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Wnt与肿瘤发生的关联。

The Wnt connection to tumorigenesis.

作者信息

Behrens Jürgen, Lustig Barbara

机构信息

Nikolaus-Fiebiger-Center for Molecular Medicine, University Erlangen-N rnberg, 91054 Erlangen, Germany.

出版信息

Int J Dev Biol. 2004;48(5-6):477-87. doi: 10.1387/ijdb.041815jb.

Abstract

Wnt signaling has been identified as one of the key signaling pathways in cancer, regulating cell growth, motility and differentiation. Because of its widespread activation in diverse human tumor diseases, the Wnt pathway has gained considerable and growing interest in tumor research over recent years. Evidence that altered Wnt signaling is important for human tumor development came from three major findings: (i) the tumor suppressor adenomatous polyposis coli (APC) binds to the Wnt pathway component beta-catenin and is involved in its degradation, (ii) mutations of APC in colon tumors lead to stabilization of the beta-catenin protein and (iii) tumor-associated mutations of beta-catenin in colorectal cancer as well as in other tumor types lead to its stabilisation, qualifying beta-catenin as a proto-oncogene. Here we will describe the biochemical interactions which shape the Wnt pathway and focus on its role in tumorigenesis.

摘要

Wnt信号通路已被确认为癌症中的关键信号通路之一,可调节细胞生长、运动和分化。由于其在多种人类肿瘤疾病中广泛激活,近年来Wnt通路在肿瘤研究中引起了越来越多的关注。Wnt信号改变对人类肿瘤发展至关重要的证据来自三个主要发现:(i)肿瘤抑制因子腺瘤性息肉病 coli(APC)与Wnt通路成分β-连环蛋白结合并参与其降解,(ii)结肠肿瘤中APC的突变导致β-连环蛋白蛋白的稳定,以及(iii)结直肠癌和其他肿瘤类型中β-连环蛋白的肿瘤相关突变导致其稳定,使β-连环蛋白成为原癌基因。在这里,我们将描述塑造Wnt通路的生化相互作用,并重点关注其在肿瘤发生中的作用。

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