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后生动物种系基因中致癌突变变体的激活调查。

Survey for Activating Oncogenic Mutation Variants in Metazoan Germline Genes.

作者信息

Krueger Karl E

机构信息

National Cancer Institute, 9609 Medical Center Drive, 5E-132, Rockville, MD, 20850, USA.

出版信息

J Mol Evol. 2024 Dec;92(6):930-943. doi: 10.1007/s00239-024-10218-4. Epub 2024 Nov 26.

Abstract

Most cancers present with mutations or amplifications in distinctive tumor promoter genes that activate principal cell-signaling cascades promoting cell proliferation, dedifferentiation, cell survival, and replicative immortality. Somatic mutations found in this these driver proto-oncogenes invariably result in constitutive activation of the encoded protein. A salient feature of the activating mutations observed throughout many thousands of clinical tumor specimens reveals these driver missense mutations are recurrent and restricted to just one or very few codons of the entire gene, suggesting they have been positively selected during the course of tumor development. The purpose of this study is to investigate whether these characteristic oncogenic driver mutations are observed in the germline genes of any metazoan species. Six well-known tumor promoter genes were chosen for this survey including BRAF, KRAS, JAK2, PIK3CA, EGFR, and IDH1/2. The sites of all driver mutations were found to occur in highly conserved regions of each gene comparing protein sequences throughout diverse phyla of metazoan species. None of the oncogenic missense mutations were found in germlines of any species of current genome and protein databases. Despite many tumors readily selecting these somatic mutations, the conclusion drawn from this study is that these variants are negatively rejected if encountered as a germline mutation. While cancer expansion ensues from dysregulated growth elicited by these mutations, this effect is likely detrimental to embryonic development and/or survival of multicellular organisms. Although all oncogenic mutations considered here are gain-of-function where five of the six increase activity of the encoded proteins, clonal advancement promotes tumor growth by these genomic changes without conferring selection advantages benefiting the organism or species.

摘要

大多数癌症表现出独特的肿瘤启动子基因突变或扩增,这些基因激活主要的细胞信号级联反应,促进细胞增殖、去分化、细胞存活和复制永生。在这些驱动原癌基因中发现的体细胞突变总是导致编码蛋白的组成性激活。在数千份临床肿瘤标本中观察到的激活突变的一个显著特征是,这些驱动错义突变是反复出现的,并且仅限于整个基因的一个或极少数密码子,这表明它们在肿瘤发展过程中受到了正向选择。本研究的目的是调查在任何后生动物物种的种系基因中是否观察到这些特征性的致癌驱动突变。本调查选择了六个著名的肿瘤启动子基因,包括BRAF、KRAS、JAK2、PIK3CA、EGFR和IDH1/2。通过比较后生动物不同门类的蛋白质序列,发现所有驱动突变位点都发生在每个基因的高度保守区域。在当前的基因组和蛋白质数据库的任何物种的种系中都没有发现致癌错义突变。尽管许多肿瘤很容易选择这些体细胞突变,但本研究得出的结论是,如果这些变体作为种系突变出现,会被负面排斥。虽然这些突变引起的生长失调会导致癌症扩散,但这种效应可能对多细胞生物的胚胎发育和/或存活有害。尽管这里考虑的所有致癌突变都是功能获得性突变,六个中有五个增加了编码蛋白的活性,但克隆进展通过这些基因组变化促进肿瘤生长,而不会赋予有利于生物体或物种的选择优势。

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