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烟草烟雾诱导的DNA损伤以及吸烟起始的早期年龄会导致肺癌中3p21处的染色体丢失。

Tobacco smoke-induced DNA damage and an early age of smoking initiation induce chromosome loss at 3p21 in lung cancer.

作者信息

Hirao T, Nelson H H, Ashok T D, Wain J C, Mark E J, Christiani D C, Wiencke J K, Kelsey K T

机构信息

Department of Cancer Cell Biology, Harvard School of Public Health, Boston, Massachusetts 02115-6021, USA.

出版信息

Cancer Res. 2001 Jan 15;61(2):612-5.

Abstract

The short arm of chromosome 3 is thought to harbor a novel oncogenic locus that is important in the genesis of lung cancer. The region at 3p21 is believed to contain a distinct locus that is sensitive to loss from the action of tobacco smoke carcinogens and has been reported to be specifically targeted for deletion in lung cancer. To investigate whether 3p21 alteration in lung cancer is associated with carcinogen exposure, PCR-based analysis was performed to detect loss of heterozygosity (LOH) on chromosome 3 at 3p21 in non-small cell lung carcinoma (NSCLC). We also measured instability at the BAT-26 locus, because the mismatch DNA repair gene, hMLH1, is found at 3p21. LOH at 3p21 was analyzed for association with the clinical features of NSCLC, p53 mutation status, polynuclear aromatic hydrocarbon-DNA adduct levels (measured using 32P-postlabeling) and carcinogen exposure information including cigarette smoking and asbestos exposure. Of 219 lung cancers, 150 cases (68.5%) were informative at the D3S1478 locus, and 44.2% of squamous cell carcinoma cases and 30.2% of adenocarcinoma cases showed 3p21 LOH. None of the cancers showed BAT-26 instability. The prevalence of 3p21 LOH was higher in both current and former smokers compared with never smokers and was higher in p53 mutated cases. Among squamous cell carcinoma cases, there was a strong association of increased 3p21 LOH with increasing polynuclear aromatic hydrocarbon-DNA adducts levels (P = 0.03), as well as an increased prevalence LOH with earlier age of smoking initiation (P = 0.02). Our results confirm that 3p21 LOH is strongly associated with measures of biologically effective dose of exposure to tobacco carcinogens. Our results also suggest that alterations of hMLH1 are not related to any of the reported associations, because there was no evidence of microsatellite instability. Finally, LOH in 3p21 may be an early molecular event in NSCLC, because it is significantly associated with a tendency to start smoking at a young age.

摘要

人们认为3号染色体的短臂包含一个新的致癌基因位点,它在肺癌发生过程中起重要作用。3p21区域被认为含有一个独特的位点,该位点对烟草烟雾致癌物作用导致的缺失敏感,并且据报道在肺癌中该区域是特异性缺失的靶点。为了研究肺癌中3p21改变是否与致癌物暴露相关,我们进行了基于聚合酶链反应(PCR)的分析,以检测非小细胞肺癌(NSCLC)中3p21处3号染色体上的杂合性缺失(LOH)。我们还检测了BAT - 26位点的不稳定性,因为错配DNA修复基因hMLH1位于3p21。分析3p21处的LOH与NSCLC临床特征、p53突变状态、多环芳烃 - DNA加合物水平(使用32P后标记法测量)以及包括吸烟和石棉暴露在内的致癌物暴露信息之间的关联。在219例肺癌中,150例(68.5%)在D3S1478位点具有信息性,44.2%的鳞状细胞癌病例和30.2%的腺癌病例显示3p21 LOH。所有癌症均未显示BAT - 26不稳定性。与从不吸烟者相比,当前吸烟者和既往吸烟者中3p21 LOH的发生率更高,且在p53突变病例中更高。在鳞状细胞癌病例中,3p21 LOH增加与多环芳烃 - DNA加合物水平升高(P = 0.03)以及随着开始吸烟年龄的提前LOH发生率增加(P = 0.02)之间存在强关联。我们的结果证实3p21 LOH与烟草致癌物暴露的生物学有效剂量测量值密切相关。我们的结果还表明,hMLH1的改变与任何已报道的关联均无关,因为没有微卫星不稳定性的证据。最后,3p21处的LOH可能是NSCLC中的一个早期分子事件,因为它与年轻时开始吸烟的倾向显著相关。

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