Insights into roles of the miR-1, -133 and -206 family in gastric cancer (Review)
Author(s) -
Meng Xie,
D. Alwyn Dart,
Sioned Owen,
Xianzi Wen,
Jiafu Ji,
Wen G. Jiang
Publication year - 2016
Publication title -
oncology reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.094
H-Index - 96
eISSN - 1791-2431
pISSN - 1021-335X
DOI - 10.3892/or.2016.4908
Subject(s) - microrna , cancer , biology , carcinogenesis , oncogene , molecular medicine , cell cycle , metastasis , bioinformatics , cancer research , mechanism (biology) , gene , computational biology , genetics , philosophy , epistemology
Gastric cancer (GC) remains the third most common cause of cancer deaths worldwide and carries a high rate of metastatic risk contributing to the main cause of treatment failure. An accumulation of data has resulted in a better understanding of the molecular network of GC, however, gaps still exist between the unique bio-resources and clinical application. MicroRNAs are an important part of non-coding RNAs and behave as major regulators of tumour biology, alongside their well-known roles as intrinsic factors of gene expression in cellular processes, via their post-transcriptional regulation of components of signalling pathways in a coordinated manner. Deregulation of the miR-1, -133 and -206 family plays a key role in tumorigenesis, progression, invasion and metastasis. This review aims to provide a summary of recent findings on the miR-1, -133 and -206 family in GC and how this knowledge might be exploited for the development of future miRNA-based therapies for the treatment of GC.
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