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Cancer statistics, 2016.癌症统计数据,2016 年。
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Canine parvovirus NS1 induced apoptosis involves mitochondria, accumulation of reactive oxygen species and activation of caspases.犬细小病毒 NS1 诱导的细胞凋亡涉及线粒体、活性氧的积累和半胱天冬酶的激活。
Virus Res. 2016 Feb 2;213:46-61. doi: 10.1016/j.virusres.2015.10.019. Epub 2015 Nov 10.
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Twist-1 up-regulation in carcinoma correlates to poor survival.癌组织中Twist-1上调与生存率低相关。
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RNA interference: mechanisms, technical challenges, and therapeutic opportunities.RNA干扰:作用机制、技术挑战及治疗机遇
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Molecular mechanism of activating protein-4 regulated growth of hepatocellular carcinoma.活化蛋白-4调控肝细胞癌生长的分子机制
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Ilimaquinone induces death receptor expression and sensitizes human colon cancer cells to TRAIL-induced apoptosis through activation of ROS-ERK/p38 MAPK-CHOP signaling pathways.伊利马醌通过激活ROS-ERK/p38 MAPK-CHOP信号通路诱导死亡受体表达,并使人结肠癌细胞对TRAIL诱导的凋亡敏感。
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Repression of cyclin D1 expression is necessary for the maintenance of cell cycle exit in adult mammalian cardiomyocytes.细胞周期蛋白 D1 表达的抑制对于成年哺乳动物心肌细胞细胞周期退出的维持是必要的。
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AP‑4 predicts poor prognosis in non‑small cell lung cancer.AP-4预示非小细胞肺癌预后不良。
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Impact of high-fat feeding on basic helix-loop-helix transcription factors controlling enteroendocrine cell differentiation.高脂喂养对控制肠内分泌细胞分化的碱性螺旋-环-螺旋转录因子的影响。
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AP-4基因沉默可抑制人肺癌细胞增殖、诱导细胞周期停滞并促进其凋亡。

Silencing of AP-4 inhibits proliferation, induces cell cycle arrest and promotes apoptosis in human lung cancer cells.

作者信息

Hu Xuanyu, Guo Wei, Chen Shanshan, Xu Yizhuo, Li Ping, Wang Huaqi, Chu Heying, Li Juan, DU Yuwen, Chen Xiaonan, Zhang Guojun, Zhao Guoqiang

机构信息

Department of Microbiology and Immunology, College of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan 450001, P.R. China.

Department of Microbiology and Immunology, Henan Academy of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.

出版信息

Oncol Lett. 2016 Jun;11(6):3735-3742. doi: 10.3892/ol.2016.4451. Epub 2016 Apr 18.

DOI:10.3892/ol.2016.4451
PMID:27313685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4888253/
Abstract

Activating enhancer-binding protein (AP)-4 is a member of the basic helix-loop-helix transcription factors, and is involved in tumor biology. However, the role of AP-4 in human lung cancer remains to be fully elucidated. In the present study, the expression of AP-4 in human lung cancer tissues and cells was investigated by reverse transcription-quantitative polymerase chain reaction, and it was observed that the level of AP-4 was increased in tumor tissues and cells compared with their normal counterparts. AP-4 expression was knocked down by transfection with a specific small interfering RNA (siRNA) in lung cancer cells, and this indicated that siRNA-mediated silencing of AP-4 inhibited cell proliferation, arrested the cell cycle at the G0/G1 phase and induced apoptosis by modulating the expression of p21 and cyclin D1. The results of the present study suggest that AP-4 may be an oncoprotein that has a significant role in lung cancer, and that siRNA-mediated silencing of AP-4 may have therapeutic potential as a strategy for the treatment of lung cancer.

摘要

激活增强子结合蛋白(AP)-4是碱性螺旋-环-螺旋转录因子家族的成员,参与肿瘤生物学过程。然而,AP-4在人类肺癌中的作用仍有待充分阐明。在本研究中,通过逆转录-定量聚合酶链反应检测了AP-4在人肺癌组织和细胞中的表达,观察到与正常组织和细胞相比,肿瘤组织和细胞中AP-4的水平升高。通过转染特异性小干扰RNA(siRNA)敲低肺癌细胞中AP-4的表达,这表明siRNA介导的AP-4沉默通过调节p21和细胞周期蛋白D1的表达抑制细胞增殖,使细胞周期停滞在G0/G1期并诱导细胞凋亡。本研究结果表明,AP-4可能是一种在肺癌中起重要作用的癌蛋白,并且siRNA介导的AP-4沉默作为一种肺癌治疗策略可能具有治疗潜力。