首页> 外文期刊>International journal of gynecological cancer: official journal of the International Gynecological Cancer Society >Effects and mechanisms of anti-CD44 monoclonal antibody A3D8 on proliferation and apoptosis of sphere-forming cells with stemness from human ovarian cancer
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Effects and mechanisms of anti-CD44 monoclonal antibody A3D8 on proliferation and apoptosis of sphere-forming cells with stemness from human ovarian cancer

机译:抗CD44单克隆抗体A3D8对人卵巢癌干球形成细胞增殖和凋亡的影响及其机制

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Objective: CD44+ human ovarian cancer stem cells (CSCs) and CSC-like cells have been identified and characterized. Compelling evidence has revealed that CD44 is involved in the occurrence and development of cancers. Our previous study showed that sphere-forming cells (SFCs) from the human ovarian cancer cell line SKOV-3 had CSC capacity. Therefore, in the present study, we aimed to investigate the effects and mechanisms of the anti-CD44 monoclonal antibody A3D8 on the proliferation and apoptosis of SFCs to explore novel strategies for the treatment of ovarian cancer. Methods: We investigated the effects and mechanisms of A3D8 on the proliferation and apoptosis of SFCs using the MTS assay, cell cycle analysis, an annexin V-fluorescein isothiocyanate/propidium iodide kit, Rh123 apoptosis detection kit, real-time reverse transcription polymerase chain reaction and Western blotting. Results: After CD44 ligation by A3D8, SFC cell proliferation was notably attenuated, cell cycle progression was arrested in the S phase, and apoptosis was significantly increased. The effect of A3D8 was enhanced in a dose- and time-dependent manner, and the effect of apoptosis induction by DDP was enhanced by combination treatment with A3D8. Furthermore, the messenger RNA expression levels of p21 and caspase-3 were up-regulated, whereas those of CDK2, cyclinA, and Bcl-2 were down-regulated. The protein expression levels of caspase-3 were up-regulated, whereas those of CDK2, cyclinA, and Bcl-2 were down-regulated. Conclusions: Our findings indicate that anti-CD44 monoclonal antibodies may be a potential strategy for the treatment of human ovarian cancer after conventional therapy via inhibition of growth and the promotion of apoptosis in SFCs with stemness.
机译:目的:已鉴定并鉴定了CD44 +人卵巢癌干细胞(CSC)和CSC样细胞。有力的证据表明,CD44参与了癌症的发生和发展。我们先前的研究表明,来自人类卵巢癌细胞系SKOV-3的球形细胞(SFC)具有CSC能力。因此,在本研究中,我们旨在研究抗CD44单克隆抗体A3D8对SFC增殖和凋亡的作用和机制,以探索治疗卵巢癌的新策略。方法:我们使用MTS分析,细胞周期分析,膜联蛋白V-异硫氰酸荧光素/碘化丙啶试剂盒,Rh123细胞凋亡检测试剂盒,实时逆转录聚合酶链反应,研究了A3D8对SFC增殖和凋亡的作用和机制。和蛋白质印迹。结果:A3D8连接CD44后,SFC细胞增殖明显减弱,细胞周期进程被阻止在S期,凋亡明显增加。通过与A3D8的联合处理,A3D8的作用以剂量和时间依赖性的方式增强,并且通过DDP诱导的细胞凋亡的作用得到增强。此外,p21和caspase-3的信使RNA表达水平上调,而CDK2,cyclinA和Bcl-2的信使RNA表达下调。 caspase-3的蛋白表达水平上调,而CDK2,cyclinA和Bcl-2的蛋白表达水平下调。结论:我们的发现表明,抗CD44单克隆抗体可能是通过抑制生长和促进具有干性的SFC的凋亡而在常规治疗后治疗人类卵巢癌的潜在策略。

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