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TMEFF2 的脱落受氧化应激调节,并通过 ADAMs 和跨膜丝氨酸蛋白酶介导,这些蛋白酶与前列腺癌有关。

TMEFF2 shedding is regulated by oxidative stress and mediated by ADAMs and transmembrane serine proteases implicated in prostate cancer.

机构信息

School of Medicine, University of Information Technology and Management in Rzeszow, 2 Sucharskiego Str., 35-225 Rzeszow, Poland.

School of Dentistry, College of Biomedical and Life Sciences, Cardiff University, Cardiff, CF14 4XY, United Kingdom.

出版信息

Cell Biol Int. 2018 Mar;42(3):273-280. doi: 10.1002/cbin.10832. Epub 2017 Aug 21.

Abstract

TMEFF2 is a type I transmembrane protein with two follistatin (FS) and one EGF-like domain over-expressed in prostate cancer; however its biological role in prostate cancer development and progression remains unclear, which may, at least in part, be explained by its proteolytic processing. The extracellular part of TMEFF2 (TMEFF2-ECD) is cleaved by ADAM17 and the membrane-retained fragment is further processed by the gamma-secretase complex. TMEFF2 shedding is increased with cell crowding, a condition associated with the tumour microenvironment, which was mediated by oxidative stress signalling, requiring jun-kinase (JNK) activation. Moreover, we have identified that TMEFF2 is also a novel substrate for other proteases implicated in prostate cancer, including two ADAMs (ADAM9 and ADAM12) and the type II transmembrane serine proteinases (TTSPs) matriptase-1 and hepsin. Whereas cleavage by ADAM9 and ADAM12 generates previously identified TMEFF2-ECD, proteolytic processing by matriptase-1 and hepsin produced TMEFF2 fragments, composed of TMEFF2-ECD or FS and/or EGF-like domains as well as novel membrane retained fragments. Differential TMEFF2 processing from a single transmembrane protein may be a general mechanism to modulate transmembrane protein levels and domains, dependent on the repertoire of ADAMs or TTSPs expressed by the target cell.

摘要

TMEFF2 是一种 I 型跨膜蛋白,在前列腺癌中过表达两种卵泡抑素 (FS) 和一个 EGF 样结构域;然而,其在前列腺癌发生和发展中的生物学作用尚不清楚,这至少部分可以解释为其蛋白水解加工。TMEFF2 的细胞外部分(TMEFF2-ECD)被 ADAM17 切割,膜保留片段被 γ-分泌酶复合物进一步加工。TMEFF2 的脱落随着细胞拥挤而增加,细胞拥挤是与肿瘤微环境相关的条件,这是由氧化应激信号介导的,需要 jun-kinase (JNK) 激活。此外,我们已经确定 TMEFF2 也是其他与前列腺癌相关的蛋白酶的新型底物,包括两种 ADAMs(ADAM9 和 ADAM12)和 II 型跨膜丝氨酸蛋白酶 (TTSP) 组织蛋白酶-1 和 hepsin。虽然 ADAM9 和 ADAM12 的切割产生了先前鉴定的 TMEFF2-ECD,但 matriptase-1 和 hepsin 的蛋白水解处理产生了 TMEFF2 片段,由 TMEFF2-ECD 或 FS 和/或 EGF 样结构域以及新型膜保留片段组成。来自单个跨膜蛋白的差异 TMEFF2 加工可能是一种依赖于靶细胞表达的 ADAMs 或 TTSP 谱来调节跨膜蛋白水平和结构域的通用机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a5/5836882/30ff866409d8/CBIN-42-273-g001.jpg

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