly higher or lower than the reference expression levels . . . Where the “prostate cancer signature” genes are chosen from Tables 3 and 4, where Table 3 describes 339 genes and Table 4 describes 146 genes. Where none of these 485 genes studied in this document coincide with the 8 genes studied in the present invention.
We also came across the International Publication WO2014052930 (A2) (MERCOLA DANIEL et al 2014 Apr. 3) that points to biomarkers for the diagnosis and prognosis of prostate cancer. In this document the expression of genes in tumor and stromal cells is studied, however, they select as biomarker the expression of 7 genes in tumor cells. That is to say, Mercola does not anticipate the method of the invention, and in addition the genes studied do not coincide with the genes of the invention.
The publication by Klein et al (European Urology 66 (2014) 550-560) discloses an assay of 17 genes to predict aggressiveness of prostate cancer. Where the authors identified 17 genes that represent multiple biological pathways that discriminate the aggressiveness of PCa in the tissue of the biopsy, despite tumor heterogeneity, multifocality and limited sampling at the time of biopsy. The authors do not directly correlate the studies of these genes with the development of metastasis. The 17 genes studied by Klein do not coincide with the genes studied in the present invention.
Erho et al (PLOS ONE 8(6): e66855) discloses a method for predicting prostate cancer metastasis by studying 22 markers in cancer cells of the primary tumor.
In this way the invention differs from what is known until now, and becomes the first diagnostic method that allows the formation of PCa metastasis to be predicted, becoming an invaluable tool when defining the most appropriate treatment for a patient with prostate cancer.
prostate stromal cells from patients without cancer (BAF), with non-metastatic cancer (CAF) and with metastatic cancer (mCAF).
The invention describes a method of prognosis (used interchangeably in this description as “prediction”) of metastasis in patients with prostate cancer, by studying the expression pattern of 8 specific genes: NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16, in PCa tumor stromal cells. Where, we conveniently study the expression of at least one of these 8 genes, or any of the possible combinations, of 2, 3, 4, 5, 6, 7 or the 8 genes identified by the inventors as markers of metastatic prostate cancer. Of these 8 biomarkers, the inventors have established that 7 of them have their expression increased in Metastatic Prostate Cancer, these are NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1; whereas GALNT16 decreases its expression in this type of cancer. In both cases the increase or decrease of the expression is established by comparing the level of expression of the same genes with the normal expression control condition. The normal expression control condition is the tissue expression of prostatic stroma without cancer. In another embodiment, the expression control condition is the normal expression in prostatic stromal tissue with non-metastatic cancer.
To determine the genes of the genetic signature of the invention, the inventors studied the expression of all genes in three types of samples, firstly, prostate stromal cells from patients without cancer (used interchangeably in this description as “without neoplasia”), what is known in the art as BAF (benign tissue associated fibroblast), secondly, in prostatic stroma of patients with non-metastatic cancer what is known in the art as CAF (carcinoma associated fibroblast) and thirdly, in prostatic stroma of patients with metastatic cancer, which is known in the art as mCAF (metastatic carcinoma associated fibroblast). Of the 30,000 genes studied, there were 16,955 that were expressed, and of these, the inventors were able to select 8 genes that have a differentiated expression in mCAF with respect to CAF and BAF, those which constitute the genetic signature of the present invention. The greater the dispersion between the gene expression data, the lower the statistical value of the result for a given gene, so the inventors discarded all those genes with a large dispersion in their expression in a given condition (BAF CAF or mCAF) and those with a similar expression pattern (low dispersion) were left. On the other hand, greater distance between the different groups on the vertical axis means that the expression values for that gene are statistically different in the groups compared. Therefore, the inventors selected as a second condition that there was, in addition to a low intra-group dispersion, a high inter-group differentiation. Therefore, it can be seen that mCAF samples have a dispersion by quantiles different from BAF or CAF, these last two present a similar dispersion. These results are shown in
As can be seen in
To develop the method of the present invention it is necessary first to obtain a sample of prostatic stroma. In an embodiment of the invention these samples are obtained from biopsies that are performed on patients with suspected cancer or already diagnosed with PCa, so that they would not mean an additional or different procedure from those usually performed for these patients. In another embodiment of the invention, a sample of prostatic stroma is obtained in a procedure additional to the biopsy that is performed on a patient with suspected cancer or already diagnosed with PCa. Although the method of the invention studies the expression of genes in the stroma, the analyses can be performed on complex samples with different cell types, containing stromal cells.
Thus, a preferred embodiment of the present invention comprises obtaining mRNA tissue from PCa primary tumors, and amplifying by RT PCR one or more of the genes chosen from NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16, and establishing the expression pattern of said genes. Where, if an overexpression of any of the genes NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1, or a decrease in the expression of GALNT16 is observed, this result is indicative of metastasis in patients with prostate cancer.
To establish the expression pattern of these genes, any method available in the art can be used at the time of performing the invention. If the gene product is RNA, it can be evaluated by microarray, SAGE, western blotting, RT-PCR, TRAC, quantitative PCR, multiplex qPCR or qNPA, or any other technique available at the time of performing the invention.
In a preferred embodiment the expression of the genes of the invention is established by Real Time PCR on the mRNA of the tissue sample.
In another preferred embodiment the expression of the genes of the invention is established by microarray on the mRNA of the tissue sample.
In another preferred embodiment the expression of the genes of the invention is established by multiplex qPCR on the mRNA of the tissue sample.
Donde esta diferencia para cualquiera de los genes o convenientemente todos ellos, incluyendo todas las posibles combinaciones son indicativos del desarrollo de una enfermedad metastásica.
In another embodiment of the invention the level of expression of the genes is determined by studying the proteins encoded by the genes NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16. Where the concentration of these proteins in the sample can be evaluated by ELISA, mass spectrometry, proteomic techniques, or immunohistochemistry, or any other technique available at the time of carrying out the invention. In each case the expression of the gene product, in this case proteins, of at least one of the genes NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16 should be compared with normal expression conditions, for example from patients without neoplasia (BAF) and establishing if there is an overexpression of the genes NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 or a silencing or diminution of expression of the GALNT16 gene. Where this difference for any of the genes or preferably all of them, including all possible combinations are indicative of the development of a metastatic disease.
In second place, the invention also describes a kit for predicting metastasis in prostate cancer by the method of the invention, where this kit comprises means for quantifying the expression products of the genes NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16, in a sample comprising prostatic tissue. The means provided in the kit comprise reagents, solutions and physical support elements. The reagents comprise, in a non-exclusive manner, any polypeptide or oligonucleotide for detecting the level of expression of genes and the solutions necessary to determine the level of expression of the genes in suitable equipment. In one embodiment, the kit of the invention comprises suitable reagents corresponding to specific antibodies for binding to proteins corresponding to any of the products of the expression of the NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16 genes. In another embodiment, the kit of the invention comprises suitable reagents corresponding to oligonucleotide sequences, such as specific primers or probes to hybridize to any of the products of the expression of the NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1, EBF1 and GALNT16. The solutions of the kit include the necessary solutions to determine the level of expression of the genes in suitable equipment. On the other hand, the means of physical support can be containers or tubes to contain the different reagents and solutions of the kit.
It is evident to the person skilled in the art that there are numerous PCR primers or probes that can be designed to perform these amplifications, and that the primers or probes used are not limiting for the embodiment of the invention. Both primers or probes described in the literature for these genes may be used or new primers or probes designed for this purpose, where all of these embodiments are within the scope of the present invention.
Prostate stromal cells were obtained from patients without evidence of neoplasia (BAF), from PCa primary tumors from patients who had developed clinical metastases (mCAF) and from patients with PCa who had not developed clinical metastasis (CAF). All these samples were obtained from puncture biopsies by means of tissue explants with the respective informed consent from the donors. Thirty samples were collected, 10 for each group.
The cells obtained were cultured in the laboratory until a critical number of them were obtained to carry out the studies.
To perform the gene expression experiments, mRNA was first extracted from each of the 30 samples (10 for each condition) with the Trizol reagent (Invitrogen) following the manufacturer's instructions. To determine the integrity of the extracted total RNA, a sample of it was subjected to electrophoresis in a 1% agarose gel stained with ethidium bromide. The RNA was quantified at 260 nm in a Nanodrop 1000 (Thermo).
Each sample was evaluated by a direct hybridization assay of only one color, using the Agilent Human Gene expression 4×44Kv2v system and runs in the iScan system. The gene expression data were analyzed by means of bioinformatics with the statistical program “R”.
Gene expression profiles were made by microarrays of these stromal cells for 30,000 genes in each case. The results indicate that the prostatic stroma in patients with metastatic PCa present gene expression profiles different from the prostatic stroma of patients without cancer or with non-metastatic PCa. From the 30,000 genes studied, 16,955 genes were found that were expressed in all groups; from these genes, a series of genes whose differential expression had a high degree of significance was first selected.
The results demonstrate that mCAFs stromal cell samples exhibit a differential gene expression profile, as compared to stromal samples of BAFs or CAFs. Among the differentially expressed genes, we established 8 that presented the greatest statistical difference between samples of patients with metastatic PCa versus benign samples or with PCa without metastasis. These results are schematized in
Primers for PCR (polymerase chain reaction) were designed for the genes identified in example 1, and 50 cases of patients without evidence of neoplasia (BAF), with PCa and clinical metastasis (mCAF) and with PCa without clinical metastasis were studied (CAF), through real-time PCR. The used primers are shown in Table 1.
In each case, a puncture biopsy was taken by means of tissue explants, from which a sample of total mRNA was obtained, which includes RNA from stromal cells and from tumor cells. Total RNA extraction was performed by a commercial kit (Qiagen) following the manufacturer's instructions. To determine the integrity of the extracted total RNA, a sample of it was subjected to electrophoresis in a 1% agarose gel stained with ethidium bromide. The RNA was quantified at 260 nm in a Nanodrop 1000 (Thermo).
As positive control of the reaction the 18S gene was quantified and to normalize the results based on the total amount of stroma of the sample, the messenger of Vimentina was quantified, the primers used in each case are also included in Table 1.
The obtained data corroborates that which was established in the microarrays of example 1, finding that when comparing the relative expression of these gene products in all cases there is a correlation between the overexpression of the NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1 and EBF1, and the decreased expression or silencing of GALNT16 and the clinical manifestations of these patients. That is to say, in the cases of patients with metastasis (mCAF) an increase in mRNA expression of NRP-1, MFAP4, NRIP3, THBS2, TNF, EDN1 and EBF1 is seen, and the decrease in the expression of GALNT16 mRNA, with respect to the expression in samples of patients without neoplasia (BAF) and with respect to the expression in samples of patients with non-metastatic prostate cancer.
From this result it can be determined that it is possible to clearly identify, by means of gene expression of stromal cells of the primary tumor, patients with metastatic prostate cancer.
It will be apparent to the person skilled in the art that it is possible to develop a kit for the method of the invention, including for example the PCR primers indicated in this example and the reagents needed to perform a real-time PCR, or any other mRNA quantitative technique or another product of expression of the genes of the invention. Likewise, it is possible to develop microarrays that determine the level of expression of these genes. Given that the genes are known and that the techniques for designing primers or probes are standardized in the art, the method of the invention can be performed with any pair of primers or probes that specifically amplify these genes, this not being a limitation of the method.
| Number | Date | Country | Kind |
|---|---|---|---|
| 3434-2016 | Dec 2016 | CL | national |
The present application is a Divisional of U.S. Ser. No . 16/474,459 filed Jun. 27, 2019 which is a 371 of International Patent Application No. PCT/CL2017/050095, filed on Dec. 29, 2017 which claims priority from Chilean Application 3434-2016 filed Dec. 30, 2016, the disclosures of which are incorporated in their entirety by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16474459 | Jun 2019 | US |
| Child | 18636932 | US |
