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掌叶大黄粗提取物通过线粒体依赖性途径诱导U-2 OS人骨肉瘤细胞的细胞周期停滞于S期并诱导凋亡。

Crude extract of Rheum palmatum L. Induces cell cycle arrest S phase and apoptosis through mitochondrial-dependent pathways in U-2 OS human osteosarcoma cells.

作者信息

Lin Chin-Chung, Lee Ming-Huei, Lin Ju-Hwa, Lin Meng-Liang, Chueh Fu-Shin, Yu Chien-Chih, Lin Jing-Pin, Chou Yu-Cheng, Hsu Shu-Chun, Chung Jing-Gung

机构信息

Department of Chinese Medicine, Feng-Yuan Hospital, Ministry of Health and Welfare, Executive Yuan, Taichung, 420, Taiwan.

General Education Center, Central Taiwan University of Science and Technology, Taichung, 406, Taiwan.

出版信息

Environ Toxicol. 2016 Aug;31(8):957-69. doi: 10.1002/tox.22105. Epub 2015 Feb 17.

Abstract

Cancer is the second cause of death in children. Osteosarcoma is the most common primary malignancy of solid bone cancer primarily affecting adolescents and young adults. In the Chinese population, the crude extract of Rheum palmatum L. (CERP) has been used for treating different diseases, including SARS, rheumatoid arthritis, coxsackievirus B3, and human colon cancer cell, pancreatic cancer. There are no reports on CERP and human osteosarcoma cells. The present study examined effects of CERP on cytotoxicity including cell cycle distribution and cell death (apoptosis) in U-2 OS human osteosarcoma cells. CERP significantly induced S phase arrest in U-2 OS cells in a dose-dependent. CERP produced DNA damage and DNA condensation. Other effects of CERP were stimulation of ROS and Ca(2+) , mitochondria impairment, and activation of caspase-3, -8, and -9. CERP increased the levels of Bax, Bak, Bad, cyclin B, Fas, PARP, GRP78, GADD153, AIF, Endo G, Calpain-2, p21, and p27, but decreased the levels of Bcl-2, BCL-X, XIAP, Akt, CDC25A, CDK2, Cyclin A, and Cyclin E of U-2 OS cells. It was also observed that CERP promoted the expression of AIF, Endo G, GADD153, and cytochrome c. These results indicate that CERP has anticancer effects in vitro and provide the foundation for in vivo studies of animal models of osteosarcoma. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 957-969, 2016.

摘要

癌症是儿童死亡的第二大原因。骨肉瘤是实体骨癌中最常见的原发性恶性肿瘤,主要影响青少年和青年。在中国人群中,掌叶大黄粗提物(CERP)已被用于治疗多种疾病,包括非典、类风湿性关节炎、柯萨奇病毒B3以及人类结肠癌细胞、胰腺癌细胞。目前尚无关于CERP与人类骨肉瘤细胞的报道。本研究检测了CERP对U-2 OS人骨肉瘤细胞的细胞毒性作用,包括细胞周期分布和细胞死亡(凋亡)。CERP以剂量依赖性方式显著诱导U-2 OS细胞的S期阻滞。CERP导致DNA损伤和DNA凝聚。CERP的其他作用包括刺激活性氧和钙离子、线粒体损伤以及激活半胱天冬酶-3、-8和-9。CERP增加了U-2 OS细胞中Bax、Bak、Bad、细胞周期蛋白B、Fas、聚(ADP-核糖)聚合酶(PARP)、葡萄糖调节蛋白78(GRP78)、生长停滞和DNA损伤诱导蛋白153(GADD153)、凋亡诱导因子(AIF)、内切核酸酶G(Endo G)、钙蛋白酶-2、p21和p27的水平,但降低了Bcl-2、BCL-X、X连锁凋亡抑制蛋白(XIAP)、蛋白激酶B(Akt)、细胞周期蛋白依赖性激酶25A(CDC25A)、细胞周期蛋白依赖性激酶2(CDK2)、细胞周期蛋白A和细胞周期蛋白E的水平。还观察到CERP促进了AIF、Endo G、GADD153和细胞色素c的表达。这些结果表明CERP在体外具有抗癌作用,并为骨肉瘤动物模型的体内研究提供了基础。©2015威利期刊公司。《环境毒理学》31:957 - 969,2016年。

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