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MicroRNA dysregulation in gastric cancer: a new player enters the game
被引:0
|作者:
W K K Wu
C W Lee
C H Cho
D Fan
K Wu
J Yu
J J Y Sung
机构:
[1] Institute of Digestive Diseases,LKS Institute of Health Sciences and Department of Medicine and Therapeutics
[2] The Chinese University of Hong Kong,undefined
[3] School of Biomedical Sciences,undefined
[4] Faculty of Medicine,undefined
[5] The Chinese University of Hong Kong,undefined
[6] State Key Laboratory of Cancer Biology and Institute of Digestive Diseases,undefined
[7] Xijing Hospital,undefined
[8] Fourth Military Medical University,undefined
来源:
Oncogene
|
2010年
/
29卷
关键词:
microRNA;
gastric cancer;
signaling pathway;
proliferation;
apoptosis;
metastasis;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Gastric carcinogenesis is a multistep process involving genetic and epigenetic alteration of protein-coding proto-oncogenes and tumor-suppressor genes. Recent discoveries have shed new light on the involvement of a class of noncoding RNA known as microRNA (miRNA) in gastric cancer. A substantial number of miRNAs show differential expression in gastric cancer tissues. Genes coding for these miRNAs have been characterized as novel proto-oncogenes and tumor-suppressor genes based on findings that these miRNAs control malignant phenotypes of gastric cancer cells. In this connection, miRNA dysregulation promotes cell-cycle progression, confers resistance to apoptosis, and enhances invasiveness and metastasis. Moreover, certain polymorphisms in miRNA genes are associated with increased risks for atrophic gastritis and gastric cancer, whereas circulating levels of miRNAs may serve as biomarkers for early diagnosis. Several miRNAs have also been shown to correlate with gastric cancer progression, and thus may be used as prognostic markers. Elucidating the biological aspects of miRNA dysregulation may help us better understand the pathogenesis of gastric cancer and promote the development of miRNA-directed therapeutics against this deadly disease.
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页码:5761 / 5771
页数:10
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