RNA blood levels of osteopontin splice variants are cancer markers
© Hartung and Weber; licensee Springer. 2013
Received: 22 January 2013
Accepted: 5 March 2013
Published: 14 March 2013
Despite a sizeable and continuously growing literature on osteopontin and cancer the molecule has not yet found entry into clinical diagnostics. Our identification of spliced variants that are more specific for cancer than the full-length transcript has opened new possibilities for reaching this goal.
Here we have developed a real-time RT-PCR blood test and evaluated it in a pilot study of breast, lung, pancreatic, gynecologic, and other cancers, compared to non-cancer controls.
Osteopontin-b was increased in lung cancers and pancreatic cancers. When applying a cutoff of 2 standard deviations above normal, elevation in osteopontin-b transcripts detected over 40% of lung cancers. Osteopontin-c was increased in gynecologic and pancreatic cancers. Elevation in osteopontin-c of 2 standard deviations above the normal mean value also detected a fraction of breast cancers and lung cancers, suggesting heterogeneity within those types of tumors. Specifically, breast carcinomas were associated with significantly higher levels of osteopontin-c mRNA in the blood than carcinomas in situ. In lung cancer patients, the osteopontin-c blood RNA levels had an increasing trend with tumor grade.
Osteopontin-b and -c in the blood are biomarkers for distinct cancers. Our investigations may have bearing on cancer screening and diagnosis.
Reliable blood tests for early detection and monitoring of progression are a holy grail in cancer diagnostics. They require the sufficiently abundant presence of a molecule that is uniquely associated with the presence or the progression of a particular type of cancer or multiple cancers. While a plethora of biomarkers has been described in the literature, few have achieved routine clinical use. Among them, PSA for the early detection as well as treatment monitoring of prostate cancer stands out. CEA is elevated in the blood of patients with colorectal, gastric, pancreatic, lung or breast carcinomas. CEA is mainly used to identify recurrence after surgical resection, because the blood test is not reliable as a screening test for early detection. CA125 is a marker for ovarian or endometrial cancers. However, it can also be elevated by uterine fibroids, endometriosis, pelvic inflammatory disease and cirrhosis, as well as in pregnancy and during menstruation.
While biomarkers for specific types of cancer have value, markers that detect multiple cancers may be more beneficial in diagnostic screening, where it is impractical to have one marker for every possible cancer. As such, gene products of cancer progression often are generated as splice variants that are absent from untransformed tissues. Because the same mechanisms for progression are used by various cancers these molecules may broadly indicate the presence of a cancer in the patient.
Osteopontin has been associated with the progression of numerous types of cancer (Weber et al. 2010; Weber et al. 2011; Weber 2011). Although the molecule has been studied as a marker for malignancy over more than 20 years (Craig et al. 1988; Senger et al. 1989) it has not yet found clinical use as a diagnostic. The full-length form of osteopontin (osteopontin-a) acts as a TH1 cytokine that may be secreted by macrophages and T-lymphocytes and is elevated in the blood during immune responses, limiting its value as a cancer marker. We have identified the splice variant osteopontin-c (He et al. 2006) to be selectively present in multiple cancers (Sullivan et al. 2009; Tilli et al. 2011) and to serve as a marker for tumor grade (Mirza et al. 2008). These studies were done by immunohistochemistry or real-time RT-PCR on the cancer tissues. The value of the biomarker may be increased if it can be identified in patient blood and can be correlated to clinical determinants of cancer. Because we had previously developed a real-time RT-PCR protocol to quantify the RNA messages of all three osteopontin splice variants in breast cancer specimens, we adapted it to the analysis of total RNA extracted from whole blood. We tested the hypothesis that aggressive cancers continuously shed cells into the circulation, which are detectable by their unique production of spliced osteopontin mRNA.
Materials and methods
Patient samples were obtained under IRB (Institutional Review Board) protocols 04-01-29-01 and 09-11-09-03 (University of Cincinnati). There were several sources of patient blood. Whole blood was collected from breast cancer patients after obtaining informed consent. The blood was frozen immediately on dry ice. Some blood samples (including pancreatic and gynecologic cancers) were also obtained from CHTN (Collaborative Human Tissue Network). Pelleted nucleated cells from lung cancer patients were provided by the University of Cincinnati tissue procurement service. Blood RNA from breast cancer patients and normal controls was obtained from the Division of Human Genetics at The Ohio State University. Other cancers entailed 1 hepatocellular carcinoma and 2 colorectal adenocarcinomas.
RNA was extracted from whole blood with RNazol RT (Molecular Research Center Inc.). The extraction of RNA from nucleated cells was accomplished with TriReagent-RT Blood (Molecular Research Center Inc.). No RNA extraction was required for the Ohio State University samples, as they were provided as RNA samples.
All PCR reactions were performed on an ABI Prism 7000 cycler using SYBR Green detection format. cDNA was made from 1 μg RNA in a 20 μl reaction using the iScript reverse transcription kit (BioRad). 5 μl (for actin 2.5 μl) cDNA was added to each PCR reaction in a total volume of 25 μl using the standard PCR buffer system with optimized concentrations of MgCl2. For each experiment a no-template reaction was included as a negative control. cDNA from MDA-MB-435 cells, which express endogenous osteopontin splice variants, served as a reference in every run. The primer combinations were described previously (Mirza et al. 2008). The conditions for PCR were 94°C denaturation for 120 s followed by 40 cycles of: 94°C melting for 15 s, 58°C annealing for 30 s, extension at 72°C for 30 s, followed by 72°C for 2 min and 4°C for 5 min, and a melting curve program (the amplification efficiency was only minimally affected by using the same annealing temperature for all PCR reactions, compared to Mirza et al. (2008) which had optimized the annealing temperatures individually; the amplification efficiency is accounted for in the calculations of relative RNA abundance). Product purity, product size, and absence of primer dimers were confirmed by DNA melting curve analysis and agarose gel electrophoresis. Melt curves yielded a single sharp peak for all template reactions, and a minimal melt peak (resulting from primer dimers) or no melt peaks for the no-template control reactions (Mirza et al. 2008). Relative expression ratios of the target genes were calculated from the cycle threshold and efficiency measurements (Pfaffl 2001).
To assess the sensitivity of the assay, we titrated MDA-MB-435 cells, which express all three forms of osteopontin (He et al. 2006) and served here as the reference cell line, into normal blood. RNA was then extracted for real-time RT-PCR. The relative abundance was calculated according to the method of Pfaffl (2001) using the average of all undiluted MDA-MB-435 real-time RT-PCR results (the positive control and reference in all blood RT-PCR runs) as the reference value.
Each data set was analyzed for equality of variances using the Levene test. The Kolmogorov-Smirnov test was applied to determine which of the data sets had a normal distribution. Since none of the datasets followed a normal distribution, they were analyzed with the Kruskal-Wallis Test. A significant value (p<.05) signifies that the medians of the groups being tested are not equal. The non-parametric test uses medians to test the groups rather than the means because medians are robust estimators that are resistant to outliers. In the cases with the significant results (except for single pairwise results), a non-parametric procedure was performed in SAS, PROC MULTTEST, to analyze the differences between the cancer groups and the control by setting up individual contrasts. This is analogous to independent t-tests, in which one controls for the type I error rate using a method such as bootstrapping. The bootstrap method is a non-parametric approach involving multiple re-sampling of the data. Using this SAS procedure, a reproduction of the Dunnett’s test was set up to determine the relationship between osteopontin splice variant levels and clinical variables (tumor stage, tumor grade, primary tumor size), Spearman’s correlation coefficient and its associated p-value were calculated.
We asked whether there are differences among the histologic subtypes of lung cancer with regard to the abundance of osteopontin splice variant RNA in the blood. There were no differences for osteopontin-a, osteopontin-b or osteopontin-c among adenocarcinoma (n = 26), non-small cell lung cancer (n = 4), and squamous cell carcinoma (n = 11) according to the Kruskal-Wallis test (four lung cancers were diagnosed as carcinoid tumor, small cell cancer, pleomorphic carcinoma, non-mucinous bronchioloalveolar carcinoma, and were not included in this analysis). Similarly, there were no differences in abundance of the splice variants between ductal (n = 58) and lobular (n = 7) breast cancers (two cancers were mucinous carcinomas).
Cancer stage and primary tumor size
A. lung cancer
lung cancer stage
lung cancer size
B. breast cancer
breast cancer stage T
breast cancer stage N
breast cancer size
Information on conventional biomarkers was available for several tumors. In the lung cancers, there was no difference in osteopontin-a, osteopontin-b or osteopontin-c between the TFF1+ (n = 12) and the TFF1- (n = 10) subgroups or between the P63+ (n = 8) and P63- (n = 5) subgroups. There were also no differences in osteopontin splice variant levels between CK-7+ (n = 12) and CK-7- (n = 3) lung cancers or between CK-5/6+ (n = 2) and CK-5/6- (n = 5) lung cancers. ER, PR, and HER2 are standard biomarkers for breast cancer that determine treatment decisions. Again, osteopontin-a displayed a wide scatter with outlier samples in the marker-positive and marker-negative groups. In this analysis, osteopontin-c also had one outlier with a high value in the ER- PR- breast cancer group and no significant differences between the groups (not shown). The only significant difference detected was for osteopontin-b between ER- (mean value 0.0098, n = 13) and ER+ (mean value 0.004, n = 49) breast cancers, the relevance of which remains to be elucidated as osteopontin-b was not found to be elevated in breast cancers over control specimens.
Here we describe the real-time RT-PCR detection of osteopontin splice variants in whole blood. While osteopontin-b is a marker for lung cancers and pancreatic cancers. osteopontin-c is increased in gynecologic and pancreatic cancers. However, osteopontin-c also detects fractions of breast cancers and of lung cancers, suggesting heterogeneity within those types of tumors.
Possibly the most striking and unexpected finding of this study was the elevation of osteopontin-b in the blood of a large fraction of lung cancer patients (over 55% elevated more than one standard deviation above the healthy mean value). Osteopontin-b RNA in the blood is a biomarker for lung cancers. Although osteopontin-c was not identified as a marker when considering all lung cancers together, close to 40% of patients had elevated levels of at least one standard deviation above the healthy mean value, and there was a trend toward higher osteopontin-c levels in higher grade cancers. By ELISA (which does not distinguish among splice variants), elevated circulating levels of osteopontin protein have been found to be associated with lung cancer (Chang et al. 2007; Mountzios et al. 2007; Fedarko et al. 2001) and to be predictors of prognosis (Mack et al. 2008). Of note, the osteopontin protein levels in the blood are likely mostly generated by the primary cancer or its established metastases, whereas the blood RNA levels are thought to come entirely from circulating tumor cells.
In breast cancer tissue, osteopontin-c (measured by real-time RT-PCR or immunohistochemistry) is present in over 75% of cases and serves as a marker of tumor grade (Mirza et al. 2008). Unexpectedly, the blood real-time RT-PCR measurements of this study did not find the same correlations. Only about 30% of breast cancers generated blood levels of osteopontin-c that exceeded one standard deviation above the mean value of healthy controls. Clearly, breast cancers were associated with higher osteopontin-c blood RNA levels than in situ carcinomas. Osteopontin-c showed no association with ER, PR, or HER2. While this is in line with its previously reported association with triple negative breast cancer (Mirza et al. 2008; Weber 2011; Weber et al. 2011), there were only five triple negative breast cancers in this study - too few to confirm any association with this subset. Further investigations are required to elucidate the subfractions of breast cancers that cause elevated blood mRNA for osteopontin-c. We have previously found osteopontin-b in breast tissue not to be a marker for breast cancer (Mirza et al. 2008). Consistently, the mean value of osteopontin-b in all breast cancers is not elevated over the mean value in healthy controls, and osteopontin-b does not increase in cancer over in situ carcinomas. Therefore, the difference in osteopontin-b levels between ER+ and ER- breast cancers is surprising. As neither subgroup has significantly higher osteopontin-b values than healthy controls, the difference is not of diagnostic value for cancer.
Our protocol was intended to provide a sensitive screening test that may detect the presence of cancer (without selectivity for a particular type of cancer). While the approach has high specificity, with the available technology it has limited sensitivity. Rather than standing alone as diagnostics in screening, osteopontin splice mRNA blood levels may find use in monitoring cancer progression or in multi-marker panels (see Weber 2011).
A flexible threshold (set as the inversion point on the logarithmic plot of the amplification curves) did not improve the readings over a fixed threshold. A conventional comparative threshold method is similar to the one used here, but neglects to account for differences in amplification efficiencies by setting E = 2.
Osteopontin-b and -c in the blood are biomarkers for distinct cancers. Osteopontin-b is increased in lung cancer patients and pancreatic cancer patients. Osteopontin-c is increased in gynecologic and pancreatic cancers, as well as a fraction of breast cancers and lung cancers. Specifically, breast carcinomas are associated with significantly higher levels of osteopontin-c mRNA in the blood than carcinomas in situ. In lung cancer patients, the osteopontin-c blood RNA levels have an increasing trend with tumor grade. Our investigations may have bearing on cancer screening and diagnosis.
This research was supported by DOD grants BC095225 and PR094070 to GFW. Biomathematics support was provided by Michael O’Brien. Dr. Beth Shaughnessy generously provided the University of Cincinnati whole blood samples. The University of Cincinnati Cancer Institute Tumor Bank (UCCITB) generously supplied the pelleted nuclear cells.
- Beitsch PD, Clifford E: Detection of carcinoma cells in the blood of breast cancer patients. Am J Surgery 2000, 180: 446-449. 10.1016/S0002-9610(00)00518-3View ArticleGoogle Scholar
- Chang YS, Kim HJ, Chang J, Ahn CM, Kim SK, Kim SK: Elevated circulating level of osteopontin is associated with advanced disease state of non-small cell lung cancer. Lung Cancer 2007, 57: 373-380. 10.1016/j.lungcan.2007.04.005View ArticleGoogle Scholar
- Craig AM, Nemir M, Mukherjee BB, Chambers AF, Denhardt DT: Identification of the major phosphoprotein secreted by many rodent cell lines as 2ar/osteopontin: enhanced expression in H-ras-transformed 3 T3 cells. Biochem Biophys Res Commun 1988, 157: 166-173. 10.1016/S0006-291X(88)80028-7View ArticleGoogle Scholar
- Fedarko NS, Jain A, Karadag A, Van Eman MR, Fisher LW: Elevated serum bone sialoprotein and osteopontin in colon, breast, prostate, and lung cancer. Clin Cancer Res 2001, 7: 4060-4066.Google Scholar
- Hardingham JE, Hewett PJ, Sage RE, Finch JL, Nuttall JD, Kotasek D, Dobrovic A: Molecular detection of blood-borne epithelial cells in colorectal cancer patients and in patients with benign bowel disease. Int J Cancer 2000, 89: 8-13. 10.1002/(SICI)1097-0215(20000120)89:1<8::AID-IJC2>3.0.CO;2-KView ArticleGoogle Scholar
- He B, Mirza M, Weber GF: An osteopontin splice variant induces anchorage independence in human breast cancer. Oncogene 2006, 25: 2192-2202. 10.1038/sj.onc.1209248View ArticleGoogle Scholar
- Mack PC, Redman MW, Chansky K, Williamson SK, Farneth NC, Lara PN Jr, Franklin WA, Le QT, Crowley JJ, Gandara DR, SWOG: Lower osteopontin plasma levels are associated with superior outcomes in advanced non-small-cell lung cancer patients receiving platinum-based chemotherapy: SWOG Study S0003. J Clin Oncol 2008, 26: 4771-4776. 10.1200/JCO.2008.17.0662View ArticleGoogle Scholar
- Mirza M, Shaughnessy E, Hurley JK, Vanpatten KA, Pestano GA, He B, Weber GF: Osteopontin-c is a selective marker for breast cancer. Int J Cancer 2008, 122: 889-897. 10.1002/ijc.23204View ArticleGoogle Scholar
- Mountzios G, Dimopoulos MA, Bamias A, Papadopoulos G, Kastritis E, Syrigos K, Pavlakis G, Terpos E: Abnormal bone remodeling process is due to an imbalance in the receptor activator of nuclear factor-kappaB ligand (RANKL)/osteoprotegerin (OPG) axis in patients with solid tumors metastatic to the skeleton. Acta Oncol 2007, 46: 221-229. 10.1080/02841860600635870View ArticleGoogle Scholar
- Pfaffl MW: A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 2001, 29: e45. 10.1093/nar/29.9.e45View ArticleGoogle Scholar
- Senger DR, Perruzzi CA, Papadopoulos A: Elevated expression of secreted phosphoprotein I (osteopontin, 2ar) as a consequence of neoplastic transformation. Anticancer Res 1989, 9: 1291-1299.Google Scholar
- Sullivan J, Blair L, Alnajar A, Aziz T, Ng CY, Chipitsyna G, Gong Q, Witkiewicz W, Weber GF, Yeo CJ, Arafat HA: Expression of a pro-metastatic splice variant of Osteopontin, OPNc, in human pancreatic ductal adenocarcinoma. Surgery 2009, 146: 232-240. 10.1016/j.surg.2009.03.036View ArticleGoogle Scholar
- Tilli TM, Franco VF, Robbs BK, Wanderley JL, Silva F, Duarte de Mello K, Viola JPB, Weber GF, Gimba ERP: Osteopontin-c splicing isoform contributes to ovarian cancer progression. Mol Cancer Res 2011, 9: 280-293. 10.1158/1541-7786.MCR-10-0463View ArticleGoogle Scholar
- Weber GF, Lett S, Haubein N: Osteopontin is a marker for cancer aggressiveness and patient survival. Brit J Cancer 2010, 103: 861-869. 10.1038/sj.bjc.6605834View ArticleGoogle Scholar
- Weber GF, Lett GS, Haubein NC: Meta-analysis of Osteopontin as a clinical cancer marker. Oncol Rep 2011, 25: 433-441.View ArticleGoogle Scholar
- Weber GF: The cancer biomarker osteopontin: combination with other markers. Cancer Genomics Proteomics 2011, 8: 263-288.Google Scholar
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