Wei Ming-Ming, Zhou Yong-Chun, Wen Zhe-Sheng, Zhou Bo, Huang Yun-Chao, Wang Gui-Zhen, Zhao Xin-Chun, Pan Hong-Li, Qu Li-Wei, Zhang Jian, Zhang Chen, Cheng Xin, Zhou Guang-Biao
State Key Laboratory of Membrane Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Department of Thoracic Surgery, The Third Affiliated Hospital of Kunming Medical University (Yunnan Tumor Hospital), Kunming 650106, China.
Oncotarget. 2016 Sep 13;7(37):59556-59571. doi: 10.18632/oncotarget.10006.
Indoor and outdoor air pollution has been classified as group I carcinogen in humans, but the underlying tumorigenesis remains unclear. Here, we screened for abnormal long noncoding RNAs (lncRNAs) in lung cancers from patients living in Xuanwei city which has the highest lung cancer incidence in China due to smoky coal combustion-generated air pollution. We reported that Xuanwei patients had much more dysregulated lncRNAs than patients from control regions where smoky coal was not used. The lncRNA CAR intergenic 10 (CAR10) was up-regulated in 39/62 (62.9%) of the Xuanwei patients, which was much higher than in patients from control regions (32/86, 37.2%; p=0.002). A multivariate regression analysis showed an association between CAR10 overexpression and air pollution, and a smoky coal combustion-generated carcinogen dibenz[a,h]anthracene up-regulated CAR10 by increasing transcription factor FoxF2 expression. CAR10 bound and stabilized transcription factor Y-box-binding protein 1 (YB-1), leading to up-regulation of the epidermal growth factor receptor (EGFR) and proliferation of lung cancer cells. Knockdown of CAR10 inhibited cell growth in vitro and tumor growth in vivo. These results demonstrate the role of lncRNAs in environmental lung carcinogenesis, and CAR10-YB-1 represents a potential therapeutic target.
室内和室外空气污染已被归类为人类I类致癌物,但其潜在的肿瘤发生机制仍不清楚。在此,我们对居住在中国肺癌发病率最高的宣威市的肺癌患者中的异常长链非编码RNA(lncRNA)进行了筛查,该市因燃烧烟煤产生的空气污染导致肺癌高发。我们报告称,与未使用烟煤的对照地区的患者相比,宣威患者中失调的lncRNA要多得多。长链非编码RNA CAR基因间区10(CAR10)在39/62(62.9%)的宣威患者中上调,这一比例远高于对照地区的患者(32/86,37.2%;p=0.002)。多变量回归分析显示CAR10过表达与空气污染之间存在关联,燃烧烟煤产生的致癌物二苯并[a,h]蒽通过增加转录因子FoxF2的表达上调CAR10。CAR10结合并稳定转录因子Y盒结合蛋白1(YB-1),导致表皮生长因子受体(EGFR)上调和肺癌细胞增殖。敲低CAR10可抑制体外细胞生长和体内肿瘤生长。这些结果证明了lncRNA在环境性肺癌发生中的作用,并且CAR10-YB-1代表了一个潜在的治疗靶点。