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在原发性、已切除的非小细胞肺癌中,p53基因的突变很常见。肺癌研究组。

Mutations in the p53 gene are frequent in primary, resected non-small cell lung cancer. Lung Cancer Study Group.

作者信息

Chiba I, Takahashi T, Nau M M, D'Amico D, Curiel D T, Mitsudomi T, Buchhagen D L, Carbone D, Piantadosi S, Koga H

机构信息

NCI-Navy Medical Oncology Branch, National Naval Medical Center, Bethesda, Maryland 20814.

出版信息

Oncogene. 1990 Oct;5(10):1603-10.

PMID:1979160
Abstract

The p53 gene has been implicated as a tumor suppressor gene with mutations found in common human cancers. We examined 51 early stage, primary, resected non-small cell lung cancer specimens using an RNAase protection assay and cDNA sequencing. Mutations changing the p53 coding sequence were found in 23/51 (45%) tumor specimens, but not in the corresponding normal lung, were distributed between codons 132 to 283, and included tumors with and without 17p allele loss. Fifteen of the 23 mutations lay in the predicted binding regions for SV40 large T antigen, and 14 were located in regions highly conserved between species. G to T transversions were a common result of p53 mutations in lung cancer compared to other cancers suggesting exposure to different mutagens. In univariate and multivariate analysis the presence of p53 mutations was associated with younger age and squamous histology. However, the presence of p53 mutations was not significantly associated with tumor stage, nodal status or sex and was found in all histologic types of lung cancer. We conclude that somatic mutations in the p53 gene play an important role in the pathogenesis of early stage non-small cell lung cancer.

摘要

p53基因被认为是一种肿瘤抑制基因,在常见人类癌症中发现有突变。我们使用核糖核酸酶保护分析法和cDNA测序对51份早期原发性非小细胞肺癌切除标本进行了检测。在23/51(45%)的肿瘤标本中发现了改变p53编码序列的突变,但在相应的正常肺组织中未发现,这些突变分布在密码子132至283之间,包括有和没有17p等位基因缺失的肿瘤。23个突变中有15个位于SV40大T抗原的预测结合区域,14个位于物种间高度保守的区域。与其他癌症相比,G到T颠换是肺癌中p53突变的常见结果,提示暴露于不同的诱变剂。在单因素和多因素分析中,p53突变的存在与年龄较轻和鳞状组织学相关。然而,p53突变的存在与肿瘤分期、淋巴结状态或性别无显著相关性,且在所有组织学类型的肺癌中均有发现。我们得出结论,p53基因的体细胞突变在早期非小细胞肺癌的发病机制中起重要作用。

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