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家族性腺瘤性息肉病(FAP)患者及散发性结直肠癌肿瘤中APC(腺瘤性息肉病 coli)基因的突变。

Mutations of the APC (adenomatous polyposis coli) gene in FAP (familial polyposis coli) patients and in sporadic colorectal tumors.

作者信息

Nakamura Y, Nishisho I, Kinzler K W, Vogelstein B, Miyoshi Y, Miki Y, Ando H, Horii A

机构信息

Department of Biochemistry, Cancer Institute, Tokyo, Japan.

出版信息

Tohoku J Exp Med. 1992 Oct;168(2):141-7. doi: 10.1620/tjem.168.141.

Abstract

We have isolated several genes on chromosome 5q21 region tightly linked to hereditary familial polyposis coli (FAP) and Gardner's syndrome (GS). Two of these genes (MCC and APC) were found to be somatically altered by point mutation, deletion or insertion in tumors of sporadic colorectal cancer patients. One (APC) of them was also found mutations in the germ line of both APC and GS patients. The identification of these genes has significant implications for understanding the pathogenesis of colorectal neoplasia and for the diagnosis and counseling of individuals with inherited predispositions to colorectal cancer.

摘要

我们已经在5号染色体q21区域分离出了几个与遗传性家族性结肠息肉病(FAP)和加德纳综合征(GS)紧密连锁的基因。其中两个基因(MCC和APC)在散发性结直肠癌患者的肿瘤中被发现因点突变、缺失或插入而发生体细胞改变。其中一个基因(APC)在APC和GS患者的生殖系中也被发现有突变。这些基因的鉴定对于理解结直肠癌的发病机制以及对有遗传性结直肠癌易感性个体的诊断和咨询具有重要意义。

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