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次氮基三乙酸铁诱导的肾细胞癌中ras突变缺失及p53突变低发生率

Absence of ras mutations and low incidence of p53 mutations in renal cell carcinomas induced by ferric nitrilotriacetate.

作者信息

Akiyama T, Hamazaki S, Okada S

机构信息

Department of Pathology, Okayama University Medical School.

出版信息

Jpn J Cancer Res. 1995 Dec;86(12):1143-9. doi: 10.1111/j.1349-7006.1995.tb03307.x.

Abstract

Renal cell carcinomas induced in male Wistar rats by iron chelate of nitrilotriacetate (Fe-NTA) were examined for mutations in ras oncogenes and p53 tumor suppressor gene. Fourteen primary tumors and two metastatic tumors from 11 animals were evaluated. Exons 1 and 2 of the H-, K-, and N-ras genes were amplified by polymerase chain reaction (PCR), and the presence of mutations was examined by direct sequencing. Exon 5 through exon 7 of p53 gene, including the 3' half of the conserved region II and the entire conserved region III through V, were surveyed for point mutations by PCR-single stranded conformation polymorphism (SSCP) analysis. Direct sequencing of the ras genes showed no mutations in codon 12, 13, or 61 among the tumors evaluated. SSCP analysis of p53 gene exon 6 indicated conformational changes in two primary tumors. One tumor had a CCG-to-CTG transition at codon 199, and the other had an ATC-to-att transition at codon 229 and two nonsense C-to-T transitions. These results suggest that neither ras genes nor p53 gene play a major role in the development of renal cell carcinomas induced by Fe-NTA.

摘要

对用次氮基三乙酸铁螯合物(Fe-NTA)诱导雄性Wistar大鼠产生的肾细胞癌进行了Ras癌基因和p53肿瘤抑制基因突变检测。评估了来自11只动物的14个原发性肿瘤和2个转移性肿瘤。通过聚合酶链反应(PCR)扩增H-Ras、K-Ras和N-Ras基因的第1和第2外显子,并通过直接测序检测是否存在突变。通过PCR-单链构象多态性(SSCP)分析对p53基因的第5外显子至第7外显子进行检测,包括保守区域II的3'端一半以及整个保守区域III至V,以寻找点突变。Ras基因的直接测序显示,在所评估的肿瘤中,密码子12、13或61未发生突变。p53基因第6外显子的SSCP分析表明,在两个原发性肿瘤中出现了构象变化。一个肿瘤在密码子199处发生了CCG到CTG的转变,另一个肿瘤在密码子229处发生了ATC到att的转变以及两个无义的C到T的转变。这些结果表明,Ras基因和p53基因在Fe-NTA诱导的肾细胞癌发生过程中均未发挥主要作用。

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1
Tandem double CC-->TT mutations are produced by reactive oxygen species.串联双CC→TT突变由活性氧产生。
Proc Natl Acad Sci U S A. 1993 May 1;90(9):3904-7. doi: 10.1073/pnas.90.9.3904.
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Structure of the rat p53 tumor suppressor gene.大鼠p53肿瘤抑制基因的结构
Nucleic Acids Res. 1993 Feb 11;21(3):713-7. doi: 10.1093/nar/21.3.713.
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The rat N-ras gene; interference of pseudogenes with the detection of activating point mutations.
Carcinogenesis. 1994 Feb;15(2):307-11. doi: 10.1093/carcin/15.2.307.

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