Jinbo Fang, Huali Xu, Chunshu Yang, Shubha Kayarthodi, Roland Matthews, Veena N Rao, E Shyam P Reddy
{"title":"Molecular Mechanism of Activation of Transforming Growth Factor Beta/Smads Signaling Pathway in Ets Related Gene-Positive Prostate Cancers.","authors":"Jinbo Fang, Huali Xu, Chunshu Yang, Shubha Kayarthodi, Roland Matthews, Veena N Rao, E Shyam P Reddy","doi":"10.1166/jpsp.2014.1008","DOIUrl":null,"url":null,"abstract":"<p><p>Transforming growth factor beta (TGF-β) signaling pathway is involved in diverse cellular processes, including cell proliferation, differentiation, adhesion, apoptosis, and some human diseases including cancer. Smad proteins function as mediators of intracellular signal transduction of TGF-β. Following their phosphorylation by TGF-β receptor I, Smad2 and Smad3 form a heteromeric complex with Smad4 and then are translocated into the nucleus where they bind to other co-factors and regulate the expression of target genes. ERG (Ets Related Gene) belongs to the ETS family of transcriptional factors. Chromosomal rearrangement of TMPRSS2 gene and ERG gene has been found in the majority of prostate cancers. Over-expression of full length or truncated ERG proteins is associated with a higher rate of recurrence and unfavorable prognosis. In this review, we focus on recent understanding of regulation of TGF-β/Smads signaling pathway by ERG proteins in prostate cancer.</p>","PeriodicalId":90906,"journal":{"name":"Journal of pharmaceutical sciences and pharmacology","volume":"1 1","pages":"82-85"},"PeriodicalIF":0.0000,"publicationDate":"2014-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1166/jpsp.2014.1008","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of pharmaceutical sciences and pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1166/jpsp.2014.1008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12
Abstract
Transforming growth factor beta (TGF-β) signaling pathway is involved in diverse cellular processes, including cell proliferation, differentiation, adhesion, apoptosis, and some human diseases including cancer. Smad proteins function as mediators of intracellular signal transduction of TGF-β. Following their phosphorylation by TGF-β receptor I, Smad2 and Smad3 form a heteromeric complex with Smad4 and then are translocated into the nucleus where they bind to other co-factors and regulate the expression of target genes. ERG (Ets Related Gene) belongs to the ETS family of transcriptional factors. Chromosomal rearrangement of TMPRSS2 gene and ERG gene has been found in the majority of prostate cancers. Over-expression of full length or truncated ERG proteins is associated with a higher rate of recurrence and unfavorable prognosis. In this review, we focus on recent understanding of regulation of TGF-β/Smads signaling pathway by ERG proteins in prostate cancer.
转化生长因子β (TGF-β)信号通路参与多种细胞过程,包括细胞增殖、分化、粘附、凋亡,以及包括癌症在内的一些人类疾病。Smad蛋白是TGF-β细胞内信号转导的介质。在被TGF-β受体I磷酸化后,Smad2和Smad3与Smad4形成异质复合物,然后易位到细胞核中,与其他辅助因子结合并调节靶基因的表达。ERG (Ets Related Gene)属于Ets转录因子家族。在大多数前列腺癌中发现TMPRSS2基因和ERG基因的染色体重排。全长或截短ERG蛋白的过表达与较高的复发率和不良预后相关。本文就ERG蛋白在前列腺癌中调控TGF-β/Smads信号通路的研究进展进行综述。