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氨基甲酸乙酯诱导的小鼠肺腺瘤中连接蛋白的表达改变。

Altered expression of connexins in urethane-induced mouse lung adenomas.

作者信息

Avanzo José Luis, Mesnil Marc, Hernandez-Blazquez Francisco Javier, da Silva Tereza Cristina, Fukumasu Heidge, Mori Claudia Madalena Cabrera, Yamasaki Hiroshi, Dagli Maria Lúcia Zaidan

机构信息

Laboratory of Experimental Oncology, Department of Pathology, Faculty of Veterinary Medicine and Animal Science, University of São Paulo, Brazil.

出版信息

Life Sci. 2006 Nov 2;79(23):2202-8. doi: 10.1016/j.lfs.2006.07.033. Epub 2006 Aug 3.

Abstract

Lung carcinogenesis is a multistep process whose molecular alterations can be studied in mouse models. Urethane, a specific lung tumor carcinogen, can induce adenomas in mice. Mouse lung alveolar cells reportedly generate lung neoplasms, and express connexins 26, 32, 43 and 46. The aim of the present study was to evaluate the expression of connexins in urethane-induced lung adenomas. Fifteen-day-old CD1 male mice received 2 i.p. injections of urethane (1.5 g/kg bw). The mice were euthanized 25 weeks after urethane injection, and lung adenomas were quantified. Lung tissue and lung adenomas were harvested and the RNA was extracted. The expression of connexins 26, 32, 43 and 46 was evaluated by Real-Time PCR, and these proteins were identified by Western blot. Immunohistochemistry revealed the distribution pattern of these connexins in lung tissue and adenomas. The treatment with urethane was associated with the downregulation of Cx26, 32 and 46 expressions, and with the upregulation of Cx43 expression in lung tissue. Surprisingly, in lung adenomas Cx32 and Cx43 expressions were not detected, although the expression of connexins 26 and 46 was present. Western blot and immunohistochemistry corroborated the RT-PCR data. These results may indicate a role of Cx32 and Cx43 in urethane-induced lung carcinogenesis, since their absence may contribute to the development of urethane induced lung tumors. The role of Cx26 and Cx46 is yet to be determined.

摘要

肺癌发生是一个多步骤过程,其分子改变可在小鼠模型中进行研究。氨基甲酸乙酯是一种特定的肺肿瘤致癌物,可在小鼠中诱导腺瘤形成。据报道,小鼠肺泡细胞可产生肺部肿瘤,并表达连接蛋白26、32、43和46。本研究的目的是评估连接蛋白在氨基甲酸乙酯诱导的肺腺瘤中的表达。15日龄的CD1雄性小鼠腹腔注射2次氨基甲酸乙酯(1.5 g/kg体重)。在注射氨基甲酸乙酯25周后对小鼠实施安乐死,并对肺腺瘤进行定量分析。采集肺组织和肺腺瘤并提取RNA。通过实时定量PCR评估连接蛋白26、32、43和46的表达,并通过蛋白质印迹法鉴定这些蛋白。免疫组织化学揭示了这些连接蛋白在肺组织和腺瘤中的分布模式。氨基甲酸乙酯处理与肺组织中Cx26、32和46表达的下调以及Cx43表达的上调相关。令人惊讶的是,在肺腺瘤中未检测到Cx32和Cx43的表达,尽管存在连接蛋白26和46的表达。蛋白质印迹法和免疫组织化学证实了实时定量PCR数据。这些结果可能表明Cx32和Cx43在氨基甲酸乙酯诱导的肺癌发生中起作用,因为它们的缺失可能有助于氨基甲酸乙酯诱导的肺肿瘤的发展。Cx26和Cx46的作用尚待确定。

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