首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Mutations in TP53 tumor suppressor gene in wood dust-related sinonasal cancer.
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Mutations in TP53 tumor suppressor gene in wood dust-related sinonasal cancer.

机译:木材粉尘相关鼻窦癌中TP53抑癌基因的突变。

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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.
机译:长期以来,通过大量的流行病学研究已经确定了与工作相关的木屑暴露在鼻窦癌发展中的因果作用。为了研究这些肿瘤中的分子变化,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例鼻息肉癌患者中TP53基因突变,无论有无职业接触木屑。观察到木屑暴露与腺癌组织学之间存在显着相关性[校正比值比(OR)12.6,95%置信区间(CI),5.0-31.6]。 TP53突变发生在所有组织中,总发生率为77%。 TP53突变阳性状态在腺癌中最常见(OR 2.0,95%CI,1.1-3.7;与鳞状细胞癌相比),突变阳性表明与木屑暴露总体无显着关联(OR 1.6,95%CI, 0.8-3.1)。 TP53突变的风险与持续时间(>或= 24年,OR 5.1,95%CI,1.5-17.1),平均水平(> 2 mg / m(3); OR 3.6,95%CI,1.2 -10.8)和累积水平(>或= 30 mg / m(3)x年;或3.5、95%CI,1.2-10.7);甲醛的调整仅轻微影响OR。吸烟并不影响TP53突变的发生。但是,它与多个突变相关(p = 0.03)。据我们所知,这是第一项通过职业暴露数据证明在大量鼻窦癌中TP53突变阳性病例高发的研究。我们的结果表明,突变机制,特别是TP53突变,与鼻窦癌中与工作相关的木屑接触有关。

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