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Inactivation of the Type II TGF-β Receptor in Colon Cancer Cells with Microsatellite Instability

SciencePublished 2 June 1995
Sanford D. Markowitz, Jing Wang, Lois L. Myeroff, Ramon Parsons, Lu‐Zhe Sun, James Lutterbaugh
Citations2,270
SJR quartileQ1
SJR score10.42
SNIP6.62

TL;DR

Human colon cancer cell lines with high rates of microsatellite instability were found to harbor mutations in the type II TGF-beta receptor (RII) gene, which links DNA repair defects with a specific pathway of tumor progression.

Abstract

Transforming growth factor-beta (TGF-beta) is a potent inhibitor of epithelial cell growth. Human colon cancer cell lines with high rates of microsatellite instability were found to harbor mutations in the type II TGF-beta receptor (RII) gene. Eight such examples, due to three different mutations, were identified. The mutations were clustered within small repeated sequences in the RII gene, were accompanied by the absence of cell surface RII receptors, and were usually associated with small amounts of RII transcript. RII mutation, by inducing the escape of cells from TGF-beta-mediated growth control, links DNA repair defects with a specific pathway of tumor progression.

Keywords

MedicineBiochemistry, Genetics and Molecular Biology