Transforming growth factor beta type II receptor gene mutations in adenomas from hereditary nonpolyposis colorectal cancer

被引:103
作者
Akiyama, Y
Iwanaga, R
Saitoh, K
Shiba, K
Ushio, K
Ikeda, E
Iwama, T
Nomizu, T
Yuasa, Y
机构
[1] TOKYO MED & DENT UNIV,SCH MED,DEPT HYG & ONCOL,BUNKYO KU,TOKYO 113,JAPAN
[2] TOKYO MED & DENT UNIV,SCH MED,DEPT SURG 2,BUNKYO KU,TOKYO 113,JAPAN
[3] TOKYO MED & DENT UNIV,SCH ALLIED HLTH SCI,TOKYO 113,JAPAN
[4] NATL CANC CTR,DEPT DIAGNOST RADIOL,TOKYO 104,JAPAN
[5] YAMAGATA PREFECTURAL CENT HOSP,DEPT SURG,YAMAGATA,JAPAN
[6] HOSHI GEN HOSP,DEPT SURG,FUKUSHIMA,JAPAN
关键词
D O I
10.1016/S0016-5085(97)70216-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Germline mutations of DNA mismatch repair genes are responsible for cancer susceptibility in hereditary nonpolyposis colorectal cancer (HNPCC) kindreds, Transforming growth factor beta type II receptor (TGF-beta RII) has been found to be somatically altered in HNPCC, The aim of this study was to clarify further the role of TGF-beta RII alterations in HNPCC tumorigenesis, particularly in adenomas, Methods: Fourteen adenoma specimens and 13 cancer specimens from 10 patients with HNPCC were screened for mutations in the short repeated sequences of the TGF-beta RII gene by polymerase chain reaction-single-strand conformation polymorphism. Mismatch repair genes, replication errors, and c-K-ras 2 were also analyzed in HNPCC tumors, Results: Alterations of the TGF-beta RII gene at the short poly(A) repeat were found in 8 (57%) adenoma specimens and 11 (85%) cancer specimens, They were found at an earlier stage of adenomas. Two adenoma specimens showed two-hit inactivation of mismatch repair genes, Replication errors were detectable in 13 (93%) adenoma specimens, Mutations in c-K-ras 2 codon 12 were detected at a 50% frequency in adenoma specimens. Conclusions: These data indicate a strong association between TGF-beta RII gene alterations and adenoma-carcinoma progression in HNPCC.
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页码:33 / 39
页数:7
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