首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Formaldehyde-induced gene expression in F344 rat nasal respiratory epithelium.
【24h】

Formaldehyde-induced gene expression in F344 rat nasal respiratory epithelium.

机译:F344大鼠鼻呼吸道上皮中甲醛诱导的基因表达。

获取原文
获取原文并翻译 | 示例
           

摘要

Formaldehyde (FA), an occupational and environmental toxicant used extensively in the manufacturing of many household and personal use products, is known to induce squamous cell carcinomas in the nasal turbinates of rats and mice and squamous metaplasia in monkey noses. Tissue responses to FA include a dose dependent epithelial degeneration, respiratory cell hypertrophy, and squamous metaplasia. The primary target for FA-induced toxicity in both rodents and monkeys is the respiratory nasal epithelium. FA increases nasal epithelial cell proliferation and DNA-protein crosslinks (DPX) that are associated with subsequent nasal cancer development. To address the acute effects of FA exposure that might contribute to known pathological changes, cDNA gene expression analysis was used. Two groups of male F344 rats received either 40 ul of distilled water or FA (400 mM) instilled into each nostril. Twenty-four hours following treatment, nasal epithelium was recovered from which total RNA was used to generate cDNA probes. Significance analysis of microarrays (SAM) hybridization data using Clontech Rat Atlas 1.2 arrays revealed that 24 of the 1185 genes queried were significantly up-regulated and 22 genes were significantly downregulated. Results for ten of the differentially expressed genes were confirmed by quantitative real time RT PCR. The identified genes with FA-induced change in expression belong to the functional gene categories xenobiotic metabolism, cell cycle, apoptosis, and DNA repair. These data suggest that multiple pathways are dysregulated by FA exposure, including those involved in DNA synthesis/repair and regulation of cell proliferation. Differential gene expression profiles may provide clues that could be used to define mechanisms involved in FA-induced nasal cancer.
机译:甲醛(FA)是一种广泛用于制造许多家用和个人使用产品的职业和环境毒物,已知会在大鼠和小鼠的鼻甲和猴鼻的鳞状化生中诱发鳞状细胞癌。组织对FA的反应包括剂量依赖性上皮变性,呼吸细胞肥大和鳞状化生。 FA引起的啮齿动物和猴子毒性的主要目标是呼吸道鼻上皮。 FA会增加鼻上皮细胞的增殖和DNA-蛋白质交联(DPX),这些与随后的鼻癌发展有关。为了解决可能暴露于已知病理变化的FA暴露的急性影响,使用了cDNA基因表达分析。两组雄性F344大鼠接受40 ul蒸馏水或FA(400 mM)注入每个鼻孔。治疗后二十四小时,回收了鼻上皮,从中提取总RNA用于生成cDNA探针。使用Clontech Rat Atlas 1.2阵列进行的微阵列(SAM)杂交数据的意义分析表明,所查询的1185个基因中有24个显着上调,而22个基因则显着下调。通过定量实时RT PCR证实了十个差异表达基因的结果。鉴定出的具有FA诱导的表达变化的基因属于功能基因类别,异源生物代谢,细胞周期,细胞凋亡和DNA修复。这些数据表明,FA暴露会破坏多种途径,包括DNA合成/修复和细胞增殖调控的途径。差异基因表达谱可提供线索,可用于定义FA诱导的鼻癌所涉及的机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号