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作为结直肠癌预后生物标志物的微小RNA表达分析

Expression analysis of microRNA as prognostic biomarkers in colorectal cancer.

作者信息

Yang Jie, Ma Dongling, Fesler Andrew, Zhai Haiyan, Leamniramit Apisri, Li Wenzhe, Wu Song, Ju Jingfang

机构信息

Department of Family, Population and Preventive Medicine, Stony Brook, NY 11794, USA.

The NMS Laboratory, Stony Brook University, Stony Brook, NY, 11794, USA.

出版信息

Oncotarget. 2016 Dec 26;8(32):52403-52412. doi: 10.18632/oncotarget.14175. eCollection 2017 Aug 8.

Abstract

microRNA (miRNA) based biomarkers have unique advantages due to their critical regulatory function, superior stability, and relatively small number compared to mRNAs. A number of miRNAs play key roles in colon cancer stem cell chemoresistance and have clinical potential as prognostic biomarkers. The purpose of this study is to systematically validate the prognostic potential of miRNAs in colorectal cancer. In this study, we validated the prognostic potential of a panel of miRNAs using 205 stage II, III, and IV colorectal cancer specimens by qRT-PCR analysis. We cross validated our results using The Cancer Genome Atlas (TCGA) database. Many of the miRNAs we investigated have been functionally validated to be important in contributing to chemoresistance to 5-fluorouracil (5-FU) based chemotherapy. We determined that miR-16 is the most consistent miRNA for expression normalization in colorectal cancer. We have validated several miRNAs (miR-15b, miR-215, miR-145, miR-192, let-7g) that are significantly associated with progression free survival (PFS) and/or overall survival (OS) of colorectal cancer patients independent of tumor stage and age at diagnosis. These 5 miRNAs are significantly associated with OS of colorectal cancer even after tumor location (left side vs. right side) is adjusted for. Furthermore, the prognostic value of let-7g for overall survival was independently validated using the RNA-Seq results from TCGA colorectal cancer database. These results, taken together, establish a solid foundation towards miRNA based precision management of colorectal cancer.

摘要

基于微小RNA(miRNA)的生物标志物具有独特优势,这归因于其关键的调控功能、卓越的稳定性以及与信使核糖核酸(mRNA)相比数量相对较少。许多miRNA在结肠癌干细胞化疗耐药中发挥关键作用,并具有作为预后生物标志物的临床潜力。本研究的目的是系统验证miRNA在结直肠癌中的预后潜力。在本研究中,我们通过定量逆转录聚合酶链反应(qRT-PCR)分析,使用205例II、III和IV期结直肠癌标本验证了一组miRNA的预后潜力。我们使用癌症基因组图谱(TCGA)数据库对结果进行了交叉验证。我们研究的许多miRNA已在功能上被验证对基于5-氟尿嘧啶(5-FU)的化疗耐药起重要作用。我们确定miR-16是结直肠癌中用于表达标准化最一致的miRNA。我们验证了几种与结直肠癌患者无进展生存期(PFS)和/或总生存期(OS)显著相关的miRNA(miR-15b、miR-215、miR-145、miR-192、let-7g),其与肿瘤分期和诊断时年龄无关。即使在调整肿瘤位置(左侧与右侧)后,这5种miRNA仍与结直肠癌的OS显著相关。此外,使用TCGA结直肠癌数据库的RNA测序结果独立验证了let-7g对总生存期的预后价值。综上所述,这些结果为基于miRNA的结直肠癌精准管理奠定了坚实基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93b5/5581037/94d47526a7b5/oncotarget-08-52403-g001.jpg

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