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TP53 抑癌基因在木尘相关鼻窦癌中的突变。

Mutations in TP53 tumor suppressor gene in wood dust-related sinonasal cancer.

机构信息

Finnish Institute of Occupational Health, Helsinki, Finland.

出版信息

Int J Cancer. 2010 Aug 1;127(3):578-88. doi: 10.1002/ijc.25064.

Abstract

The causal role of work-related exposure to wood dust in the development of sinonasal cancer has long been established by numerous epidemiologic studies. To study molecular changes in these tumors, we analyzed TP53 gene mutations in 358 sinonasal cancer cases with or without occupational exposure to wood dust, using capillary electrophoresis single-strand conformation polymorphism analysis and direct sequencing. A significant association between wood-dust exposure and adenocarcinoma histology was observed [adjusted odds ratio (OR) 12.6, 95% confidence interval (CI), 5.0-31.6]. TP53 mutations occurred in all histologies, with an overall frequency of 77%. TP53 mutation positive status was most common in adenocarcinoma (OR 2.0, 95% CI, 1.1-3.7; compared with squamous cell carcinoma), and mutation positivity showed an overall, nonsignificant association with wood-dust exposure (OR 1.6, 95% CI, 0.8-3.1). Risk of TP53 mutation was significantly increased in association with duration (> or =24 years, OR 5.1, 95% CI, 1.5-17.1), average level (>2 mg/m(3); OR 3.6, 95% CI, 1.2-10.8) and cumulative level (> or =30 mg/m(3) x years; OR 3.5, 95% CI, 1.2-10.7) of wood-dust exposure; adjustment for formaldehyde affected the ORs only slightly. Smoking did not influence the occurrence of TP53 mutation; however, it was associated with multiple mutations (p = 0.03). As far as we are aware, this is the first study to demonstrate a high prevalence of TP53 mutation-positive cases in a large collection of sinonasal cancers with data on occupational exposure. Our results indicate that mutational mechanisms, in particular TP53 mutations, are associated with work-related exposure to wood dust in sinonasal cancer.

摘要

工作中接触木尘与鼻窦癌发生之间的因果关系早已被大量的流行病学研究所证实。为了研究这些肿瘤的分子变化,我们使用毛细管电泳单链构象多态性分析和直接测序分析了 358 例鼻窦癌病例中与职业性接触木尘有关的 TP53 基因突变。我们发现木尘暴露与腺癌组织学之间存在显著关联[调整后的比值比(OR)为 12.6,95%置信区间(CI)为 5.0-31.6]。TP53 突变发生于所有组织学类型,总体发生率为 77%。TP53 突变阳性状态在腺癌中最为常见(OR 2.0,95%CI,1.1-3.7;与鳞状细胞癌相比),并且突变阳性与木尘暴露之间存在总体上无统计学意义的关联(OR 1.6,95%CI,0.8-3.1)。TP53 突变的风险与暴露时间(≥24 年,OR 5.1,95%CI,1.5-17.1)、暴露平均水平(>2mg/m(3);OR 3.6,95%CI,1.2-10.8)和累积水平(>或=30mg/m(3)x 年;OR 3.5,95%CI,1.2-10.7)呈显著正相关;调整甲醛因素后 OR 值仅有轻微变化。吸烟对 TP53 突变的发生没有影响;但是,它与多个突变有关(p=0.03)。据我们所知,这是第一项研究表明,在有职业性接触木尘数据的大型鼻窦癌病例集中,TP53 突变阳性病例的比例很高。我们的研究结果表明,在鼻窦癌中,突变机制,特别是 TP53 突变,与工作相关的木尘暴露有关。

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