miR-203 is a predictive biomarker for colorectal cancer and its expression is associated with BIRC5

Tumor Biology - Tập 37 - Trang 15989-15995 - 2016
Qiang Fu1, Jun Zhang1, Xin Xu1, Fei Qian1, Ke Feng1, Jie Ma2
1Department of General Surgery, The Sixth Affiliated Hospital of Kunming Medical University, Yuxi, China
2Department of Pathology, Zhejiang Provincial People’s Hospital, Hangzhou, China

Tóm tắt

The purpose of this study was to explore the role of miR-203 in colorectal cancer (CRC) and evaluate the correlation between miR-203 and BIRC5. The expressions of miR-203 in the tissues of 122 CRC patients (with non-tumor tissues as controls) and those from 30 healthy donors were detected by TaqMan® MicroRNA assay. BIRC5s expressions in CRC and non-tumor tissues were detected by immunohistochemistry. Significantly less miR-203 was expressed in CRC tissues (P < 0.05) than in non-tumor tissues. Furthermore, low expression level of miR-203 was correlated with distant metastasis (DM), lymph node metastasis (LNM), and TNM stage (P < 0.05), but there were no significant differences between tumor size or gender. The positive expression rates of BIRC5 in CRC and non-tumor tissues were 73.77 % (90/122) and 30.32 % (37/122), respectively. The expression intensity of BIRC5 in CRC was significantly higher than that of non-tumor tissues (P < 0.05). It was significantly correlated with DM, LNM, and TNM stage (P < 0.05). Finally, miR-203 expression was negatively associated with that of BIRC5 (r = −0.8150, P < 0.05). In conclusion, miR-203 was down-regulated in CRC tissues and involved in the onset and progression of CRC. The expressions of miR-203 and BIRC5 in CRC were significantly negatively correlated, suggesting that BIRC5 may be regulated by miR-203. miR-203 is a potential suppressor and predictive biomarker for CRC.

Tài liệu tham khảo

Siegel R, Desantis C, Jemal A. Colorectal cancer statistics. CA Cancer J Clin. 2014;64(2):104–17. Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90. Tao K, Yang J, Guo Z, Hu Y, Sheng H, Gao H, Yu H, et al. Prognostic value of miR-221-3p, miR-342-3p and miR-491-5p expression in colon cancer. Am J Transl Res. 2014;6(4):391–401. AG X, ZJ Y, Jiang B, Wang XY, Zhong XH, Liu JH, Lou QY, Gan AH. Coloerectal cancer in Guangdong Province of China: a demographic and anatomic survey. World J Gastroenterol. 2010;16:906–65. Weitz J, Koch M, Debus J, Hohler T, Galle PR, et al. Colorectal cancer. Lancet. 2005;365:153–65. Kozomara A, Griffths-Jones S. miRBase: annotationg high confidence microRNAs using deep sequencing data. Nucleic Acids Res. 2014;42:68–73. Earle JS, Luthra R, Romans A, et al. Association of microRNA expression with microsatellite instability status in colorectal adeno carcinoma[J. Mol Diagn. 2010;12:433–40. Chen DL, Wang ZQ, Zl Z. Identificantion of miR 214 as a negative regulator of colorectal cancer liver metastasis via regulation of FGFR 1 expression. Hepatology. 2014;60(2):598–609. Zhang H, Li W, Nan F, Wang H, Xu Y, et al. MicroRNA expression profile of colon cancer stem-like cells in HT 29 adenocarcinoma cell line. Biochem Biophys Res Commun. 2011;404:273–8. Iorio MV, Croce CM. MicroRNA dysregulation in cancer: diagnostics, monitoring, and therapeutics. A comprehensive review. EMBO Mol Med. 2012. doi:10.1002/emmm.201100209. Pavlyukov MS, Antipova NV, Balashova MV, et al. Survivin monomer plays an essential role in apoptosis regulation. J Biol Chem. 2011;286:23296–307. Lamers F, Schild L, Koser J, et al. Targeted BIRC5 silencing using YM155 causes cell death in neuroblastoma cells with low ABCB1 expression. Eur J Cancer. 2012;5:763–71. Tao H-Q, He X-J, Ma Y-Y, et al. Evaluation of REG4 for early diagnosis and prognosis of gastric cancer. Hum Pathol. 2011;42:1401–9. Hussain MU. Micro-RNAs (miRNAs): genomic organization, biogenesis and mode of action. Cell Tissue Res. 2012;349(2):405–13. Smith CM, Watson DI, Michael MZ, Hussey DJ. MicroRNAs development of Barrett’s esophagus, and progression to esophageal adenocarcinoma. World J of Gastroenterology 2010;6:531–537. Furuta M, Kozaki K-i, Tanaka S, et al. miR-124 and miR-203 are epigenetically silenced tumor-suppressive microRNAs in hepatocellular carcinoma. Carcinogenesis. 2010;31(5):766–76. Viticchie G, Lena AM, Latina A, Formosa A, Gregersen LH, et al. miR-203 controls proliferation, migration, and invasive potential of prostate cancer cell lines. Cell Cycle. 2011;10(7):1121–31. Zhang Z, Zhang B, Li W, Fu L, Fu L, et al. Epigenetic silencing of miR-203 upregulates SNAI2 and contributes to the invasiveness of malignant breast cancer cells. Genes Cancer. 2011;2(8):782–91. Wang W, Wanjun L, Hui S, Dongyue C, Xinjun Y, Jisheng Z. miR-203 inhibits proliferation of HCC cells by targeting Survivn. Cell Biochem Funct. 2013;31:82–5. Chiang Y, Song Y, Wang Z, Chen Y, Yue Z, Xu H, Xing C, Liu Z. Aberrant expression of miR-203 and its clinical significance in gastric and colorectal cancers. J Gastrointest Surg. 2011;15(1):63–70. Zheng Jiang C, Li Hua H, ShaoJun H. Polymorphism of survivin promoter regions—31 g/C and gastric cancer. Cancer. 2008;27(3):258–63. Ulukus EC, Kargi HA, Sis B, Lebe B, Oztop I, et al. Survivin expression in non-small-cell lung carcinomas: correlation with apoptosis and other apoptosis-related proteins, clinicopathologic prognostic factors and prognosis. Applied Immunohistochemistry &Molecular Morphology. 2007;15:31–7. Karam JA, Lotan Y, Ashfaq R, Sagalowsky AI, Shariat SF. Survivin expression in patients with non-muscle-invasive urothelial cell carcinoma of the bladder. Urology. 2007;70:482–6. Li QX, CongYa Y, XiaoLu Y, et al. FGFR1 and survivin expression analysis of clinical significance in breast infiltrating ductal carcinoma tissue. Chinese Journal of Cancer Prevention and Treatment. 2013;20(17):1315–22. Yan Z, QiChang Y, HongBing L, et al. The expression of osteopontin, survivin and BCL—2 and clinical significance of cervical lesions. Cancer Research on Prevention and Treatment. 2013;4(1):83–6. Zhou XL, Lin CC. Survivin and angiotensin-converting enzyme polymorphisms with risk of colorectal cancer; a systematic review and meta-analysis. World J Surg Oncol. 2015;13:27.