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G蛋白偶联受体粘附家族与癌症

Adhesion family of G protein-coupled receptors and cancer.

作者信息

Lin Hsi-Hsien

机构信息

Department of Microbiology and Immunology, College of Medicine, Chang Gung University, Taoyuan, Taiwan.

出版信息

Chang Gung Med J. 2012 Jan-Feb;35(1):15-27. doi: 10.4103/2319-4170.106170.

Abstract

The adhesion-class G protein-coupled receptors (adhesion-GPCRs) constitute the second largest GPCR sub-family in humans. Adhesion-GPCRs are defined by the chimeric structure of an unusually large extracellular cell-adhesion domain and a GPCR-like seven-pass transmembrane domain. Adhesion-GPCRs are hence expected to display both cellular adhesion and signaling functions in many biological systems. Adhesion-GPCRs are normally expressed in the central nervous, immune, and reproductive systems in a cell type- or tissue-restricted fashion. However, aberrant expression of distinct adhesion-GPCR molecules has been identified in various human cancers with some of the receptors closely associated with cancer development. Tumor-associated adhesion-GPCRs are thought to involve in tumorigenesis by affecting the growth of tumor cells, angiogenesis, tumor cell migration, invasion and metastasis either positively or negatively. Furthermore, some adhesion-GPCRs are considered potential biomarkers for specific types of cancers. In this review article, the expressional characteristics and functional role of cancer-associated adhesion-GPCRs are discussed in depth.

摘要

粘附类G蛋白偶联受体(粘附-GPCRs)构成了人类中第二大的GPCR亚家族。粘附-GPCRs由一个异常大的细胞外细胞粘附结构域和一个类似GPCR的七次跨膜结构域的嵌合结构所定义。因此,粘附-GPCRs有望在许多生物系统中发挥细胞粘附和信号传导功能。粘附-GPCRs通常以细胞类型或组织受限的方式在中枢神经、免疫和生殖系统中表达。然而,在各种人类癌症中已发现不同的粘附-GPCR分子存在异常表达,其中一些受体与癌症发展密切相关。肿瘤相关的粘附-GPCRs被认为通过正向或负向影响肿瘤细胞的生长、血管生成、肿瘤细胞迁移、侵袭和转移而参与肿瘤发生。此外,一些粘附-GPCRs被认为是特定类型癌症的潜在生物标志物。在这篇综述文章中,将深入讨论癌症相关粘附-GPCRs的表达特征和功能作用。

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