Targeting miR-375 in gastric cancer

被引:33
|
作者
Xu, Yanjun [1 ]
Deng, Yujie [1 ]
Yan, Xiaoyi [1 ]
Zhou, Tianhua [1 ]
机构
[1] Zhejiang Univ, Sch Med, Dept Cell Biol, Program Mol Cell Biol, Hangzhou 310058, Zhejiang, Peoples R China
关键词
gastric cancer; JAK2; miR-375; miRNA; PDK1; 3-PHOSPHOINOSITIDE-DEPENDENT PROTEIN KINASE-1; TUMOR-SUPPRESSIVE MICRORNAS; CELL-PROLIFERATION; MIR-200; FAMILY; HELICOBACTER-PYLORI; TYROSINE KINASE; DOWN-REGULATION; BREAST-CANCER; MESENCHYMAL TRANSITION; MULTIDRUG-RESISTANCE;
D O I
10.1517/14728222.2011.581232
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Gastric cancer remains a major cancer burden in the world, with a poor 5-year survival rate. It is necessary to develop new effective therapeutic strategies to improve the long-term clinical outcome. MicroRNA (miRNA), a class of small non-coding RNA, has been identified as a key regulator of gene expression, and is implicated in the pathogenesis of gastric cancer. Areas covered: This review summarizes the role of miRNAs in gastric carcinogenesis, with an emphasis on the expression and function of miR-375 in gastric cancer and beyond. It also discusses the opportunities and challenges of miR-375 as a potential therapeutic target for gastric cancer. The genes targeted by miR-375, including JAK2 and 3'-phosphoinositide dependent protein kinase-1 (PDK1), are also candidates for gastric cancer therapy. Expert opinion: Although radical surgery and rational chemotherapy are still the main treatment for gastric cancer, targeting miRNAs, in combination with other conventional therapies, may serve as a promising therapy strategy to improve the clinical outcome.
引用
收藏
页码:961 / 972
页数:12
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