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结直肠癌和胃癌中的p300基因改变。

p300 gene alterations in colorectal and gastric carcinomas.

作者信息

Muraoka M, Konishi M, Kikuchi-Yanoshita R, Tanaka K, Shitara N, Chong J M, Iwama T, Miyaki M

机构信息

Department of Biochemistry, Tokyo Metropolitan Institute of Medical Science, Japan.

出版信息

Oncogene. 1996 Apr 4;12(7):1565-9.

PMID:8622873
Abstract

Colorectal tumors frequently have loss of heterozygosity on chromosome 22q, suggesting that inactivation of tumor suppressor gene(s) on 22q participates in the tumor development. Neurofibromatosis 2 (NF2) gene and E1A binding protein p300 gene, recently identified on 22q, are thought to be candidates for tumor suppressor genes. In this study, mutation of the NF2 gene in 59 colorectal carcinomas, and mutation of the p300 gene in 27 colorectal and two gastric carcinomas, were analysed using PCR-SSCP, RT-PCR-SSCP and direct sequencing methods. Missense mutations of p300 gene were detected in a colorectal carcinoma, and in a gastric carcinoma, though no mutation of NF2 gene was detected. Both p300 mutations were somatic and coupled to deletion of the second allele of the gene, which suggests inactivation of the p300 gene, in these carcinomas. The mutations are located within the Cys/His-rich regions, which are assumed to play important roles in the function of p300. These are the first cases in which p300 gene has been found to be altered in both alleles, suggesting that inactivation of the p300 gene may be involved in the development of carcinomas, and that this gene may be the target of loss of 22q in carcinomas of the digestive tract.

摘要

结直肠肿瘤在22号染色体上经常出现杂合性缺失,这表明22号染色体上肿瘤抑制基因的失活参与了肿瘤的发生发展。最近在22号染色体上发现的神经纤维瘤病2(NF2)基因和E1A结合蛋白p300基因被认为是肿瘤抑制基因的候选者。在本研究中,使用PCR-SSCP、RT-PCR-SSCP和直接测序方法分析了59例结直肠癌中NF2基因的突变,以及27例结直肠癌和2例胃癌中p300基因的突变。在1例结直肠癌和1例胃癌中检测到了p300基因的错义突变,而未检测到NF2基因的突变。这两个p300突变均为体细胞突变,且与该基因第二个等位基因的缺失相关,这表明在这些癌症中p300基因失活。这些突变位于富含半胱氨酸/组氨酸的区域内,推测该区域在p300的功能中起重要作用。这是首次发现p300基因两个等位基因均发生改变的病例,提示p300基因失活可能参与了癌症的发生发展,并且该基因可能是消化道癌症中22号染色体缺失的靶点。

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