DNA ALTERATIONS IN CELLS FROM HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER PATIENTS

被引:0
|
作者
WU, C
AKIYAMA, Y
IMAI, K
MIYAKE, S
NAGASAKI, H
OTO, M
OKABE, S
IWAMA, T
MITAMURA, K
MASUMITSU, H
NOMIZU, T
BABA, S
MARUYAMA, K
YUASA, Y
机构
[1] TOKYO MED & DENT UNIV, SCH MED, DEPT HYG & ONCOL, TOKYO, TOKYO 113, JAPAN
[2] TOKYO MED & DENT UNIV, SCH MED, DEPT SURG, TOKYO, TOKYO 113, JAPAN
[3] SHOWA UNIV, SCH MED, DEPT INTERNAL MED, TOKYO, TOKYO 142, JAPAN
[4] TOKYO METROPOLITAN PUBL HLTH PROMOT FDN, TAMA CANC DETECT CTR, TOKYO, TOKYO 183, JAPAN
[5] HOSHI GEN HOSP, DEPT SURG, FUKUSHIMA, FUKUSHIMA 963, JAPAN
[6] HAMAMATSU UNIV SCH MED, DEPT SURG, HAMAMATSU, SHIZUOKA 43131, JAPAN
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To determine if the MCC, DCC or p53 gene is associated with susceptibility to hereditary non-polyposis colorectal cancer (HNPCC), these genes in normal cells from 12 HNPCC patients were analysed by polymerase chain reaction-single strand conformation polymorphism analysis. No changes which may alter the amino acid sequences of these genes were detected, suggesting that these genes are not associated with the susceptibility to HNPCC. Only one of nine HNPCC cancers showed mutations in the MCC and p53 genes on the same analysis. Loss of heterozygosity in chromosomes 5q, 17p, 18q and 22 was detected in four of the nine cancers, all of them being positive as to metastasis to lymph nodes. Abnormalities of the (CA)n repeat were found in six cancers, including all four without metastasis. These data indicate that tumor suppressor genes in chromosomes 5q, 17p, 18q and 22 are associated with the late stage of colorectal tumorigenesis in HNPCC, whereas the (CA)n repeat abnormalities are an early event of tumorigenesis and more essential to HNPCC.
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页码:991 / 994
页数:4
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