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转谷氨酰胺酶2参与缺氧条件下骨肉瘤细胞系U2OS的细胞凋亡。

Transglutaminase-2 is Involved in Cell Apoptosis of Osteosarcoma Cell Line U2OS Under Hypoxia Condition.

作者信息

Wang Wei, Li Xiao, Han Xiang-Zhen, Meng Fan-Bin, Wang Zhen-Xing, Zhai Yong-Qing, Zhou Dong-Sheng

机构信息

Department of Orthopedics, Linyi People's Hospital Affiliated to Shandong University, Linyi, 276000, Shandong, People's Republic of China.

Department of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, 324 Jing-Wu Road, Jinan, 250021, Shandong, People's Republic of China.

出版信息

Cell Biochem Biophys. 2015 May;72(1):283-8. doi: 10.1007/s12013-014-0451-1.

Abstract

Osteosarcoma is the most common type of solid bone cancer, which is the second leading cause of cancer-related death. Hypoxia is an ordinary phenomenon in solid tumor tissues and can induce cell apoptosis but the specific molecular mechanism remains unclear. In this study, we explored the effect and the molecular mechanism of Transglutaminase 2 (TG2) on cell apoptosis in osteosarcoma U2OS cells under hypoxia. We found the enzymatic activity of TG2 is significantly increased and the expression of TG2 is remarkably up-regulated under hypoxia condition. Cell apoptotic rate is markedly increased upon knockdown of TG2 by siRNA under hypoxia. We further investigated the mechanism of cell apoptosis and found Bax protein is significantly increased after depletion of TG2 under hypoxia. Moreover, our data also show that cytochrome C (Cyt C) is significantly increased in cytoplasm and markedly decreased in mitochondria of U2OS cells after depletion of TG2 under hypoxia. Our results suggest that TG2 can inhibit tumor cell apoptosis through down-regulation of Bax and prevention of release Cyt C from mitochondria into cytoplasm.

摘要

骨肉瘤是最常见的实体骨癌类型,是癌症相关死亡的第二大主要原因。缺氧是实体瘤组织中的常见现象,可诱导细胞凋亡,但其具体分子机制仍不清楚。在本研究中,我们探讨了转谷氨酰胺酶2(TG2)在缺氧条件下对骨肉瘤U2OS细胞凋亡的影响及其分子机制。我们发现缺氧条件下TG2的酶活性显著增加,TG2的表达明显上调。缺氧条件下,通过siRNA敲低TG2后,细胞凋亡率显著增加。我们进一步研究了细胞凋亡机制,发现缺氧条件下TG2缺失后Bax蛋白显著增加。此外,我们的数据还表明,缺氧条件下TG2缺失后,U2OS细胞胞质中的细胞色素C(Cyt C)显著增加,线粒体中的细胞色素C显著减少。我们的结果表明,TG2可通过下调Bax和阻止Cyt C从线粒体释放到细胞质中来抑制肿瘤细胞凋亡。

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