O-Wang J, Kawamura K, Tada Y, Ohmori H, Kimura H, Sakiyama S, Tagawa M
Division of Pathology, Chiba Cancer Center Research Institute, Chiba 260-8717, Japan.
Cancer Res. 2001 Jul 15;61(14):5366-9.
DNA polymerase kappa (Pol kappa) is a newly identified low-fidelity polymerase implicated in spontaneous and DNA damage-induced mutagenesis. As an initial study to investigate its possible involvement in tumorigenesis, we compared the expression level of Pol kappa in tumors and adjacent nontumorous tissues by Northern blot, semiquantitative RT-PCR, and Western blot analyses. In this study, paired tumor and normal specimens from 29 patients with stages I to IIIb non-small cell lung cancer (NSCLC), including 13 adenocarcinomas, 15 squamous cell cancers, and 1 adenosquamous carcinoma, were analyzed, among which different levels of tumor-associated Pol kappa overexpression were observed in 21 of 29 matched specimens. In addition, five matched specimens exhibited elevated Pol kappa expression in both tumor and control tissues, whereas only one nontumorous tissue expressed a higher level of Pol kappa than its tumor counterpart. The preferential up-regulation of Pol kappa expression in tumors was highly significant (P < 0.001). There was no apparent correlation of Pol kappa expression levels with tumor histology, grade, and stage or with smoking history. Southern blot analysis did not show amplification of the Pol kappa gene, indicating that the elevated Pol kappa expression is likely attributable to dysregulated transcription. Our data suggest that Pol kappa may contribute to lung tumor development by accelerating the accumulation of mutations.
DNA聚合酶κ(Pol κ)是一种新发现的低保真度聚合酶,与自发突变和DNA损伤诱导的诱变有关。作为研究其可能参与肿瘤发生的初步研究,我们通过Northern印迹、半定量RT-PCR和Western印迹分析比较了肿瘤组织和相邻非肿瘤组织中Pol κ的表达水平。在本研究中,分析了29例I至IIIb期非小细胞肺癌(NSCLC)患者的配对肿瘤和正常标本,其中包括13例腺癌、15例鳞状细胞癌和1例腺鳞癌,在29对匹配标本中的21对中观察到不同水平的与肿瘤相关的Pol κ过表达。此外,5对匹配标本在肿瘤组织和对照组织中均表现出Pol κ表达升高,而只有1例非肿瘤组织表达的Pol κ水平高于其对应的肿瘤组织。肿瘤中Pol κ表达的优先上调非常显著(P < 0.001)。Pol κ表达水平与肿瘤组织学、分级、分期或吸烟史无明显相关性。Southern印迹分析未显示Pol κ基因的扩增,表明Pol κ表达升高可能归因于转录失调。我们的数据表明,Pol κ可能通过加速突变积累促进肺肿瘤发展。