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采用 A/J 小鼠验证主流香烟烟雾吸入诱导肺肿瘤发生模型。

Towards the validation of a lung tumorigenesis model with mainstream cigarette smoke inhalation using the A/J mouse.

机构信息

Philip Morris Research Laboratories GmbH, 51149 Cologne, Germany.

出版信息

Toxicology. 2013 Mar 8;305:49-64. doi: 10.1016/j.tox.2013.01.005. Epub 2013 Jan 24.

Abstract

A generally accepted and validated laboratory model for smoking-associated pulmonary tumorigenesis would be useful for both basic and applied research applications, such as the development of early diagnostic endpoints or the evaluation of modified risk tobacco products, respectively. The A/J mouse is susceptible for developing both spontaneous and induced lung adenomas and adenocarcinomas, and increased lung tumor multiplicities were also observed in previous cigarette smoke inhalation studies. The present study was designed to collect data useful towards the validation of an 18-month mainstream smoke (MS) inhalation model. Male and female A/J mice were exposed whole-body at three MS concentration levels for 6h/day, and the results were compared to a previous study in the same laboratory and with a similar design. A linear MS concentration-dependent increase in lung tumorigenesis was observed with similar slopes for both sexes and both studies and a maximal 5-fold increase in multiplicity beyond sham control. The minimal detectable difference in lung tumor multiplicity for the current study was 37%. In the larynx, papillomas were detectable in all MS-exposed groups in a non-concentration dependent manner. No other extra-pulmonary MS-dependent neoplastic lesions were found. Gene expression signatures of lung tumor tissues allowed a clear differentiation of sham- and high dose MS-exposed mice. In combination with data from previous smoke inhalation studies with A/J mice, the current data suggest that this model for MS inhalation-induced pulmonary tumorigenesis is reliable and relevant, two crucial requirements towards validation of such a model.

摘要

一个被广泛接受和验证的与吸烟相关的肺部肿瘤发生的实验室模型,将对基础和应用研究都很有用,例如开发早期诊断终点或评估改良风险烟草产品。A/J 小鼠易发生自发性和诱导性肺腺癌和肺腺癌,并且在以前的香烟烟雾吸入研究中也观察到肺肿瘤倍增数增加。本研究旨在收集有助于验证 18 个月主流烟雾(MS)吸入模型的数据。雄性和雌性 A/J 小鼠全身暴露于三种 MS 浓度水平下,每天 6 小时,并将结果与同一实验室的先前研究进行比较,设计类似。观察到 MS 浓度依赖性的肺肿瘤发生线性增加,两性和两项研究的斜率相似,多发性增加了 5 倍以上,超过了假对照。当前研究中肺肿瘤多发性的最小可检测差异为 37%。在喉中,所有 MS 暴露组中均可检测到乳头状瘤,无浓度依赖性。未发现其他肺外 MS 依赖性肿瘤病变。肺肿瘤组织的基因表达特征允许清晰地区分假对照和高剂量 MS 暴露的小鼠。结合 A/J 小鼠以前的烟雾吸入研究数据,当前数据表明,这种 MS 吸入诱导的肺部肿瘤发生模型是可靠和相关的,这是验证此类模型的两个关键要求。

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