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p53基因密码子72多态性与晚期肺癌的关联:精氨酸(Arg)等位基因在精氨酸/脯氨酸(Arg/Pro)种系杂合子产生的肿瘤中优先保留。

Association of p53 codon 72 polymorphism with advanced lung cancer: the Arg allele is preferentially retained in tumours arising in Arg/Pro germline heterozygotes.

作者信息

Papadakis E D, Soulitzis N, Spandidos D A

机构信息

Laboratory of Virology, Medical School, University of Crete, PO Box 1393, Heraklion, Crete, Greece.

出版信息

Br J Cancer. 2002 Oct 21;87(9):1013-8. doi: 10.1038/sj.bjc.6600595.

DOI:10.1038/sj.bjc.6600595
PMID:12434294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2364333/
Abstract

The association of p53 codon 72 polymorphism with cancer has been investigated by several scientific groups with controversial results. In the present study, we examined the genotypic frequency of this polymorphism in 54 patients with advanced lung cancer and 99 normal controls from the geographical region of Greece. Sputum and bronchial washing samples from each patient were assayed for the presence of human papillomavirus. Codon 72 heterozygous (Arg/Pro) patients were also analysed for loss of heterozygosity at the TP53 locus, in order to determine the lost p53 allele (Arg or Pro). p53 Arg/Arg genotype was significantly increased in lung cancer patients compared to normal controls (50% vs 24.2%, P<0.002). Human papillomavirus was detected only in two patients (3.7%). Loss of heterozygosity at the TP53 locus was found in 14 out of 27 Arg/Pro patients (51.85%). The Pro allele was lost in 11 cases (78.6%), while the Arg allele was lost in three (21.4%). Our results suggest that p53 codon 72 Arg homozygosity is associated with advanced lung cancer, and that the Arg allele is preferentially retained in patients heterozygous for this polymorphism. On the other hand, human papillomavirus infection does not seem to play an important role in lung carcinogenesis.

摘要

几个科研团队对p53密码子72多态性与癌症的关联进行了研究,结果存在争议。在本研究中,我们检测了希腊地区54例晚期肺癌患者和99例正常对照者中该多态性的基因型频率。检测了每位患者的痰液和支气管冲洗样本中是否存在人乳头瘤病毒。还对密码子72杂合(Arg/Pro)患者的TP53基因座杂合性缺失进行了分析,以确定缺失的p53等位基因(Arg或Pro)。与正常对照相比,肺癌患者中p53 Arg/Arg基因型显著增加(50%对24.2%,P<0.002)。仅在两名患者(3.7%)中检测到人乳头瘤病毒。在27例Arg/Pro患者中有14例(51.85%)发现TP53基因座杂合性缺失。Pro等位基因在11例(78.6%)中缺失,而Arg等位基因在3例(21.4%)中缺失。我们的结果表明,p53密码子72的Arg纯合性与晚期肺癌相关,并且在该多态性的杂合患者中Arg等位基因优先保留。另一方面,人乳头瘤病毒感染似乎在肺癌发生中不起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810b/2364333/cc4ed634d5b0/87-6600595f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810b/2364333/1e03fb76c242/87-6600595f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810b/2364333/cc4ed634d5b0/87-6600595f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810b/2364333/1e03fb76c242/87-6600595f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/810b/2364333/cc4ed634d5b0/87-6600595f2.jpg

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P53 codon 72 polymorphism in bladder cancer--no evidence of association with increased risk or invasiveness.膀胱癌中P53密码子72多态性——无证据表明与风险增加或侵袭性有关。
Single nucleotide variants in lung cancer.
肺癌中的单核苷酸变异
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Cancers (Basel). 2023 Sep 27;15(19):4747. doi: 10.3390/cancers15194747.
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