MicroRNA dysregulation as a prognostic biomarker in colorectal cancer

被引:80
作者
Dong, Yujuan [1 ,2 ]
Yu, Jun [2 ]
Ng, Simon S. M. [1 ,2 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Surg, Div Colorectal Surg, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, State Key Lab Digest Dis, Inst Digest Dis, Hong Kong, Hong Kong, Peoples R China
关键词
microRNA; colorectal cancer; prognostic biomarker; single-nucleotide polymorphism; microsatellite instability; BINDING SITE POLYMORPHISM; 3' UNTRANSLATED REGION; II COLON-CANCER; WILD-TYPE KRAS; POOR-PROGNOSIS; DOWN-REGULATION; MICROSATELLITE INSTABILITY; CLINICAL-SIGNIFICANCE; EXPRESSION PROFILES; RECTAL-CANCER;
D O I
10.2147/CMAR.S35164
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is one of the most potentially curable cancers, yet it remains the fourth most common overall cause of cancer death worldwide. The identification of robust molecular prognostic biomarkers can refine the conventional tumor-node-metastasis staging system, avoid understaging of tumor, and help pinpoint patients with early-stage CRC who may benefit from aggressive treatments. Recently, epigenetic studies have provided new molecular evidence to better categorize the CRC subtypes and predict clinical outcomes. In this review, we summarize recent findings concerning the prognostic potential of microRNAs (miRNAs) in CRC. We first discuss the prognostic value of three tissue miRNAs (miR-21-5p, miR-29-3p, miR-148-3p) that have been examined in multiple studies. We also summarize the dysregulation of miRNA processing machinery DICER in CRC and its association with risk for mortality. We also reviewe the potential application of miRNA-associated single-nucleotide polymorphisms as prognostic biomarkers for CRC, especially the miRNA-associated polymorphism in the KRAS gene. Last but not least, we discuss the microsatellite instability-related miRNA candidates. Among all these candidates, miR-21-5p is the most promising prognostic marker, yet further prospective validation studies are required before it can go into clinical usage.
引用
收藏
页码:405 / 422
页数:18
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