The Mechanism of DNA Methylation and miRNA in Breast Cancer

被引:13
|
作者
Ma, Lingyuan [1 ,2 ]
Li, Chenyu [1 ,2 ]
Yin, Hanlin [1 ,2 ]
Huang, Jiashu [1 ,2 ]
Yu, Shenghao [1 ,2 ]
Zhao, Jin [1 ,2 ]
Tang, Yongxu [1 ,2 ]
Yu, Min [1 ,2 ]
Lin, Jie [1 ,2 ]
Ding, Lei [1 ,2 ]
Cui, Qinghua [1 ,2 ]
机构
[1] Yunnan Univ, Sch Life Sci, Lab Biochem & Mol Biol, Kunming 650091, Peoples R China
[2] Yunnan Collaborat Innovat Ctr Plateau Lake Ecol &, Kunming 650214, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; DNA methylation; miRNA; drug resistance; ESTROGEN-RECEPTOR-ALPHA; PROMOTER METHYLATION; DRUG-RESISTANCE; CISPLATIN RESISTANCE; MICRORNA GENES; HYPOMETHYLATION; CELLS; OVEREXPRESSION; EPIGENETICS; INVASION;
D O I
10.3390/ijms24119360
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer is the most prevalent cancer in the world. Currently, the main treatments for breast cancer are radiotherapy, chemotherapy, targeted therapy and surgery. The treatment measures for breast cancer depend on the molecular subtype. Thus, the exploration of the underlying molecular mechanisms and therapeutic targets for breast cancer remains a hotspot in research. In breast cancer, a high level of expression of DNMTs is highly correlated with poor prognosis, that is, the abnormal methylation of tumor suppressor genes usually promotes tumorigenesis and progression. MiRNAs, as non-coding RNAs, have been identified to play key roles in breast cancer. The aberrant methylation of miRNAs could lead to drug resistance during the aforementioned treatment. Therefore, the regulation of miRNA methylation might serve as a therapeutic target in breast cancer. In this paper, we reviewed studies on the regulatory mechanisms of miRNA and DNA methylation in breast cancer from the last decade, focusing on the promoter region of tumor suppressor miRNAs methylated by DNMTs and the highly expressed oncogenic miRNAs inhibited by DNMTs or activating TETs.
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页数:16
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