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首页> 外文期刊>Molecular and Cellular Biochemistry >Effects of diallyl disulfide (DADS) on expression of apoptosis associated proteins in androgen independent human prostate cancer cells (PC-3)
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Effects of diallyl disulfide (DADS) on expression of apoptosis associated proteins in androgen independent human prostate cancer cells (PC-3)

机译:二烯丙基二硫(DADS)对雄激素非依赖性人前列腺癌细胞(PC-3)中凋亡相关蛋白表达的影响

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Prostate cancer is a leading cause of death among the aging men. Surgical or radiotherapy is effective when the cancer is confined to the prostate gland but once the cancer spreads beyond the pelvis even chemotherapy and hormonal ablation therapy fails in curing this disease. Our previous studies have shown that diallyl disulfide (DADS) induces cell cycle arrest and also induces apoptosis in PC-3 cells. And now the present study is focused to see whether there is an activation of caspase cascade pathway. Hence, in the present study the apoptotic effect of DADS is studied by Western blot analysis of caspase-3, -9, -10 and Bcl-2, Bad, and Bax protein. The Apoptotic cells were assessed by Hoechst 33342 staining with 25 and 40 μM concentrations of DADS for 24 h. The results have shown that DADS at 25 and 40 μM concentrations has induced the activation of caspases. There is a significant increase in the expression of caspases (3, 9, and 10). The proapoptotic protein Bax has significantly increased at 40 μM of DADS treatment and there is significant increase of Bad protein at both the concentration. Bcl-2 protein has significantly decreased in DADS treated cells. Therefore, the present investigation serves as evidence that DADS may be a therapeutic drug in the treatment of prostate cancer.
机译:前列腺癌是衰老男性死亡的主要原因。当癌症仅限于前列腺时,手术或放射疗法是有效的,但是一旦癌症扩散到骨盆之外,则即使化学疗法和激素消融疗法也无法治愈该疾病。我们以前的研究表明,二烯丙基二硫化物(DADS)诱导细胞周期停滞,并诱导PC-3细胞凋亡。现在,本研究着眼于是否存在胱天蛋白酶级联途径的激活。因此,在本研究中,通过对caspase-3,-9,-10和Bcl-2,Bad和Bax蛋白的蛋白质印迹分析来研究DADS的凋亡作用。通过用25和40μM浓度的DADS进行24小时的Hoechst 33342染色来评估凋亡细胞。结果表明,浓度为25和40μM的DADS诱导了胱天蛋白酶的激活。半胱天冬酶的表达显着增加(3、9和10)。在40μM的DADS处理中,促凋亡蛋白Bax显着增加,并且在两种浓度下Bad蛋白均显着增加。在DADS处理的细胞中,Bcl-2蛋白显着降低。因此,本研究作为证据证明DADS可以是治疗前列腺癌的治疗药物。

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