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首页> 外文期刊>Cell death & disease. >Inhibition of cancer progression by a novel trans -stilbene derivative through disruption of microtubule dynamics, driving G2/M arrest, and p53-dependent apoptosis
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Inhibition of cancer progression by a novel trans -stilbene derivative through disruption of microtubule dynamics, driving G2/M arrest, and p53-dependent apoptosis

机译:通过破坏微管动态,驱动G2 / M抑制和P53依赖性细胞凋亡,通过破坏新的反式苯丙甲衍生物抑制癌症进展。

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Resveratrol, a trans-stilbene polyphenolic compound and its synthetic analogs are widely used bioactive molecules due to their remarkable chemo-preventive potential. Here, we have identified a novel synthetic trans-stilbene compound, Z-DAN-11 ((Z)-3-(3, 4-dimethoxyphenyl)-2-(3, 4, 5-trimethoxyphenyl) acrylonitrile) which shows remarkable efficacy in blocking tumor growth and progression both in vitro and in vivo. Z-DAN-11 inhibits proliferation of cancer cells in vitro through microtubule depolymerization that induced G2/M arrest and consequently leads to apoptotic cell death. More importantly, Z-DAN-11 shows limited cytotoxicity to normal cells as compared to cancer cells. Quite interestingly, we have found that Z-DAN-11-mediated ROS production helps in dramatic alteration in the mitochondrial redox status which critically contributes to the apoptosis. Mechanistic studies reveal that Z-DAN-11 induces the expression of pro-apoptotic proteins and decreases anti-apoptotic protein expression that decisively helps in the activation of caspase 8, caspase 9, and caspase 3, leading to cleavage of PARP1 and cell death via intrinsic and extrinsic pathways of apoptosis. Moreover, Z-DAN-11-mediated apoptosis of cancer cells is through a partial p53-dependent pathway, since both HCT116 p53?/? cells as well as p53-silenced cells (siRNA) were able to block apoptosis partially but significantly. Importantly, Z-DAN-11 also imparts its anti-tumorigenic effect by inhibiting clonogenic property and anchorage-independent growth potential of cancer cells at concentrations at least 10 times lower than that required for inducing apoptosis. Finally, in vivo study with immuno-competent syngeneic mice shows Z-DAN-11 to be able to impede tumor progression without any adverse side-effects. Hence, we identified a novel, synthetic trans-stilbene derivative with anti-tumorigenic potential which might tremendously help in devising potential therapeutic strategy against cancer.
机译:由于其显着的化学预防潜力,白藜芦醇,一种反式甾醇的多酚化合物及其合成类似物是广泛使用的生物活性分子。在此,我们已经确定了一种新型合成反式甾醇化合物,Z-DAN-11((Z)-3-(3,4-二甲氧基苯基)-2-(3,4,5-三乙氧基苯基)丙烯腈,其显示出显着的功效在体外和体内阻断肿瘤生长和进展。 Z-DAN-11通过微管解聚的体外抑制癌细胞的增殖,诱导G2 / M被抑制,因此导致凋亡细胞死亡。更重要的是,与癌细胞相比,Z-DAN-11显示了与正常细胞的细胞毒性有限。非常有趣的是,我们发现Z-DAN-11介导的ROS生产有助于对线粒体氧化还原状态的显着改变,这对细胞凋亡有贡献。机械研究表明,Z-DAN-11诱导促凋亡蛋白的表达,降低抗凋亡蛋白表达,其果断地有助于Caspase 8,Caspase 9和Caspase 3的活化,导致PARP1和细胞死亡的裂解细胞凋亡的内在和外在途径。此外,Z-DAN-11介导的癌细胞的凋亡是通过部分P53依赖性途径,因为HCT116 P53?/?细胞以及P53-沉默的细胞(siRNA)能够部分地阻断细胞凋亡,但显着地阻断细胞凋亡。重要的是,Z-DAN-11还通过抑制浓度癌细胞的克隆因性和锚固无关的生长潜力来赋予抗致致致致致致致致致致致致致致致致致致致致致致致致致致荷的效果,其浓度比诱导细胞凋亡所需的至少10倍。最后,在体内与免疫主管同工小鼠的研究表明,Z-DAN-11能够阻碍肿瘤进展而没有任何不良副作用。因此,我们鉴定了一种具有抗旋转致瘤潜力的新型,合成的反式甾苯乙烯衍生物,这可能极大地有助于设计对癌症的潜在治疗策略。

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