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葡萄籽提取物诱导人前列腺癌LNCaP细胞发生失巢凋亡和半胱天冬酶介导的凋亡:共济失调毛细血管扩张突变型p53激活的可能作用

Grape seed extract induces anoikis and caspase-mediated apoptosis in human prostate carcinoma LNCaP cells: possible role of ataxia telangiectasia mutated-p53 activation.

作者信息

Kaur Manjinder, Agarwal Rajesh, Agarwal Chapla

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, University of Colorado Health Sciences Center, 4200 East Ninth Avenue, Box C238, Denver, CO 80262.

出版信息

Mol Cancer Ther. 2006 May;5(5):1265-74. doi: 10.1158/1535-7163.MCT-06-0014.

Abstract

Prostate cancer is the second leading cancer diagnosed in elderly males in the Western world. Epidemiologic studies suggest that dietary modifications could be an effective approach in reducing various cancers, including prostate cancer, and accordingly cancer-preventive efficacy of dietary nutrients has gained increased attention in recent years. We have recently shown that grape seed extract (GSE) inhibits growth and induces apoptotic death of advanced human prostate cancer DU145 cells in culture and xenograft. Because prostate cancer is initially an androgen-dependent malignancy, here we used LNCaP human prostate cancer cells as a model to assess GSE efficacy and associated mechanisms. GSE treatment of cells led to their detachment within 12 hours, as occurs in anoikis, and caused a significant decrease in live cells mostly due to their apoptotic death. GSE-induced anoikis and apoptosis were accompanied by a strong decrease in focal adhesion kinase levels, but an increase in caspase-3, caspase-9, and poly(ADP-ribose) polymerase cleavage; however, GSE caused both caspase-dependent and caspase-independent apoptosis as evidenced by cytochrome c and apoptosis-inducing factor release into cytosol. Additional studies revealed that GSE causes DNA damage-induced activation of ataxia telangiectasia mutated kinase and Chk2, as well as p53 Ser(15) phosphorylation and its translocation to mitochondria, suggesting this to be an additional mechanism for apoptosis induction. GSE-induced apoptosis, cell growth inhibition, and cell death were attenuated by pretreatment with N-acetylcysteine and involved reactive oxygen species generation. Together, these results show GSE effects in LNCaP cells and suggest additional in vivo efficacy studies in prostate cancer animal models.

摘要

前列腺癌是西方世界老年男性中第二大常见癌症。流行病学研究表明,饮食调整可能是降低包括前列腺癌在内的各种癌症的有效方法,因此饮食营养成分的防癌功效近年来受到了更多关注。我们最近发现,葡萄籽提取物(GSE)在体外培养和异种移植中可抑制晚期人类前列腺癌DU145细胞的生长并诱导其凋亡死亡。由于前列腺癌最初是雄激素依赖性恶性肿瘤,因此我们在此使用LNCaP人前列腺癌细胞作为模型来评估GSE的功效及相关机制。用GSE处理细胞会导致它们在12小时内脱离,如同失巢凋亡发生时那样,并且导致活细胞显著减少,这主要是由于其凋亡死亡。GSE诱导的失巢凋亡和凋亡伴随着粘着斑激酶水平的大幅下降,但半胱天冬酶-3、半胱天冬酶-9和聚(ADP-核糖)聚合酶的裂解增加;然而,GSE导致了半胱天冬酶依赖性和半胱天冬酶非依赖性凋亡,这可通过细胞色素c和凋亡诱导因子释放到细胞质中得到证明。进一步的研究表明,GSE会导致DNA损伤诱导的共济失调毛细血管扩张突变激酶和Chk2的激活,以及p53丝氨酸(15)磷酸化及其向线粒体的转位,这表明这是诱导凋亡的另一种机制。用N-乙酰半胱氨酸预处理可减弱GSE诱导的凋亡、细胞生长抑制和细胞死亡,且这涉及活性氧的产生。总之,这些结果显示了GSE对LNCaP细胞的作用,并提示在前列腺癌动物模型中进行更多的体内功效研究。

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