期刊
TRENDS IN PHARMACOLOGICAL SCIENCES
卷 33, 期 7, 页码 382-393出版社
ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tips.2012.04.003
关键词
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资金
- Hungarian Ministry of National Resources [ETT40/09]
- Janos Bolyai Research Fellowship
- [TAMOP-4.2.2.B-10/B-10/1-2010-0013]
The activin/transforming growth factor-beta (TGF-beta) pathway plays an important role in tumorigenesis either by its tumor suppressor or tumor promoting effect. Loss of members of the TGF-beta signaling by somatic mutations or epigenetic events, such as DNA methylation or regulation by microRNA (miRNA), may affect the signaling process. Most members of the TGF-beta pathway are known to be targeted by one or more miRNAs. In addition, the biogenesis of miRNAs is also regulated by TGF-beta both directly and through SMADs. Based on these interactions, it appears that autoregulatory feedback loops between TGF-beta and miRNAs influence the fate of tumor cells. Our aim is to review the crosstalk between TGF-beta signaling and the miRNA machinery to highlight potential novel therapeutic targets.
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