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原发性胰腺腺癌中CDKN2的频繁突变。

Frequent mutations of CDKN2 in primary pancreatic adenocarcinomas.

作者信息

Bartsch D, Shevlin D W, Tung W S, Kisker O, Wells S A, Goodfellow P J

机构信息

Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Genes Chromosomes Cancer. 1995 Nov;14(3):189-95. doi: 10.1002/gcc.2870140306.

Abstract

The gene encoding the cell-cycle regulatory protein p16, CDKN2, is localized on chromosome band 9p21. CDKN2 is frequently deleted or mutated in a variety of tumor cell lines, including pancreatic cancer cell lines and xenografts, as well as in some primary tumors. We examined 32 primary pancreatic adenocarcinomas for CDKN2 mutations and for loss of heterozygosity of 9p21 sequences to assess the role of CDKN2 in pancreatic carcinogenesis. Single-strand conformation variant analysis (SSCV) and direct sequencing of the variants revealed somatic CDKN2 mutations in 11 of 32 tumors (five frame-shift mutations, five nonsense mutations, and one missense mutation). One tumor appeared to be characterized by homozygous deletion of CDKN2. These results suggest that CDKN2 plays an important role during tumorigenesis or tumor progression in a significant proportion of pancreatic adenocarcinomas.

摘要

编码细胞周期调节蛋白p16(即CDKN2)的基因定位于9号染色体的9p21带上。CDKN2在多种肿瘤细胞系中经常发生缺失或突变,包括胰腺癌细胞系和异种移植瘤,在一些原发性肿瘤中也是如此。我们检测了32例原发性胰腺腺癌的CDKN2突变情况以及9p21序列的杂合性缺失,以评估CDKN2在胰腺癌发生中的作用。单链构象变异分析(SSCV)及对变异体的直接测序显示,32例肿瘤中有11例存在体细胞CDKN2突变(5例移码突变、5例无义突变和1例错义突变)。1例肿瘤似乎以CDKN2纯合缺失为特征。这些结果表明,在相当一部分胰腺腺癌中,CDKN2在肿瘤发生或肿瘤进展过程中发挥着重要作用。

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