INACTIVATION OF THE TYPE-II TGF-BETA RECEPTOR IN COLON-CANCER CELLS WITH MICROSATELLITE INSTABILITY

被引:2101
作者
MARKOWITZ, S
WANG, J
MYEROFF, L
PARSONS, R
SUN, LZ
LUTTERBAUGH, J
FAN, RS
ZBOROWSKA, E
KINZLER, KW
VOGELSTEIN, B
BRATTAIN, M
WILLSON, JKV
机构
[1] UNIV CLEVELAND HOSP, IRELAND CANC CTR, CLEVELAND, OH 44106 USA
[2] CASE WESTERN RESERVE UNIV, CLEVELAND, OH 44106 USA
[3] MED COLL OHIO, DEPT BIOCHEM & MOLEC BIOL, TOLEDO, OH 43699 USA
[4] JOHNS HOPKINS UNIV, CTR ONCOL, BALTIMORE, MD 21231 USA
[5] HOWARD HUGHES MED INST, CHEVY CHASE, MD 20815 USA
关键词
D O I
10.1126/science.7761852
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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收藏
页码:1336 / 1338
页数:3
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