Patent Application
20110183864
The present invention provides method for the prognosis or detection of lung cancer, notably for early detection of lung cancer, as well as a kit and a (micro)array suitable for said method.
Lung cancer is the most frequent cause of cancer-related death in the western world, with only 15% of patients being alive 5 years after diagnosis (Jemal, A., et al., CA Cancer J Clin, 56:106-130 (2006)). This is almost exclusively due to a lack of approaches affording early diagnosis. About 75% of lung cancer patients present with advanced stage disease, without a chance for cure (Jemal, A., et al., CA Cancer J. Clin., 56:106-130 (2006)). Developing efficient tools for early detection thus represents the most promising strategy to improve prognosis of lung cancer (Mulshine, J. L. Nat. Rev. Cancer 3, 65-73 (2003)).
Numerous screening approaches have been tested over the last decades, including chest X-ray, sputum cytology, analysis of molecular markers and, more recently, annual spiral computed tomography (Bremnes, R. M., et al., C. Lung Cancer 49:1-12 (2005); (Henschke, C. I., et al., N. Engl. J. Med. 355:1763-1771 (2006)); (Bach, P. B. et al., D.C. Chest 123:72-82 (2003)). However, wide-spread application of these methods is encumbered by either limitations in sensitivity or specificity (sputum tests, chest x-ray) or feasibility and cost issues (spiral computed tomography). Recently, Spira and colleagues demonstrated the high power of gene expression profiling to detect lung cancer in surrogate tissue using bronchoscopically obtained epithelial cells derived from patients with early clinical symptoms (Spira, A., et al., Nature Medicine (2007)).
Nevertheless, an early diagnosis of lung cancer is still desirable.
It was now found that a particular blood-derived transcriptional signature is suitable to discriminate patients with lung cancer from non-affected smokers. When applied to blood samples from a prospective population-based cancer study, this signature accurately predicted the occurrence of lung cancer in smokers two years before the onset of clinical symptoms.
The invention thus provides
(1) method for the prognosis or early detection of lung cancer which comprises
(2) a preferred embodiment of the method of (1) above, wherein the determination is effected by a hybridization with probes specific for the nucleic acid sequences of SEQ ID NOs:2n (wherein n is an integer from 1 to 74), preferably said probes comprising the nucleic acid sequences of SEQ ID NOs:2n-1 (wherein n is an integer from 1 to 74);
(3) a hybridization (micro)array carrying probes for at least 25 indicator RNAs as defined in (2) above;
(4) a kit for the prognosis or detection of lung cancer according to the method of (1) or (2) above which comprises means for the determination of the expression rate of the indicator proteins as defined in (1) or (2) above or a (micro)array as defined in (3) above.
The (micro)array and kit of the invention are suitable as a screening tool to enable early diagnosis of lung cancer at a curable stage.
As transcriptional changes in peripheral blood were thought to be an early event in lung cancer development and might therefore be suitable to predict lung cancer before its clinical onset, a lung cancer associated “RNA-fingerprint” (Bild, A. H., et al. Nature 439:353-357 (2006)) was generated from peripheral blood samples obtained at diagnosis from 13 smokers with clinically manifest lung cancer (LC cases). Eleven of these 13 patients had been diagnosed with non-small cell lung cancer (NSCLC); the other 2 patients had a diagnosis of small-cell lung cancer (SCLC). Eleven samples from lung cancer-free smokers were used as controls (LC controls) (
Next, differentially expressed genes in blood samples before clinical onset of lung cancer in healthy smokers recruited in the European Prospective Investigation into Cancer and Nutrition (EPIC) were determined. This population-based cohort study prospectively investigates the natural history of more than 500,000 individuals from 10 European countries with 25,540 participants in the Heidelberg cohort. As part of this study, blood samples were routinely obtained from all individuals when entering the study. Within the EPIC-Heidelberg cohort 12 currently smoking individuals were identified, who had developed either NSCLC (n=7) or SCLC (n=5) within 24 months (median 14 months) post sampling (EPIC cases) with samples suitable for experimental evaluation (Table 2). These frequencies reflect the incidence of lung cancer among smokers within the Heidelberg cohort and are consistent with the inci-dence of lung cancer in Germany. Thirteen active smokers lacking a diagnosis of lung cancer within the total observation period following blood sampling were selected from the Heidelberg cohort based on matching of gender, age and smoking behaviour (EPIC controls) (Table 2). Differential gene expression in the EPIC cohort was assessed using the same ANOVA based filtering criteria (p<0.003). This set of genes robustly separated NSCLC, SCLC and controls within the EPIC group (NSCLC/SCLC p<0.05; case/control p<0.01) with a misclassification of two samples (20 and 23) (
When seeking for the predictive potential of the “RNA fingerprint” identified in the prevalent lung cancer cases, genes differentially expressed between NSCLC, SCLC and controls in clinical manifest lung cancer (LC group) were analyzed in order to evaluate whether the expression rate of said genes could be used to predict the clinical onset of lung cancer in the EPIC samples. First we used hierarchical clustering to group samples and detected significant clusters for cases and controls (p=0.01). For a sample clustered in the case group the odds ratio (OR) for developing lung cancer was estimated to be 10 [95% CI: 1.6 to 63]. We next built a predictor of lung cancer development by applying a K-nearest neighbor algorithm to the “RNA-fingerprint” (differentially expressed genes in the group with clinical manifest lung cancer (LC group)) and validated this predictor using leave-one-out-cross-validation (Table 3). Finally, when applying the resulting 65-feature predictor to the EPIC group, 80% of cases and controls were accurately classified (
In summary, by applying a blood-based lung cancer ‘RNA-fingerprint’ to blood samples obtained from incident lung cancer cases in the EPIC Heidelberg cohort, we were able to identify smokers who developed clinical symptoms of lung cancer within 2 years post blood sampling. These findings suggest that early tumor growth induces significant and measurable transcriptional changes in blood cells. We speculate that these changes are the result of a biological amplification of the ‘cancer signal’ by the immune system (Wang, X., et al. N. Engl. J. Med. 353:1224-1235 (2005)). Our findings imply that a blood-based gene-expression signature could be used for identification of patients at high risk for the onset of lung cancer that could be followed more stringently, e.g., by means of spiral computed tomography (Henschke, C. I., et al., N. Engl. J. Med. 355:1763-1771 (2006)). Such an integrated approach may afford early diagnosis of lung cancer at a curable stage of the disease.
Aspects (1) and (2) of the invention pertains to a method for the prognosis or detection of lung cancer (hereinafter shortly referred to as “method of the invention”), which comprises (a) determining the expression rates of at least 25 of the indicator RNAs represented by the nucleic acid sequences of SEQ ID NOs:2n (wherein n is an integer from 1 to 74), i.e. are selected from SEQ ID NOs:2, 4, 6, 8, 10 . . . 74, in a bodily fluid of the individual to be tested, and
The method of the invention is particularly suitable for early diagnosis of lung cancer.
A preferred embodiment of the method of the invention comprises determining the expression rates of at least 35, preferably at least 50, most preferably at least 70 of the indicator RNAs.
A further preferred embodiment of the method of the invention comprises determining the expression rate of at least the following indicator RNASs: SEQ ID NO: 25, 131, 17, 113, 13, 133, 43, 79, 53, 91, 103, 99, 1, 145, 5, 23, 101, 69, 73 and 141.
In still a further preferred embodiment of the method of the invention a deviation of the expression rate of at least 50%, preferably of at least 70% of the indicator RNAs is indicative for lung cancer or prognosis of lung cancer.
A “deviation of the expression rate” according to the method of the invention includes a decrease or an increase of the expression rate depending on the type of RNA as can be seen from Table 1, and a decrease or increase of at least 10% relative to the respective standard value is considered a significant event, i.e. a deviation of the expression rate.
It is particularly preferred that 30%, preferably 50% of the indicator RNAs, which are indicative with a decreased expression rate as shown in Table 1, show a decreased expression rate, and/or 30%, preferably 50% of the indicator RNAs, which are indicative with an increased expression rate as shown in Table 1, show an increased expression rate.
According to the method of the invention, the standard values of the expression rates are obtainable from a set of healthy patients (e.g. as a mean value) or via a standard mixture of the indicator RNAs. The latter may be generated according to the results from standard values of healthy patients.
According to the method of the invention, a bodily fluid includes blood, urine, sputum, saliva etc. Particular preferred is blood.
Further, in the method of the invention any RNA determination method for the determination of the expression rate available to the skilled person is applicable. A suitable method for the determination of the expression rate are RNA hybridization assays, particularly solid phase hybridization (micro)arrays.
Aspect (2) of the invention utilizes such hybridization assay with suitable probes for the indicator RNAs. It is preferred that said probes comprise 15 to 150, preferably 30 to 70 consecutive nucleotides of the nucleic acid sequences of SEQ ID NOs:2n (wherein n is an integer from 1 to 74). Alternatively the probes may comprise the nucleic acid sequences of SEQ ID NOs:2n-1 (wherein n is an integer from 1 to 74), i.e. are selected from SEQ ID NOs:1, 3, 5, 7, 9 . . . 73, preferably the probes are consisting of the nucleic acid sequences of SEQ ID NOs:2n-1 (wherein n is an integer from 1 to 74).
Aspect (3) of the invention pertains to hybridization (micro)array for the prognosis or detection of lung cancer carrying probes for at least 25 indicator RNAs, wherein said probes are as defined hereinbefore.
Aspect (4) of the invention pertains to a kit for the prognosis or detection of lung cancer according to the method of the invention, which comprises means for the determination of the expression rate of the indicator proteins as defined hereinbefore.
In particular the may comprise probes for said at least 25 indicator RNAs or a (micro)array of aspect (3) of the invention.
The kit may comprise further components suitable for performing the method of the invention, notably buffer, nucleotide solutions, markers/labels, standard solutions (including a standard mixture of the indicator RNAs as defined hereinbefore) etc.
The invention is described in more detail in the following examples which are however not to be construed as limiting the invention.
Recruitment of incident lung cancer cases in the EPIC-Heidelberg cohort: The European Prospective Investigation into Cancer and Nutrition (EPIC) is one of the largest epidemiological studies of diet and health. From 1993 to 1999 EPIC recruited 520.000 individuals aged over 20 years in 10 European countries. In Germany, 2 study centers (Heidelberg and Potsdam) contributed to EPIC. From all participants blood samples were collected at recruitment (Riboli, E., et al. Public health nutrition 5, 1113-1124 (2002)). Follow-up is still active and based on follow-up questionnaires, health insurance records and cancer and pathology registries. The participants of the EPIC Heidelberg cohort were drawn from a random sample of the general population of the Heidelberg area. All individuals entering the trial were healthy. 25540 individuals were recruited into this cohort between 1994 and 1998. A total of 21 incident lung cancer cases with a histologically proven diagnosis of lung cancer (according to ICD-10 (C34)) within the first two years of follow-up were identified within the EPIC-Heidelberg cohort. The incidence of lung cancer in the EPIC-Heidelberg cohort within these two years reflects the lung cancer incidence in Germany (men: EPIC Heidelberg 58/100,000, Germany 61.2/100,000; women: EPIC Heidelberg 26/100,000, Germany 20.8/100.000; Ferlay, J., et al. Ann Oncol 18, 581-592 (2007)). We excluded 1 case from the further analysis due to histology (neuroendocrine tumor). From the 20 individuals with non-small cell lung cancer (NSCLC) or small cell lung cancer (SCLC) 6 were not current smokers (1 never-smoker and 5 ex-smokers) and thus excluded from the analysis. Two further cases were excluded due to RNA of minor quality (EPIC-12 and EPIC-34). Twelve samples from current smokers with lung cancer (EPIC cases) with sufficient amounts of RNA in a quality passing our standard quality control filter were included for further analysis. The number of samples of never-smokers or ex-smokers within the EPIC Heidelberg cohort is too small to establish a distinct expression signature for this group. We did not conduct a joint expression analysis of smokers and non-smokers due to pronounced changes in RNA expression induced by smoking itself (unpublished results). EPIC controls were matched for age, gender and smoking behaviour (never-smoker, ex-smoker, smoker). All controls were free of lung cancer for the whole observation period (mean observation time 8.6 years). All individuals gave informed consent and the study was approved by the local ethics committee.
Recruitment of prevalent lung cancer cases in hospital-based patients: Prevalent lung cancer samples (LC cases) were recruited in the University Hospital Köln and the Lung Clinic Merheim, Köln, after informed consent and approval by the local ethics committee. In this cohort controls were defined as individuals without clinical manifest lung cancer at the time of blood asservation (LC controls). All individuals gave informed consent and the study was approved by the local ethics committee. All individuals were smokers
RNA extraction and array hybridization: We used snap frozen PBMC enriched blood (˜300 μl) from the EPIC study for RNA extraction. Blood samples were directly thawed in 5 ml of TRI Reagent BD (Molecular Research Center, Inc, USA). RNA was extracted according to the manufactures instruction and stored in 70% ethanol until finalization of preparation and dilution in H2O. For further RNA purification we applied Qiagen MinElute columns (Qiagen, Germany). By this method we extracted 960 ng RNA (mean; range 120-2500 ng). One sample contained no RNA. The OD ration 260/280 was 2.01 in mean (range 1.76-2.06). For the LC-group, we drew 2.5 ml blood directly into PAXgene vials providing stabilization of the gene expression profile. Samples were rested over night at room temperature and then stored at −80° C. until further preparation. RNA was extracted according to the manufactures instruction (Qiagen, Hilden, Germany). Biotin labeled cRNA preparation was performed using the Ambion® Illumina RNA amplification kit (Ambion, UK). Quality was controlled using a PCR based system (Zander, T. et al., J Med Biol Res 39, 589-593 (2006)). 1.5 μg biotin labeled cRNA was hybridized to Sentrix® whole genome bead chips 6×2 (Illumina, USA) and scanned on the IIlumina® BeadStation 500× (Debey, S., et al. Genomics 87, 653-664 (2006)). For data collection, we used Illumina® BeadStudio 1.4.0.2 software.
Bioinformatic tools: Primary expression data were extracted using BeadStudio software (Illumina, USA). Quantile normalization was performed using R-software (http://www.r-project.org/) (Boston, USA). To validate our predictor for future onset of lung cancer we performed a permutation analysis. For the permutation analysis the classes of samples in the group of prevalent lung cancer and controls were randomly assigned leading to new “randomized” datasets. For each randomised data set we generated a new “RNA fingerprint” based on differentially expressed genes (ANOVA p=0.003) in the group of prevalent lung cancer (LC group). We then used this new “RNA-fingerprint” to predict samples from individuals with future onset of lung cancer (EPIC group). The odds ratio was calculated without inclusion of covariables (Bland, J. M. & Altman, B M J, Clinical research ed 320, 1468 (2000)).
Quality control of microarrays: Quality control was crucial for samples of the group of EPIC cases and controls, that were stored as whole blood and frozen without RNA stabilization. We performed quality control by visual inspection of the distribution of raw expression values. In addition, the absolute deviation of each array from the overall median was determined. In short, the median expression value for each array was calculated. Next the median of these median expression values (overall median) was taken and the deviation of each array median from the overall median was determined (analogous to probe outlier detection used by Affymetrix before expression value calculation (Affymetrix. http://www.affymetrix.com/support/technical/whitepapers/sadd whitepaper.pdf(2002)). When plotting the deviations (
Description of the generation of the gene-list: Oligos were selected as described in the paper and supplements. Briefly, RNA was extracted from PBMC enriched frozen blood samples for the incident cases and from PAXgene stabilized blood samples for the prevalent samples by the technique as described in the supplement. cRNA was generated and labelled and arrays were hybridized as described in supplemental methods. Primary expression data were extracted using Bead-Studio software (Illumina). Further primary expression data were quantile normalized. Low quality samples were extracted by measuring the deviation from the median expression value. The cut-off value was set at 28. High quality samples were used for further analysis. Then transcripts which are significantly different between NSCLC, SCLC and controls were identified by ANOVA test with a p-value of <0.003 in samples from patients with prevalent lung cancer compared to controls. The transcripts matching these criteria were selected by the dCHIP software. In a next step only these selected transcripts are used to classify cases and controls within a group of samples with incident lung cancer and controls. In a following step those Oligos specific for the transcripts matching the above mentioned criteria and further being identical on the Illumina platform WG6 VS1 and WG6 VS2 were identified by BLAST analysis. WG6 VS1 is no longer available and reproduction of results was performed on WG6 VS2. These Oligos were then blasted against the human genome and the RefSeq sequence with the highest homology was taken and the FASTA sequence for the respective transcript is given.
For a test this implies that the expression of the transcripts within the list have to be measured in peripheral blood. The complex expression pattern of these transcripts can be then used to identify cases as it is significantly different.
Characteristics of the prevalent hospital-based lung cancer cases and controls (LC group): For each blood sample in the (prevalent) group of LC controls and cases gender, smoking behaviour, age, histology and clinical stage of lung cancer at diagnosis is given. All blood samples from cases derive from patients with known diagnosis of lung cancer are summarized in the following Table 2.
Characteristics of the incident lung cancer cases and controls in the EPIC cohort (EPIC-group): For each blood sample from the EPIC-Heidelberg cohort (incident cases and controls) gender, smoking behaviour, age, histology, clinical stage of lung cancer at diagnosis and time between blood sampling and clinical manifestation of lung cancer is given in Table 3 below.
Characteristics of the predictive genes identified in the LC group: Using an ANOVA test (3 groups: NSCLC, SCLC and controls) 151 differentially expressed transcripts were identified (p-value<0.003) in the LC group. We used this set of genes as the lung cancer specific “RNA fingerprint” (Bild, A. H., et al. Nature 439, 353-357 (2006)). To predict incident lung cancer cases within the EPIC group we built a predictor using a KNN algorithm (GenePattern). For validation of this predictor a leave-one-out-cross-validation was performed. The results are summarized in the attached Table 4. In detail, the probe names of the transcripts used for the predictor, the gene symbol (if available) and the accession number (if available) are given. Furthermore, the p-value determined in the former ANOVA test is given. The right column indicates the number of arrays for which the respective probe was used as a predictive feature.
Blood samples from the EPIC cohort were not taken explicitly for RNA analysis. No stabilization was performed. Blood samples were taken and centrifuged in straws. PBMC enriched fractions (5 mm) of the straw were taken for further analysis.
Blood Collection using PAX Gene System
The PAXgene system was used for prevalent lung cancer samples. It allows standardized and easy blood collection based on convenient BD Vacutainer™ technology. The PAXgene tube contains a proprietary reagent that immediately stabilizes intracellular RNA for 3 days at room temperature (18-25° C.) and 5 days at 2-8° C. (Rainen, L., et al., Clin Chem 48, 1883-1890 (2002)). The here described protocol is extracted from the manufacturer's instructions.
Ensure that the PAXgene Blood RNA Tube is at room temperature (18° C.-25° C.) prior to use and properly labeled with patient identification.
If the PAXgene Blood RNA Tube is the only tube to be drawn, a small amount of blood should be drawn into a “Discard Tube” prior to drawing blood into the PAXgene Blood RNA Tube. Otherwise, the PAXgene Blood RNA Tube should be the last tube drawn in the phlebotomy procedure.
Using a BD Vacutainer® Safety-Lok™ Blood Collection Set, collect blood into the PAXgene Blood RNA Tube holding the PAXgene Blood RNA Tube vertically, below the blood donor's arm, during blood collection.
Allow at least 10 seconds for a complete blood draw to take place. Ensure that the blood has stopped flowing into the tube before removing the tube from the holder.
Gently invert the PAXgene Blood RNA Tube 8 to 10 times.
Store the PAXgene Blood RNA Tube upright at room temperature (18° C.-25° C.) for at least 2 h. After 24 h proceed to RNA isolation or store at −20° C. or −80° C. for long-term storage.
To freeze PAXgene™ Blood RNA Tubes stand them upright in a wire rack. Do not freeze tubes upright in a Styrofoam tray as this may cause the tubes to crack. Tubes can be stored at −20° C. and below. If tubes are to be frozen at temperatures below −20° C., freeze the tubes first at −20° C. for 24 hours, then transfer them to −70° C. or −80° C.
To thaw PAXgene™ Blood RNA Tubes, place them in a wire rack at ambient temperature (18-22° C.) for approximately two hours. Do not thaw PAXgene™ Blood RNA Tubes at temperatures above 22° C. One suggestion is to remove the tubes from the freezer the afternoon before processing, thaw overnight, and process tubes the next day. After thawing, carefully invert the tubes 10 times before starting RNA preparation.
Homogenization: Homogenize blood samples in TRI Reagent (5 ml/5 mm straw) by directly thawing sample in TriReagent. Rapidely homogenize by mechanically pipetting samples several times. Thorough pipetting is important and coagulation of samples must be avoided
Phase separation: Store the homogenate for 5 minutes at room temperature to permit the complete dissociation of nucleoprotein complexes. Next, supplement the homogenate with 0.2 ml chloroform per 1 ml of TRI Reagent, cover the samples tightly and shake vigorously for 15 seconds. Store the resulting mixture at room temperature for 2-15 minutes and centrifuge at 12,000 g for 15 minutes at 4 C. Following centrifugation, the mixture separates into a lower red phenol-chloroform phase, interphase and the colorless upper aqueous phase. RNA remains exclusively in the aqueous phase whereas DNA and proteins are in the interphase and organic phase. The volume of the aqueous phase is about 60% of the volume of TRI Reagent used for homogenization. Chloroform used for phase separation should not contain isoamyl alcohol or any other additive.
RNA Prcipitation: Transfer the aqueous phase to a fresh. Precipitate RNA from the aqueous phase by mixing with isopropanol. Use 0.5 ml of isopropanol per 1 ml of TRI Reagent used for the initial homogenization. Store samples at room temperature for 5-10 minutes and centrifuge at 12,000 g for 8 minutes at 4-25 C. RNA precipitate (often invisible before centrifugation) forms a gel-like or white pellet on the side and bottom of the tube.
RNA wash: Remove the supernatant and wash the RNA pellet (by vortexing) with 70% ethanol and subsequent centrifugation at 7,500 g for 5 minutes at 4-25 C. Add at least 1 ml of 70% ethanol per 1 ml TRI Reagent used for the initial homogenization. Samples were stored in 70% ethanol prior further clean-up.
RNA solubilization: Remove the ethanol wash and briefly air-dry the RNA pellet for 3-5 min. Ad the desired amount of RNAse free water.
RNA Clean-Up using RNeasey MinElute Kit (Qiagen):
Adjust the sample to a volume of 100 μl with RNase-free water. Add —350 μl Buffer RLT, and mix well. If starting with an RNA pellet, be sure that the pellet is dissolved in the RNase-free water (supplied) before adding Buffer RLT.
Add 250 μl of 96-100% ethanol to the diluted RNA, and mix well by pipetting. Do not centrifuge. Proceed immediately to next step.
Transfer the sample (700 μl) to an RNeasy MinElute spin column placed in a 2 ml collection tube (supplied). Close the lid gently, and centrifuge for 15 s at 8000×g. Discard the flow-through.
Place the RNeasy MinElute spin column in a new 2 ml collection tube (supplied). Add 500 μl Buffer RPE to the spin column. Close the lid gently, and centrifuge for 15 s at 8000×g to wash the spin column membrane. Discard the flow-through. Note: Buffer RPE is supplied as a concentrate. Ensure that ethanol is added to Buffer RPE before use.
Add 500 μl of 80% ethanol to the RNeasy MinElute spin column. Close the lid gently, and centrifuge for 2 min at 8000×g to wash the spin column membrane. Discard the flow-through and collection tube.
Place the RNeasy MinElute spin column in a new 2 ml collection tube (supplied). Open the lid of the spin column, and centrifuge at full speed for 5 min. Discard the flow-through and collection tube. It is important to dry the spin column membrane since residual ethanol may interfere with downstream reactions.
Place the RNeasy MinElute spin column in a new 1.5 ml collection tube (supplied). Add 14 μl RNase-free water directly to the center of the spin column membrane. Close the lid gently, and centrifuge for 1 min at full speed to elute the RNA.
RNA Preparation after PAXgene Asservation:
The PAXgene Blood RNA Kit allows the isolation of total RNA from 2.5 ml human whole blood collected in the PAXgene Blood RNA Tube. The here described protocol is extracted from the manufacturer's instructions with slight modifications.
Centrifuge the PAXgene Blood RNA Tube for 10 minutes at 3000-5000×g at room temperature using a swing out rotor. Important: The rotor must contain tube adapters for round-bottom tubes. If other types of tube adapter are used, the tubes may break during centrifugation.
Remove the supernatant by decanting or pipetting. Add 5 ml RNase-free water to the pellet, and close the tube using a fresh secondary Hemogard closure. If the supernatant is decanted, take care not to disturb the pellet, and dry the rim of the tube with a clean paper towel.
Vortex until the pellet is visibly dissolved, and centrifuge for 10 minutes at 3000-5000×g using a swing-out rotor. Remove and discard the entire supernatant. Small debris remaining in the supernatant after vortexing but before centrifugation will not affect the procedure. Important: Incomplete removal of the supernatant will inhibit lysis and dilute the lysate, and therefore affect the conditions for binding RNA to the PAXgene membrane.
Thoroughly resuspend the pellet in 360 μl Buffer BR1 by vortexing.
Pipet the sample into a 1.5 ml microcentrifuge tube. Add 300 μl Buffer BR2 and 40 μl proteinase K. Mix by vortexing for 5 seconds, and incubate for 15 minutes at 55° C. using a shaker-incubator at 1400 rpm. After incubation, set the temperature of the shaker-incubator to 65° C. (for step 20). Important: Do not mix Buffer BR2 and proteinase K together before adding them to the sample. See Note 1.
Centrifuge for 5 min at maximum speed in a microcentrifuge. Transfer the supernatant to a fresh 2 ml microcentrifuge tube. A minimum g-force of 10,000×g is required. Transfer of small debris remaining in the supernatant after centrifugation at full speed will not affect the procedure. See Note 2.
Add 350 μl abs. ethanol. Mix by vortexing, and centrifuge briefly (1-2 seconds at 500-1000×g) to remove drops from the inside of the tube lid. Important: The length of the centrifugation must not exceed 1-2 seconds, as this may result in pelleting of nucleic acids and reduced yields of total RNA.
Pipet 700 μl sample into the PAXgene RNA spin column (red) placed in a 2 ml processing tube, and centrifuge for 1 minute at 8000-20,000×g. Place the spin column in a new 2 ml processing tube, and discard the old processing tube containing flow-through.
Pipet the remaining sample into the PAXgene RNA spin column, and centrifuge for 1 minute at 8000-20,000×g. Place the spin column in a new 2 ml processing tube, and discard the old processing tube containing flow-through. Important: Carefully pipet the sample into the spin column and visually check that the sample is completely transferred to the spin column. See Note 3.
Pipet 350 μl Buffer BR3 into the PAXgene RNA spin column. Centrifuge for 1 minute at 8000-20,000×g. Place the spin column in a new 2 ml processing tube, and discard the old processing tube containing flow-through.
Add 10 μl DNase I stock solution to 70 μl Buffer RDD in a 1.5 ml microcentrifuge tube. Mix by gently flicking the tube, and centrifuge briefly to collect residual liquid from the sides of the tube. If processing, for example, 10 samples, add 110 μl DNase I stock solution to 770 μl Buffer RDD. Important: DNase I is especially sensitive to physical denaturation. Mixing should only be carried out by gently flicking the tube. Do not vortex.
Pipet the DNase I incubation mix (80 μl ) directly onto the PAXgene RNA spin column membrane, and place on the benchtop (20-30° C.) for 15 minutes. Important: Ensure that the DNase I incubation mix is placed directly onto the membrane. DNase digestion will be incomplete if part of the mix is applied to and remains on the walls or the O-ring of the spin column.
Pipet 350 μl Buffer BR3 into the PAXgene RNA spin column, and centrifuge for 1 minute at 8000-20,000×g. Place the spin column in a new 2 ml processing tube, and discard the old processing tube containing flow-through.
Pipet 500 μl Buffer BR4 to the PAXgene RNA spin column, and centrifuge for 1 minute at 8000-20,000×g. Place the spin column in a new 2 ml processing tube, and discard the old processing tube containing flow-through. Important: Buffer BR4 is supplied as a concentrate. Ensure that ethanol is added to Buffer BR4 before use.
Add another 500 μl Buffer BR4 to the PAXgene RNA spin column. Centrifuge for 3 minutes at 8000-20,000×g.
Discard the tube containing the flow-through, and place the PAXgene RNA spin column in a new 2 ml processing tube. Centrifuge for 1 minute at 8000-20,000×g.
Discard the tube containing the flow-through. Place the PAXgene RNA spin column in a 1.5 ml microcentrifuge tube, and pipet 40 μl RNAse-free water directly onto the PAXgene RNA spin column membrane. Centrifuge for 1 minute at 8000-20,000×g to elute the RNA. It is important to wet the entire membrane with H2O in order to achieve maximum elution efficiency.
Repeat the elution step as described, using the same 40 μl RNAse-free water and the same microcentrifuge tube.
Incubate the eluate for 5 minutes at 65° C. in the shaker-incubator without shaking. After incubation, chill immediately on ice. Important: This incubation at 65° C. denatures the RNA for downstream applications. Do not exceed the incubation time or temperature.
If the RNA samples will not be used immediately, store at −20° C. or −70° C. Since the RNA remains denatured after repeated freezing and thawing, it is not necessary to repeat the incubation at 65° C.
The concentration of RNA should be determined by measuring the absorbance at 260 nm (A260) in a spectrophotometer. To ensure significance, readings should be greater than 0.15. An absorbance of 1 unit at 260 nm corresponds to 44 μg of RNA per ml (A260=1, c=44 μg/ml). This relation is valid only for measurements in 10 mM Tris·Cl, pH 7.5. Therefore, if it is necessary to dilute the RNA sample, this should be done in 10 mM Tris·Cl.
The ratio of the readings at 260 nm and 280 nm (A260/A280) provides an estimate of the purity of RNA with respect to contaminants that absorb in the UV, such as protein. However, the A260/A280 ratio is influenced considerably by pH. Lower pH results in a lower A260/A280 ratio and reduced sensitivity to protein contamination. For accurate values, we recommend measuring absorbance in 10 mM Tris·Cl, pH 7.5. Pure RNA has an A260/A280 ratio of 1.9-2.1 in 10 mM Tris·Cl, pH 7.5. Always calibrate the spectrophotometer with the same solution.
The integrity and size distribution of total RNA purified using the PAXgene Blood RNA System can be checked by denaturing agarose gel electrophoresis (1% w/v) and ethidium bromide staining. The respective ribosomal bands should appear sharp on the stained gel. 28S ribosomal RNA (5 kb) bands should be present with an intensity approximately twice that of the 18S RNA (1.9 kb) band. If the ribosomal bands in a given lane are not sharp, but appear as a smear of smaller sized RNAs, it is likely that the RNA sample suffered major degradation during preparation. Only RNA samples of good purity and integrity should be used for further microarray analysis.
cDNA and cRNA synthesis using Illumina TotalPrep RNA Amplification Kit: RNA amplification has become the standard method for preparing RNA samples for array analysis (Kacharmina, J. E., et al., Methods Enzymol 303, 3-18 (1999); 3. Pabon, C., et al., Biotechniques 31, 874-879 (2001)). The Illumina® TotalPrep RNA Amplification Kit is a complete system for generating biotinylated, amplified RNA for hybridization with Illumina Sentrix® arrays. It is based on the RNA amplification protocol developed in the laboratory of James Eberwine Van Gelder, R. N., et al., Proc Natl Acad Sci U S A 87, 1663-1667 (1990)). The procedure consists of reverse transcription with an oligo(dT) primer bearing a T7 promoter using Array-Script™, a reverse transcriptase (RT) engineered to produce higher yields of first strand cDNA than wild type enzymes. ArrayScript catalyzes the synthesis of virtually full-length cDNA. The cDNA then undergoes second strand synthesis and clean-up to become a template for in vitro transcription with T7 RNA Polymerase where hundreds to thousands of biotinylated, antisense RNA copies are synthesized of each mRNA in a sample. The labeled cRNA produced with the kit was developed for hybridization with Illumina arrays. The here described protocol is according to the manufacturer's instructions.
Reverse Transcription to Synthesize First Strand cDNA:
Place a maximum volume of 11 μl of total RNA (100 ng) into a nonstick, sterile, RNase-free, 0.2 ml microcentrifuge tube.
Add Nuclease-free Water as necessary to bring all samples to 11 μl.
At room temperature, prepare Reverse Transcription Master Mix in a nuclease-free tube. Assemble enough to synthesize first strand cDNA from all the RNA samples in the experiment. Reverse Transcription Master Mix (for a single 20 μl reaction); 1 μl T7 Oligo(dT) Primer (17-21dT); 2 μl 10× First Strand Buffer; 4 μl dNTP Mix; 1 μl RNase Inhibitor and 1 μl ArrayScript.
Mix well by gently vortexing. Centrifuge briefly (˜5 sec) to collect the Reverse Transcription Master Mix at the bottom of the tube and place on ice.
Transfer 9 μl of Reverse Transcription Master Mix to each RNA sample. Mix thoroughly by pipetting up and down 2-3 times, then flicking the tube 3-4 times, and centrifuge briefly to collect the reaction in the bottom of the tube.
Place the samples in a 42° C. incubator. Incubate reactions for 2 h at 42° C.
After the incubation, centrifuge briefly (˜5 sec) to collect the reaction mixture at the bottom of the tube. Place the tubes on ice and immediately proceed Second Strand cDNA Synthesis.
Second Strand cDNA Synthesis:
On ice, prepare a Second Strand Master Mix in a nuclease-free tube in the order listed below. Assemble enough to synthesize second strand cDNA from all the samples in the experiment.
Assemble the Second Strand Master Mix on ice in the order shown: Second Strand Master Mix (for a single 100 μl reaction); 63 μl Nuclease-free Water; 10 μl 10× Second Strand Buffer; 4 μl dNTP Mix (2 mM dATP, dTTP, dCTP and dGTP); 2 μl DNA Polymerase; and 1 μl RNase H.
Mix well by gently vortexing. Centrifuge briefly (˜5 sec) to collect the mixture at the bottom of the tube and place on ice.
Transfer 80 μl of Second Strand Master Mix to each sample. Mix thoroughly by pipetting up and down 2-3 times, then flicking the tube 3-4 times, and centrifuge briefly to collect the reaction in the bottom of the tube.
Place the tubes in a 16° C. thermal cycler. It is important to cool the thermal cycler block to 16° C. before adding the reaction tubes because subjecting the reactions to temperatures >16° C. will compromise cRNA yield. Incubate 2 h in a 16° C. thermal cycler.
After the 2 h incubation at 16° C., place the reactions on ice and proceed to cDNA Purification (below), or immediately freeze reactions at −20° C. Do not leave the reactions on ice for more than 1 h.
This is a potential overnight stopping point (at −20° C.), but it is better to complete the cDNA purification before stopping.
cDNA Purification
Preheat Nuclease-free Water to 50-55° C.
Check the cDNA Binding Buffer for precipitation before using it. If a precipitate is visible, redissolve it by warming the solution to 37° C. for up to 10 min and vortexing vigorously. Cool to room temp before use.
Add 250 μl of cDNA Binding Buffer to each sample, and mix thoroughly by pipetting up and down 2-3 times, then flicking the tube 3-4 times. Follow up with a quick spin to collect the reaction mixture in the bottom of the tube. Proceed quickly to the next step.
Check that the cDNA Filter Cartridge is firmly seated in its wash tube (supplied).
Pipet the cDNA sample/cDNA Binding Buffer onto the center of the cDNA Filter Cartridge.
Centrifuge for ˜1 min at 10,000×g, or until the mixture is through the filter. Discard the flow-through and replace the cDNA Filter Cartridge in the wash tube.
Apply 500 μl Wash Buffer to each cDNA Filter Cartridge.
Centrifuge for ˜1 min at 10,000×g, or until all the Wash Buffer is through the filter.
Discard the flow-through and spin the cDNA Filter Cartridge for an additional minute to remove trace amounts of Wash Buffer.
Transfer cDNA Filter Cartridge to a cDNA Elution Tube.
Elute cDNA with a total of 19 μl 50-55° C. Nuclease-free Water. It is important to use Nuclease-free Water that is at 50-55° C. for the cDNA elution. Colder water will be less efficient at eluting the cDNA, and using hotter water (≧58° C.) may result in reduced cRNA yield.
Apply 10 μl of Nuclease-free Water (preheated to 50-55° C.) to the center of the filter in the cDNA Filter Cartridge.
Leave at room temperature for 2 min and then centrifuge for ˜1.5 min at 10,000×g, or until all the Nuclease-free Water is through the filter.
Apply a second aliquot of 9 μl preheated Nuclease-free Water and centrifuge for 2 min. The double-stranded cDNA will now be in the eluate (˜17.5 μl)
Proceed directly to section In Vitro Transcription to Synthesize cRNA, or place the cDNA at −20° C.
In Vitro Transcription to Synthesize cRNA:
At room temperature, prepare an IVT Master Mix by adding the following reagents to a nuclease-free microcentrifuge tube in the order listed below. Assemble enough to synthesize cRNA from all the samples in the experiment.
IVT Master Mix for a single 25 μl reaction: 2.5 μl T7 10× Reaction Buffer, 2.5 μl T7 Enzyme Mix, and 2.5 μl Biotin-NTP Mix
Mix well by gently vortexing. Centrifuge briefly (˜5 sec) to collect the IVT Master Mix at the bottom of the tube and place on ice.
Transfer 7.5 μl of IVT Master Mix to each cDNA sample (volume ˜17.5 μl). If less than 17.5 μl are eluted fill up with RNAse-free water to reach volume of 17.5 μl. Mix thoroughly by pipetting up and down 2-3 times, then flicking the tube 3-4 times, and centrifuge briefly to collect the reaction mixture in the bottom of the tube. Once assembled, place the tubes at 37° C.
Incubate reactions for 16 h. It is important to maintain a constant 37° C. incubation temperature. It is recommended to incubate in a hybridization oven because it is extremely important that condensation does not form inside the tubes; his would change the reagent concentrations and reduce yield. Alternatively you can use a thermal cycler with heated lid temperature set to 40° C.
Stop the reaction by adding 75 μl Nuclease-free Water to each cRNA sample to bring the final volume to 100 μl. Mix thoroughly by gentle vortexing. Proceed to the cRNA purification step (below) or store at −20° C.
cRNA Purification:
Preheat Nuclease-free Water to 50-60° C.
Assemble cRNA Filter Cartridges and tubes and add 350 μl of cRNA Binding Buffer to each cRNA sample. Proceed to the next step immediately.
Add 250 μl of 100% ethanol to each cRNA sample, and mix by pipetting the mixture up and down 3 times. Do NOT vortex to mix and do NOT centrifuge.
Pipet each sample mixture from step 3 onto the center of the filter in the cRNA Filter Cartridge.
Centrifuge for ˜1 min at 10,000×g. Continue until the mixture has passed through the filter.
Discard the flow-through and replace the cRNA Filter Cartridge back into the cRNA Collection Tube.
Apply 650 μl Wash Buffer to each cRNA Filter Cartridge.
Centrifuge for ˜1 min at 10,000×g, or until all the Wash Buffer is through the filter.
Discard the flow-through and spin the cRNA Filter Cartridge for an additional ˜1 min to remove trace amounts of Wash Buffer.
Transfer Filter Cartridge(s) to a fresh cRNA Collection Tube.
To the center of the filter, add 100 μl Nuclease-free Water (preheated to 50-60° C.). Leave at room temperature for 2 min and then centrifuge for ˜1.5 min at 10,000×g, or until the Nuclease-free Water is through the filter.
The cRNA will now be in the cRNA Collection Tube in ˜100 μl of Nuclease-free Water.
Quantification and Determination of Total cRNA:
The concentration of cRNA is determined by OD measurement.
The size distribution of cRNA can be checked by denaturing agarose gel electrophoresis (1% w/v) and ethidium bromide staining.
The BeadStation 500× system uses a “direct hybridization” assay, whereby gene-specific probes are used to detect labeled RNAs. Each bead in the array contains a 50-mer, sequence-specific oligo probe synthesized in-house using Illumina's Oligator™ technology. The most consistent results are achieved by hybridizing equivalent amounts of cRNA on each array. An appropriate volume of cRNA from each sample is aliquoted into the hybridization tube(s). The here described protocol is according to the manufacturer's instructions and is applicable only to 6-sample Beadchips with IntelliHyb Seal.
Preheat the oven (with rocking platform) to 58° C.
Prepare cRNA samples (dried down in a vacuum centrifuge, if necessary to achieve required concentration). To 1.5 μg cRNA, add RNase-free water up to 10 μL and mix. Leave at room temp for 10 minutes to resuspend cRNA.
Place the GEX-HYB and GEX-HCB tubes in the 58° C. oven for 10 minutes to dissolve any salts that may have precipitated in storage. Inspect the solution; if any salts remain undissolved, incubate at 58° C. for another 10 minutes. After allowing to cool to room temperature, mix thoroughly before using.
Add 20 μl GEX-HYB to each cRNA sample.
Place Illumina Hyb Chamber Gaskets into BeadChip Hyb Chamber.
Dispense 200 μl GEX-HCB into each of the two humidifying buffer reservoirs in each Hyb Chamber. Only add buffer to chambers that will be used.
Seal Hyb Chamber with lid and keep on bench at room temperature (˜22° C.) until ready to load BeadChips into Hyb Chamber.
Remove all BeadChips from their packages.
Holding BeadChip by coverseal tab with tweezers using powder-free gloved hands, slide BeadChip into Hyb Chamber Insert such that the barcode lines up with barcode symbol on the Insert.
Preheat the assay sample at 65° C. for 5 minutes.
Briefly vortex, then briefly centrifuge to collect the liquid in the bottom of the tube. Allow sample to cool to room temperature before using. Pipet sample immediately after cooling to room temp.
Load Hyb Chamber Inserts containing BeadChips into the Hyb Chamber with barcode on BeadChip aligned to barcode symbol on the Hyb Chamber.
Dispense 30 μL assay sample onto the large sample port of each array.
Seal lid onto the Hyb Chamber carefully to avoid dislodging the Hyb Chamber Insert(s).
Incubate for 16-20 h at 58° C. with rocker speed at 5.
Prepare 1× High-Temp Wash buffer (add 50 ml 10× stock to 450 ml RNAse-free water).
Place waterbath insert into heat block, and add 500 ml prepared 1× High-Temp Wash buffer.
Set heat block temp to 55° C. and pre-warm High-Temp Wash buffer to that temperature.
Close heat block lid and leave overnight.
Make Wash E1BC solution (add 7 ml E1BC buffer to 2.51 RNase-free water).
Pre-warm Block E1 buffer (4 ml/chip) to room temperature.
Prepare Block E1 buffer (2 ml/chip) with streptavidin-Cy3 (2 μL of 1 mg/ml stock per chip). Use a single conical tube for all BeadChips. Store in dark until detection step.
Remove Hyb Chamber from oven and disassemble.
Remove coverseal from the BeadChip with Beadchip submerged in ˜11 E1BC-Buffer (use glass dish for this step). Using tweezers or powder-free gloved hands, place the BeadChip into the slide rack submerged in the staining dish containing 250 ml Wash E1BC solution.
Repeat disassembly and placement in E1BC solution for all BeadChips.
Using the slide rack handle, transfer the rack into the Hybex Waterbath insert containing High-Temp Wash buffer.
Incubate static for 10 minutes with the Hybex lid closed.
During the 10-minute High-Temp Wash buffer incubation, add fresh 250 ml Wash E1BC solution to a clean staining dish.
After the 10-minute High-Temp Wash buffer incubation is complete, immediately transfer the slide rack into the staining dish containing E1BC.
Briefly agitate using rack, then shake on orbital shaker for 5 minutes at the highest speed possible without allowing solution to splash out of dish.
Transfer rack to a clean staining dish containing 250 ml 100% Ethanol (use fresh from Ethanol source bottle).
Briefly agitate using rack handle, then shake on orbital shaker for 10 minutes.
Transfer rack to a clean staining dish containing fresh 250 ml Wash E1BC solution.
Briefly agitate using rack handle, then shake on orbital shaker for 2 minutes.
Pipette 4 ml Block E1 buffer into the Wash Tray(s).
Transfer the BeadChip, face up into BeadChip Wash Tray(s) on rocker.
Rock at medium speed for 10 minutes.
Pipette 2 ml Block E1 buffer+streptavidin-Cy3 into fresh Wash Tray(s).
Transfer the BeadChip, face up into Wash Tray(s) on rocker.
Place cover on tray and rock at medium speed for 10 minutes.
Add 250 ml of Wash E1BC solution to a clean staining dish.
Transfer the BeadChip to the slide rack submerged in the staining dish.
Briefly agitate using rack, and then shake at room temp on orbital shaker for 5 minutes with Beadchips protected from light.
Prepare centrifuge with plateholders, paper towels and balance rack. Set speed to 275 rcf.
Transfer rack of BeadChips from staining dish to centrifuge and spin at room temperature for 4 min.
Store dry chips in the dark until scanned.
BeadChips are imaged using the Illumina BeadArray Reader, a two-channel, 0.8 μm resolution confocal laser scanner. The BeadArray Reader, using SentrixScan menu-driven software, automatically scans up to three different BeadChips or a SAM, hands-free, at one or at two wavelengths and creates an image file for each channel.
SEQ ID NOs:1/2gi|10863876|ref|NM—021105.1|Homo sapiens phospholipid scramblase 1 (PLSCR1), probe and coding sequence.
SEQ ID NOs:3/4gi|110611902|ref|NM—017533.2|Homo sapiens myosin, heavy chain 4, skeletal muscle (MYH4), probe and coding sequence.
SEQ ID NOs:5/6gi|90193587|ref|NM—001783.3|Homo sapiens CD79a molecule, immunoglobulin-associated alpha (CD79A), transcript variant 1, probe and coding sequence.
SEQ ID NOs:7/8gi|90193589|ref|NM—000626.2|Homo sapiens CD79b molecule, immunoglobulin-associated beta (CD79B), transcript variant 1, probe and coding sequence.
SEQ ID NOs:9/10 gi|90193589|ref|NM—000626.2|Homo sapiens CD79b molecule, immunoglobulin-associated beta (CD79B), transcript variant 1, probe and coding sequence.
SEQ ID NOs:11/12 gi|89363029|ref|NM—001039717.1|Homo sapiens chromosome 4 open reading frame 29 (C4orf29), probe and coding sequence.
SEQ ID NOs:13/14 gi|13899296|ref|NM—031458.1|Homo sapiens poly (ADP-ribose) polymerase family, member 9 (PARP9), probe and coding sequence.
SEQ ID NOs:15/16 gi|166091436|ref|NM—001716.3|Homo sapiens chemokine (C—X—C motif) receptor 5 (CXCR5), transcript variant 1, probe and coding sequence.
SEQ ID NOs:17/18 gi|50428916|ref|NM—001002264.1|Homo sapiens epithelial stromal interaction 1 (breast) (EPSTI1), transcript variant 1, probe and coding sequence.
SEQ ID NOs:19/20 gi|118402587|ref|NM—002120.3|Homo sapiens major histocompatibility complex, class II, DO beta (HLA-DOB), probe and coding sequence.
SEQ ID NOs:21/22 gi|59853527|ref|NM—004737.3|Homo sapiens like-glycosyltransferase (LARGE), transcript variant 1, probe and coding sequence.
SEQ ID NOs:23/24 gi|20149601|ref|NM—012229.2|Homo sapiens 5′-nucleotidase, cytosolic II (NT5C2), probe and coding sequence.
SEQ ID NOs:25/26 gi|166706910|ref|NM—006417.4|Homo sapiens interferon-induced protein 44 (IFI44), probe and coding sequence.
SEQ ID NOs:27/28 gi|154091031|ref|NM—144590.2|Homo sapiens ankyrin repeat domain 22 (ANKRD22), probe and coding sequence.
SEQ ID NOs:29/30 gi|22027643|ref|NM—002257.2|Homo sapiens kallikrein 1 (KLK1), probe and coding sequence.
SEQ ID NOs:31/32 gi|22202620|ref|NM—000846.3|Homo sapiens glutathione S-transferase A2 (GSTA2), probe and coding sequence.
SEQ ID NOs:33/34 gi|22748768|ref|NM—152355.1|Homo sapiens zinc finger protein 441 (ZNF441), probe and coding sequence.
SEQ ID NOs:35/36 gi|122937216|ref|NM—001080411.1|Homo sapiens zinc finger protein 433 (ZNF433), probe and coding sequence.
SEQ ID NOs:37/38 gi|68348721|ref|NM—021950.3|Homo sapiens membrane-spanning 4-domains, subfamily A, member 1 (MS4A1), transcript variant 3, probe and coding sequence.
SEQ ID NOs:39/40 gi|23111059|ref|NM—005850.3|Homo sapiens splicing factor 3b, subunit 4, 49 kDa (SF3B4), probe and coding sequence.
SEQ ID NOs:41/42 gi|24308268|ref|NM—021218.1|Homo sapiens chromosome 9 open reading frame 80 (C9orf80), probe and coding sequence.
SEQ ID NOs:43/44 gi|53759115|ref|NM—000593.5|Homo sapiens transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) (TAP1), probe and coding sequence.
SEQ ID NOs:45/46 gi|26787992|ref|NM—006873.2|Homo sapiens stonin 1 (STON1), probe and coding sequence.
SEQ ID NOs:47/48 gi|78190479|ref|NM—001034837.1|Homo sapiens Kv channel interacting protein 1 (KCNIP1), transcript variant 1, probe and coding sequence.
SEQ ID NOs:49/50 gi|27894318|ref|NM—173842.1|Homo sapiens interleukin 1 receptor antagonist (IL1RN), transcript variant 1, probe and coding sequence.
SEQ ID NOs:51/52 gi|28302128|ref|NM—000518.4|Homo sapiens hemoglobin, beta (HBB), probe and coding sequence.
SEQ ID NOs:53/54 gi|117606369|ref|NM—207315.2|Homo sapiens cytidine monophosphate (UMP-CMP) kinase 2, mitochondrial (CMPK2), nuclear gene encoding mitochondrial protein, probe and coding sequence.
SEQ ID NOs:55/56 gi|50263054|ref|NM—178483.2|Homo sapiens chromosome 20 open reading frame 79 (C20orf79), probe and coding sequence.
SEQ ID NOs:57/58 gi|93102363|ref|NM—015055.2|Homo sapiens SWAP-70 protein (SWAP70), probe and coding sequence.
SEQ ID NOs:59/60 gi|144953890|ref|NM—017935.3|Homo sapiens B-cell scaffold protein with ankyrin repeats 1 (BANK1), transcript variant 1, probe and coding sequence.
SEQ ID NOs:61/62 gi|33598961|ref|NM—004443.3|Homo sapiens EPH receptor B3 (EPHB3), probe and coding sequence.
SEQ ID NOs:63/64 gi|33859792|ref|NM—173494.1|Homo sapiens chromosome X open reading frame 41 (CXorf41), probe and coding sequence.
SEQ ID NOs:65/66 gi|34147320|ref|NM—005533.2|Homo sapiens interferon-induced protein 35 (IFI35), probe and coding sequence.
SEQ ID NOs:67/68 gi|34147598|ref|NM—002002.3|Homo sapiens Fc fragment of IgE, low affinity II, receptor for (CD23) (FCER2), probe and coding sequence.
SEQ ID NOs:69/70 gi|34147611|ref|NM—024670.3|Homo sapiens suppressor of variegation 3-9 homolog 2 (Drosophila) (SUV39H2), probe and coding sequence.
SEQ ID NOs:71/72 gi|34147626|ref|NM—023926.3|Homo sapiens zinc finger and SCAN domain containing 18 (ZSCAN18), probe and coding sequence.
SEQ ID NOs:73/74 gi|153070786|ref|NR—003608.1|Homo sapiens tubulin, alpha pseudogene (MGC16703) on chromosome, probe and coding sequence.
SEQ ID NOs:75/76 gi|153252109|ref|NM—145051.3|Homo sapiens ring finger protein 183 (RNF183), probe and coding sequence.
SEQ ID NOs:77/78 gi|46370097|ref|NM—024026.4|Homo sapiens mitochondrial ribosomal protein 63 (MRP63), nuclear gene encoding mitochondrial protein, probe and coding sequence.
SEQ ID NOs:79/80 gi|76781490|ref|NM—007047.3|Homo sapiens butyrophilin, subfamily 3, member A2 (BTN3A2), probe and coding sequence.
SEQ ID NOs:81/82 gi|44771200|ref|NM—030628.1|Homo sapiens integrator complex subunit 5 (INTS5), probe and coding sequence.
SEQ ID NOs:83/84 gi|38016929|ref|NM—198213.1|Homo sapiens 2′-5′-oligoadenylate synthetase-like (OASL), transcript variant 2, probe and coding sequence.
SEQ ID NOs:85/86 gi|38157980|ref|NM—004223.3|Homo sapiens ubiquitin-conjugating enzyme E2L 6 (UBE2L6), transcript variant 1, probe and coding sequence.
SEQ ID NOs:87/88 gi|38195085|ref|NM—022098.2|Homo sapiens X-prolyl aminopeptidase (aminopeptidase P) 3, putative (XPNPEP3), probe and coding sequence.
SEQ ID NOs:89/90 gi|109633030|ref|NM—198253.2|Homo sapiens telomerase reverse transcriptase (TERT), transcript variant 1, probe and coding sequence.
SEQ ID NOs:91/92 gi|150010588|ref|NM—003641.3|Homo sapiens interferon induced transmembrane protein 1 (9-27) (IFITM1), probe and coding sequence.
SEQ ID NOs:93/94 gi|40254458|ref|NM—001884.2|Homo sapiens hyaluronan and proteoglycan link protein 1 (HAPLN1), probe and coding sequence.
SEQ ID NOs:95/96 gi|142357995|ref|NM—144682.4|Homo sapiens schlafen family member 13 (SLFN13), probe and coding sequence.
SEQ ID NOs:97/98 gi|154350243|ref|NM—001100411.1|Homo sapiens chromosome 6 open reading frame 60 (C6orf60), transcript variant 2, probe and coding sequence.
SEQ ID NOs:99/100 gi|40288190|ref|NM—017523.2|Homo sapiens XIAP associated factor 1 (XAF1), transcript variant 1, probe and coding sequence.
SEQ ID NOs:101/102 gi|40807470|ref|NM—003594.3|Homo sapiens transcription termination factor, RNA polymerase II (TTF2), probe and coding sequence.
SEQ ID NOs:103/104 gi|41281452|ref|NM—014720.2|Homo sapiens STE20-like kinase (yeast) (SLK), probe and coding sequence.
SEQ ID NOs:105/106 gi|41393588|ref|NM—024769.2|Homo sapiens adipocyte-specific adhesion molecule (ASAM), probe and coding sequence.
SEQ ID NOs:107/108 gi|156523233|ref|NM—001721.6|Homo sapiens BMX non-receptor tyrosine kinase (BMX), transcript variant 2, probe and coding sequence.
SEQ ID NOs:109/110 gi|157168354|ref|NM—001771.2|Homo sapiens CD22 molecule (CD22), probe and coding sequence.
SEQ ID NOs:111/112 gi|91807109|ref|NM—001040031.1|Homo sapiens CD37 molecule (CD37), transcript variant 2, probe and coding sequence.
SEQ ID NOs:113/114 gi|166706902|ref|NM—002053.2|Homo sapiens guanylate binding protein 1, interferon-inducible, 67 kDa (GBP1), probe and coding sequence.
SEQ ID NOs:115/116 gi|53759142|ref|NM—002061.2|Homo sapiens glutamate-cysteine ligase, modifier subunit (GCLM), probe and coding sequence.
SEQ ID NOs:117/118 gi|61888835|ref|NM—003121.2|Homo sapiens Spi-B transcription factor (Spi-1/PU.1 related) (SPIB), probe and coding sequence.
SEQ ID NOs:119/120 gi|45243546|ref|NM—203488.1|Homo sapiens acylphosphatase 1, erythrocyte (common) type (ACYP1), transcript variant 2, probe and coding sequence.
SEQ ID NOs:121/122 gi|62912451|ref|NM—016824.3|Homo sapiens adducin 3 (gamma) (ADD3), transcript variant 1, probe and coding sequence.
SEQ ID NOs:123/124 gi|47157326|ref|NM—005400.2|Homo sapiens protein kinase C, epsilon (PRKCE), probe and coding sequence.
SEQ ID NOs:125/126 gi|5453622|ref|NM—006314.1|Homo sapiens connector enhancer of kinase suppressor of Ras 1 (CNKSR1), probe and coding sequence.
SEQ ID NOs:127/128 gi|156713456|ref|NM—006542.3|Homo sapiens S-phase response (cyclin-related) (SPHAR), probe and coding sequence.
SEQ ID NOs:129/130 gi|112293284|ref|NM—006717.2|Homo sapiens spindlin 1 (SPIN1), probe and coding sequence.
SEQ ID NOs:131/132 gi|166706908|ref|NM—006820.2|Homo sapiens interferon-induced protein 44-like (IFI44L), probe and coding sequence.
SEQ ID NOs:133/134 gi|150378462|ref|NM—001099412.1|Homo sapiens MYST histone acetyltransferase (monocytic leukemia) 3 (MYST3), transcript variant 1, probe and coding sequence.
SEQ ID NOs:135/136 gi|62865863|ref|NM—000519.3|Homo sapiens hemoglobin, delta (HBD), probe and coding sequence.
SEQ ID NOs:137/138 gi|62865863|ref|NM—000519.3|Homo sapiens hemoglobin, delta (HBD), probe and coding sequence.
SEQ ID NOs:139/140 gi|154426252|ref|NM—001100422.1|Homo sapiens viral DNA polymerase-transactivated protein 6 (LOC26010), transcript variant 2, probe and coding sequence.
SEQ ID NOs:141/142 gi|50593017|ref|NM—016371.2|Homo sapiens hydroxysteroid (17-beta) dehydrogenase 7 (HSD17B7), probe and coding sequence.
SEQ ID NOs:143/144 gi|75750528|ref|NM—016552.2|Homo sapiens ankyrin repeat and MYND domain containing 1 (ANKMY1), transcript variant 1, probe and coding sequence.
SEQ ID NOs:145/146 gi|51593093|ref|NM—017946.2|Homo sapiens FK506 binding protein 14, 22 kDa (FKBP14), probe and coding sequence.
SEQ ID NOs:147/148 gi|169160852|refIXR—037068.1|PREDICTED: Homo sapiens misc_RNA (LOC646970), probe and coding sequence.
| Number | Date | Country | Kind |
|---|---|---|---|
| 08160649.3 | Jul 2008 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2009/059065 | 7/15/2009 | WO | 00 | 4/4/2011 |
