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首页> 外文期刊>Cell cycle >Delphinidin, a dietary anthocyanidin in pigmented fruits and vegetables: a new weapon to blunt prostate cancer growth.
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Delphinidin, a dietary anthocyanidin in pigmented fruits and vegetables: a new weapon to blunt prostate cancer growth.

机译:Delphinidin是一种有色水果和蔬菜中的饮食性花青素:一种抑制前列腺癌生长的新武器。

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In a recent publication, we have shown that delphinidin, an anthocyanidin induces apoptosis and cell cycle arrest in highly metastatic human prostate cancer (PCa) PC3 cells. Extending these studies, we provide additional evidence that delphinidin induces apoptosis and cell cycle arrest in androgen refractory human PCa 22Rnu1 cells and that these effects are concomitant with inhibition of NFkappaB. We observed that delphinidin treatment to 22Rnu1 cells resulted in a dose-dependent (i) G(2)/M phase cell cycle arrest, (ii) induction of apoptosis (iii) and inhibition of NFkappaB signaling. The induction of apoptosis by delphinidin was mediated via activation of caspases since a general caspase inhibitor Z-VAD-FMK significantly reversed this effect. Delphinidin treatment to cells resulted in a dose-dependent decrease in (i) phosphorylation of IKKgamma (NEMO), (ii) phosphorylation of NFkappaB inhibitory protein IkappaBalpha, (iii) phosphorylation of NFkappaB/p65 at Ser(536) and NFkappaB/p50 at Ser529, (iv) NFkappaB/p65 nuclear translocation, and (v) NFkappaB DNA binding activity. Taken together, our data show that delphinidin induces apoptosis of both androgen independent and androgen refractory human PCa cells via activation of caspases and in addition, this effect might be due to inhibition of NFkappaB signaling. We suggest that delphinidin could be developed as a novel agent against PCa.
机译:在最近的出版物中,我们显示了花青素delphinidin可以诱导高度转移性人前列腺癌(PCa)PC3细胞凋亡和细胞周期停滞。扩展这些研究,我们提供了额外的证据,飞燕草素可诱导雄激素难治性人PCa 22Rnu1细胞凋亡和细胞周期停滞,并且这些作用与NFkappaB的抑制作用同时发生。我们观察到对22Rnu1细胞的delphinidin治疗导致剂量依赖性(i)G(2)/ M期细胞周期停滞,(ii)诱导凋亡(iii)和抑制NFkappB信号传导。由于一般的半胱天冬酶抑制剂Z-VAD-FMK显着逆转了这种作用,因此由delphinidin诱导的凋亡是通过胱天蛋白酶的激活介导的。 Delphinidin对细胞的处理导致(i)IKKgamma(NEMO)的磷酸化,(ii)NFkappaB抑制蛋白IkappaBalpha的磷酸化,(iii)NFkappaB / p65在Ser(536)和NFkappaB / p50处的剂量依赖性降低Ser529,(iv)NFkappaB / p65核易位,和(v)NFkappaB DNA结合活性。两者合计,我们的数据表明,delphinidin通过胱天蛋白酶激活诱导雄激素非依赖性和雄激素难治性人类PCa细胞凋亡,此外,这种作用可能是由于NFkappaB信号传导的抑制。我们建议将delphinidin用作抗PCa的新型药物。

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