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抗 CD44 单克隆抗体 A3D8 对人卵巢癌细胞球体形成干细胞增殖和凋亡的影响及机制。

Effects and mechanisms of anti-CD44 monoclonal antibody A3D8 on proliferation and apoptosis of sphere-forming cells with stemness from human ovarian cancer.

机构信息

*Department of Immunology of Tianjin Medical University and Tianjin Key Laboratory of Cellular and Molecular Immunology and Key Laboratory of Immune Microenvironment and Disease of Ministry of Education; †Reproductive Medicine Centre, Tianjin Central Hospital for Obstetrics & Gynecology; and ‡Key laboratory of Hormone and Development, Ministry of Health of China and Metabolic Disease Hospital/Institute of Endocrinology, Tianjin Medical University, Tianjin, China.

出版信息

Int J Gynecol Cancer. 2013 Oct;23(8):1367-75. doi: 10.1097/IGC.0b013e3182a1d023.

Abstract

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.

摘要

目的

已鉴定和表征了 CD44(+)人卵巢癌细胞(CSC)和类 CSC 细胞。有强有力的证据表明,CD44 参与了癌症的发生和发展。我们之前的研究表明,人卵巢癌细胞系 SKOV-3 的球体形成细胞(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 增殖和凋亡的影响及其机制,以探索治疗卵巢癌的新策略。

方法

我们使用 MTS 测定法、细胞周期分析、 Annexin V-荧光素异硫氰酸酯/碘化丙啶试剂盒、Rh123 凋亡检测试剂盒、实时逆转录聚合酶链反应和 Western blot 研究了 A3D8 对 SFC 增殖和凋亡的影响及其机制。

结果

A3D8 与 CD44 结合后,SFC 细胞增殖明显减弱,细胞周期停滞在 S 期,凋亡明显增加。A3D8 的作用呈剂量和时间依赖性增强,与 A3D8 联合治疗可增强 DDP 诱导的凋亡作用。此外,p21 和 caspase-3 的信使 RNA 表达水平上调,而 CDK2、cyclinA 和 Bcl-2 的表达水平下调。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

我们的研究结果表明,抗 CD44 单克隆抗体可能是一种通过抑制生长和促进具有干性的 SFC 凋亡来治疗常规治疗后人类卵巢癌的潜在策略。

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