Pan Li, Peng Xing-Chen, Yuan Qing-Zhong, Leng Fei, Yu Dan-Dan, Shan Yan, Li Zhi-Yong, Wang Chun-Ting
State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2010 May;41(3):390-3.
To investigate the effect of Survivin-T34A mutant on murine prostate cancer and its apoptosis-inducing efficacy in vivo and in vitro.
In vitro, prostate cancer cells TRAMP-C1 were transfected with Survivin-T34A plasmid encapsulated by cationic liposome. The apoptosis of TRAMP-C1 was evaluated with flow cytometry. C57BL/6 mice model with TRAMP-C1 prostate cancer was established. Twenty four male mice with TRAMP-C1 prostate cancers were divided randomly into three groups, which were intravenously injected with normal saline, empty vector PORF-9-null encapsulated by cationic liposome and Survivin-T34A plasmid encapsulated by cationic liposome respectively twice a week for eight doses. The size of tumors was measured and the tumor sections of each group were stained with TUNEL reagent for apoptosis detection.
An apoptotic index of 46% of TRAMP-C1 transfected with Survivin-T34A plasmid encapsulated by cationic liposome was observed. The tumor volume of Survivin-T34A group of C57BL/6 mice with TRAMP-C1 prostate cancer was far smaller than those in the control groups (P < 0.05) and the tumors treated with Survivin-T34A showed significant increase of apoptosis compared with those of control groups (P < 0.05).
Survivin-T34A mutant efficiently inhibits the growth of prostate cancer, which is based on the mechanism of Survivin-T34A mutant inducing apoptosis of tumor cells.
研究Survivin-T34A突变体对小鼠前列腺癌的影响及其体内外诱导凋亡的效果。
体外实验中,用阳离子脂质体包裹的Survivin-T34A质粒转染前列腺癌细胞TRAMP-C1。采用流式细胞术评估TRAMP-C1的凋亡情况。建立TRAMP-C1前列腺癌的C57BL/6小鼠模型。将24只患有TRAMP-C1前列腺癌的雄性小鼠随机分为三组,分别每周静脉注射两次生理盐水、阳离子脂质体包裹的空载体PORF-9-null和阳离子脂质体包裹的Survivin-T34A质粒,共注射八次。测量肿瘤大小,每组肿瘤切片用TUNEL试剂染色以检测凋亡情况。
观察到用阳离子脂质体包裹的Survivin-T34A质粒转染的TRAMP-C1的凋亡指数为46%。TRAMP-C1前列腺癌的C57BL/6小鼠Survivin-T34A组的肿瘤体积远小于对照组(P<0.05),且与对照组相比,用Survivin-T34A治疗的肿瘤凋亡显著增加(P<0.05)。
Survivin-T34A突变体通过诱导肿瘤细胞凋亡的机制有效抑制前列腺癌的生长。