Current perspectives of mi-RNA in oesophageal adenocarcinoma: Roles in predicting carcinogenesis, progression and values in clinical management

被引:28
作者
Amin, Moein [1 ,2 ]
Lam, Alfred King-yin [1 ,2 ,3 ]
机构
[1] Griffith Univ, Sch Med, Canc Mol Pathol, Gold Coast, Qld, Australia
[2] Griffith Univ, Menzies Hlth Inst, Queensland Inst, Gold Coast, Qld, Australia
[3] Gold Coast Univ Hosp, Pathol Queensland, Gold Coast, Qld, Australia
关键词
Micro-RNA; Oesophageal adenocarcinoma; Metastases; Prognosis; SQUAMOUS-CELL-CARCINOMA; MICRORNA EXPRESSION; BARRETTS-ESOPHAGUS; TELOMERASE ACTIVITY; GLEDITSIA-SINENSIS; CANCER; GENE; OVEREXPRESSION; SURVIVAL; FAMILY;
D O I
10.1016/j.yexmp.2015.03.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aberrant expressions of micro-ribonucleic acids (miRs) are closely associated with the pathogenesis in many human cancers. In oesophageal adenocarcinomas, altered expressions of different sets of miRs are noted to be associated with the development of adenocarcinoma from Barrett's oesophagus. In different studies, miRs such as miR-192, miR-196 and miR-21 were frequently noted to up-regulated whereas miR-203, miR-205 and miR-let-7 were commonly down-regulated during the development of Barrett's oesophagus to oesophageal adenocarcinoma. In addition, changes in the expression of miRs are associated with the predication of metastasis, prognosis and response to chemo-radiation in the patients with oesophageal adenocarcinoma. Experimental studies in manipulating the miRs in cancer cell lines could provide hints for therapeutics for the cancer. However, the number of studies reported on these aspects of oesophageal adenocarcinoma was limited and the miRs noted needed to be confirmed by additional studies. Overall, the mechanisms of involvements of miRs in pathogenesis and progression of oesophageal adenocarcinoma are complex. Although miRs have the potential to act as prognostic and clinical biomarkers for cancer therapy in oesophageal adenocarcinoma, more works in larger populations and clinical trials are needed to validate these clinical implications. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:411 / 418
页数:8
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