The Discovery and Early Days of TGF-β: A Historical Perspective

  1. Rik Derynck3
  1. 1Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232
  2. 2Laboratory of Cell Regulation and Carcinogenesis, National Cancer Institute, Bethesda, Maryland 20892
  3. 3Department of Cell and Tissue Biology, University of California, San Francisco, California 94143
  1. Correspondence: rik.derynck{at}ucsf.edu
  • 4 Deceased.

Abstract

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.



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      1. Cold Spring Harb. Perspect. Biol. 8: a021865 Copyright © 2016 Cold Spring Harbor Laboratory Press; all rights reserved

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