Moses Harold L, Roberts Anita B, Derynck Rik
Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232.
Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892.
Cold Spring Harb Perspect Biol. 2016 Jul 1;8(7):a021865. doi: 10.1101/cshperspect.a021865.
Transforming growth factors (TGFs) were discovered as activities that were secreted by cancer cells, and later by normal cells, and had the ability to phenotypically and reversibly transform immortalized fibroblasts. TGF-β distinguished itself from TGF-α because it did not bind to the same epidermal growth factor (EGF) receptor as TGF-α and, therefore, acted through different cell-surface receptors and signaling mediators. This review summarizes the discovery of TGF-β, the early developments in its molecular and biological characterization with its many biological activities in different cell and tissue contexts and its roles in disease, the realization that there is a family of secreted TGF-β-related proteins with many differentiation functions in development and activities in normal cell and tissue physiology, and the subsequent identification and characterization of the receptors and effectors that mediate TGF-β family signaling responses.
转化生长因子(TGFs)最初是作为癌细胞分泌的活性物质被发现的,后来发现正常细胞也能分泌,并且具有使永生化成纤维细胞发生表型可逆转化的能力。转化生长因子-β(TGF-β)与转化生长因子-α(TGF-α)不同,因为它不与TGF-α结合相同的表皮生长因子(EGF)受体,因此通过不同的细胞表面受体和信号传导介质发挥作用。本综述总结了TGF-β的发现、其分子和生物学特性的早期进展,包括在不同细胞和组织环境中的多种生物学活性及其在疾病中的作用;认识到存在一个分泌型TGF-β相关蛋白家族,它们在发育中具有许多分化功能,在正常细胞和组织生理学中也有活性;以及随后对介导TGF-β家族信号反应的受体和效应器的鉴定和表征。