A transforming growth factor beta 1 receptor type II mutation in ulcerative colitis-associated neoplasms

Autor: O. Chan, Barbara A. Leggett, Suna Wang, Joanne Young, Lisa A. Simms, W. S. Park, Xianlong Zhou, Mun-Gan Rhyu, Stephen J. Meltzer, Tontong Zou, John M. Abraham, K. Cymes, Rebecca Appel, Rhonda F. Souza, Mark J. Krasna, John R. Cottrell, Jing Yin, Noam Harpaz, Junyi Lei, Bruce D. Greenwald
Rok vydání: 1997
Předmět:
Zdroj: Gastroenterology. 112:40-45
ISSN: 0016-5085
DOI: 10.1016/s0016-5085(97)70217-8
Popis: BACKGROUND & AIMS: Numerous gastrointestinal tumors, notably sporadic and ulcerative colitis (UC)-associated colorectal carcinomas and dysplasias, gastric cancers, and esophageal carcinomas, manifest microsatellite instability. Recently, a transforming growth factor beta 1 type II receptor (TGF-beta 1RII) mutation in a coding microsatellite was described in colorectal carcinomas showing instability. One hundred thirty-eight human neoplasms (61 UC-associated, 35 gastric, 26 esophageal, and 16 sporadic colorectal) were evaluated for this TGF- beta 1RII mutation. METHODS: Whether instability was present at other chromosomal loci in these lesions was determined. In lesions manifesting or lacking instability, the TGF-beta 1RII coding region polydeoxyadenine (poly A) microsatellite tract was polymerase chain reaction amplified with 32P-labeled deoxycytidine triphosphate. Polymerase chain reaction products were electrophoresed on denaturing gels and exposed to radiographic film. RESULTS: Three of 18 UC specimens with instability at other chromosomal loci (17%) showed TGF- beta 1RII poly A tract mutation, including 2 cancers and 1 dysplasia; moreover, 2% of UC specimens without instability (1 of 43) (1 cancer), 81% of unstable sporadic colorectal cancers (13 of 16), and none of the 61 stable or unstable gastric or esophageal cancers contained TGF-beta 1RII mutations. CONCLUSIONS: Mutational inactivation of the poly A microsatellite tract within TGF-beta 1RII occurs early and in a subset of unstable UC neoplasms and commonly in sporadic colorectal cancers but may be rare in unstable gastric and esophageal tumors. (Gastroenterology 1997 Jan;112(1):40-5)
Databáze: OpenAIRE