癌变
克拉斯
癌症研究
肺癌
肿瘤发生
癌症
医学
肿瘤进展
信号转导
生物
病理
内科学
结直肠癌
遗传学
作者
Hironori Satoh,Takashi Moriguchi,Jun Takai,Masahito Ebina,Masayuki Yamamoto
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2013-04-23
卷期号:73 (13): 4158-4168
被引量:228
标识
DOI:10.1158/0008-5472.can-12-4499
摘要
Abstract Nrf2 (Nfe2l2) governs cellular defenses against oxidative and electrophilic stresses and protects against chemical carcinogenesis. However, many cancers have been found to accumulate NRF2 protein, raising questions of precisely how Nrf2 contributes to carcinogenesis. In this report, we explored such questions in an established urethane-induced multistep model of lung carcinogenesis. Consistent with earlier observations, Nrf2-deficient (Nrf2−/−) mice exhibited a relative increase in tumor foci by 8 weeks after urethane administration. However, after 16 weeks, we observed a relative reduction in the number of tumors with more malignant characteristics in Nrf2−/− mice. Furthermore, all Nrf2+/+ tumors harbored activated mutations in Kras, whereas Nrf2−/− tumors were rarely associated with similar Kras mutations. Overall, our results established that Nrf2 has two roles during carcinogenesis, one of which is preventive during tumor initiation and the second that promotes malignant progression. These findings establish Nrf2 inhibitors as rational tools to prevent malignant progression in lung cancer, whereas Nrf2 activators are more suited for lung cancer prevention. Cancer Res; 73(13); 4158–68. ©2013 AACR.
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