OBJECTIVE To demonstrate the ability of the nCounter Analysis System, a nanowire technology, to sensitively and accurately detect cancer-testis antigens (CTAs) in men with prostate cancer and correlate them with disease parameters. The clinical implementation of novel biomarkers is necessary to provide for individual disease treatment planning for men with prostate cancer. The CTAs, as cancer-associated biomarkers that may correlate with aggressive disease, have the potential to play an important role. METHODS Formalin-fixed, paraffin embedded samples were used from men undergoing radical prostatectomy for prostate cancer. The expression of CTAs along with control genes was measured from formalin-fixed, paraffin-embedded prostate cancer tissues using real-time polymerase chain reaction and the nCounter assay. RESULTS Using a nanowire-based assay, ribonucleic acid (RNA) expression levels of the CTAs CSAG2 and NOL4 were found to be significantly higher in men with Gleason score (GS) 8-10 disease than those with GS <= 4+3 disease. On the contrary, the RNA expression level of PAGE4 was lower in men with GS 8-10 disease than those with GS <= 6 group. This study demonstrates that CTAs can be detected with a nanostring assay that is translatable and that a set of CTAs correlates with the clinical characteristics of the disease. CONCLUSION CTAs represent unique, cancer-associated biomarkers with potential utility in the clinic. The nCounter nanowire technology provides an opportunity to evaluate this panel of CTAs associated with aggressive prostate cancer in a multi-institutional fashion. (C) 2015 Elsevier Inc.
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Mashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Mashhad Univ Med Sci, Basic Sci Res Inst, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Mahmoudian, Reihaneh Alsadat
Amirhosein, Maharati
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Mashhad Univ Med Sci, Student Res Comm, Fac Med, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Amirhosein, Maharati
Mahmoudian, Parvaneh
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Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
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Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad, Iran
Mashhad Univ Med Sci, Metab Syndrome Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Maftooh, Mina
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Khazaei, Majid
Nassiri, Mohammadreza
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Ferdowsi Univ Mashhad, Res Inst Biotechnol, Recombinant Prot Res Grp, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Nassiri, Mohammadreza
Hassanian, Seyed Mahdi
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Mashhad Univ Med Sci, Basic Sci Res Inst, Mashhad, Iran
Mashhad Univ Med Sci, Metab Syndrome Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Hassanian, Seyed Mahdi
Ghayour-Mobarhan, Majid
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Mashhad Univ Med Sci, Basic Sci Res Inst, Mashhad, Iran
Mashhad Univ Med Sci, Metab Syndrome Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Ghayour-Mobarhan, Majid
Ferns, Gordon
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Brighton & Sussex Med Sch, Dept Med Educ, Brighton BN1 9PH, Sussex, EnglandMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Ferns, Gordon
Shahidsales, Soodabeh
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Mashhad Univ Med Sci, Canc Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
Shahidsales, Soodabeh
Avan, Amir
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Mashhad Univ Med Sci, Basic Sci Res Inst, Mashhad, Iran
Mashhad Univ Med Sci, Med Genet Res Ctr, Mashhad, Iran
Mashhad Univ Med Sci, Metab Syndrome Res Ctr, Mashhad, IranMashhad Univ Med Sci, Canc Res Ctr, Mashhad, Iran
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Shahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, IranShahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, Iran
Seifi-Alan, Mahnaz
Shamsi, Roshanak
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Shahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, IranShahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, Iran
Shamsi, Roshanak
Esfandiary, Ali
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Shahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, IranShahid Beheshti Univ Med Sci, Dept Med Genet, POB 1985717443, Tehran, Iran