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睾丸癌和前列腺癌中的干细胞因子(SCF)/c-KIT信号传导

The stem cell factor (SCF)/c-KIT signalling in testis and prostate cancer.

作者信息

Cardoso Henrique J, Figueira Marília I, Socorro Sílvia

机构信息

CICS-UBI, Centro de Investigação em Ciências da Saúde, Universidade da Beira Interior, Av. Infante D. Henrique, 6200-506, Covilhã, Portugal.

出版信息

J Cell Commun Signal. 2017 Dec;11(4):297-307. doi: 10.1007/s12079-017-0399-1. Epub 2017 Jun 27.

Abstract

The stem cell factor (SCF) is a cytokine that specifically binds the tyrosine kinase receptor c-KIT. The SCF/c-KIT interaction leads to receptor dimerization, activation of kinase activity and initiation of several signal transduction pathways that control cell proliferation, apoptosis, differentiation and migration in several tissues. The activity of SCF/c-KIT system is linked with the phosphatidylinositol 3-kinase (PI3-K), the Src, the Janus kinase/signal transducers and activators of transcription (JAK/STAT), the phospholipase-C (PLC-γ) and the mitogen-activated protein kinase (MAPK) pathways. Moreover, it has been reported that cancer cases display an overactivation of c-KIT due to the presence of gain-of-function mutations or receptor overexpression, which renders c-KIT a tempting target for cancer treatment. In the case of male cancers the most documented activated pathways are the PI3-K and Src, both enhancing abnormal cell proliferation. It is also known that the Src activity in prostate cancer cases depends on the presence of tr-KIT, the cytoplasmic truncated variant of c-KIT that is specifically expressed in tumour tissues and, thus, a very interesting target for drug development. The present review provides an overview of the signalling pathways activated by SCF/c-KIT and discusses the potential application of c-KIT inhibitors for treatment of testicular and prostatic cancers.

摘要

干细胞因子(SCF)是一种细胞因子,它能特异性结合酪氨酸激酶受体c-KIT。SCF/c-KIT相互作用导致受体二聚化、激酶活性激活,并启动多种信号转导途径,这些途径控制着多种组织中的细胞增殖、凋亡、分化和迁移。SCF/c-KIT系统的活性与磷脂酰肌醇3激酶(PI3-K)、Src、Janus激酶/信号转导子和转录激活子(JAK/STAT)、磷脂酶-C(PLC-γ)和丝裂原活化蛋白激酶(MAPK)途径相关。此外,据报道,由于功能获得性突变的存在或受体过表达,癌症病例中c-KIT会过度激活,这使得c-KIT成为癌症治疗的一个诱人靶点。在男性癌症中,记录最多的激活途径是PI3-K和Src,两者都增强异常细胞增殖。还已知前列腺癌病例中的Src活性取决于tr-KIT的存在,tr-KIT是c-KIT的细胞质截短变体,在肿瘤组织中特异性表达,因此是药物开发中一个非常有趣的靶点。本综述概述了SCF/c-KIT激活的信号通路,并讨论了c-KIT抑制剂在睾丸癌和前列腺癌治疗中的潜在应用。

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