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人结直肠癌中DPC4基因的体细胞改变(体内研究)

Somatic alterations of the DPC4 gene in human colorectal cancers in vivo.

作者信息

Takagi Y, Kohmura H, Futamura M, Kida H, Tanemura H, Shimokawa K, Saji S

机构信息

Department of Surgery II, Gifu University School of Medicine, Japan.

出版信息

Gastroenterology. 1996 Nov;111(5):1369-72. doi: 10.1053/gast.1996.v111.pm8898652.

Abstract

BACKGROUND & AIMS: The chromosome region 18q21 has been shown to be frequently deleted in colorectal cancers, and such frequent allelic loss is a hallmark of the presence of a tumor-suppressor gene. The DPC4 gene, which is located at 18q21, has been identified as a tumor-suppressor gene from examination of pancreatic cancers. The aim of the present study was to determine if it might also be altered in colorectal cancers.

METHODS

Mutation analyses of the DPC4 gene were performed on complementary DNA samples from 31 primary colorectal cancer specimens using a combination of polymerase chain reaction, single-strand conformation polymorphism, and DNA sequencing.

RESULTS

Four missense mutations producing amino acid substitutions and a somatic 12-base pair deletion in the coding region of the DPC4 gene were detected in the 31 cancers (16%; 5 of 31).

CONCLUSIONS

The DPC4 gene may play a role as a tumor-suppressor gene in a fraction of colorectal cancers; however, while allelic loss at 18q21 is very often seen in colorectal cancers, only a minority show DPC4 mutations, suggesting that there might be another tumor-suppressor gene in this chromosome region.

摘要

背景与目的

18q21染色体区域在结直肠癌中常出现缺失,这种频繁的等位基因缺失是肿瘤抑制基因存在的标志。位于18q21的DPC4基因,在胰腺癌研究中已被鉴定为肿瘤抑制基因。本研究的目的是确定其在结直肠癌中是否也会发生改变。

方法

采用聚合酶链反应、单链构象多态性分析和DNA测序相结合的方法,对31例原发性结直肠癌标本的互补DNA样本进行DPC4基因突变分析。

结果

在31例癌症中检测到4个导致氨基酸替换的错义突变和DPC4基因编码区一个体细胞12碱基对的缺失(16%;31例中的5例)。

结论

DPC4基因可能在部分结直肠癌中作为肿瘤抑制基因发挥作用;然而,虽然18q21等位基因缺失在结直肠癌中很常见,但只有少数出现DPC4突变,这表明该染色体区域可能存在另一个肿瘤抑制基因。

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