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DcR3对乳腺癌细胞凋亡的影响及其在乳腺癌血清中的表达[J]. 肿瘤防治研究, 2011, 38(07): 784-787. DOI: 10.3971/j.issn.1000-8578.2011.07.015
引用本文: DcR3对乳腺癌细胞凋亡的影响及其在乳腺癌血清中的表达[J]. 肿瘤防治研究, 2011, 38(07): 784-787. DOI: 10.3971/j.issn.1000-8578.2011.07.015
Effect of DcR3 on Apoptosis of Breast Carcinoma Cells and Expression in Sera of Breast Carcinoma Patients[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 784-787. DOI: 10.3971/j.issn.1000-8578.2011.07.015
Citation: Effect of DcR3 on Apoptosis of Breast Carcinoma Cells and Expression in Sera of Breast Carcinoma Patients[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 784-787. DOI: 10.3971/j.issn.1000-8578.2011.07.015

DcR3对乳腺癌细胞凋亡的影响及其在乳腺癌血清中的表达

Effect of DcR3 on Apoptosis of Breast Carcinoma Cells and Expression in Sera of Breast Carcinoma Patients

  • 摘要: 目的研究诱捕受体3(DcR3)单克隆中和性抗体对乳腺癌细胞生长和凋亡的影响,以及DcR3在乳腺癌患者血清中的表达及临床意义。方法将DcR3单克隆中和性抗体作用于体外培养的人乳腺癌细胞系MCF-7,检测细胞增殖情况及Caspase 3/7活性变化,应用Hoechst 33342及碘化丙啶双重染色荧光显微镜下观察细胞凋亡形态及计算凋亡率。应用ELISA检测乳腺癌患者血清中DcR3的表达。结果DcR3中和性抗体可抑制MCF-7细胞生长并可诱导细胞凋亡(P<0.05)。乳腺癌患者血清DcR3 水平明显高于健康对照组(P<0.01);DcR3表达水平与肿瘤大小及临床TNM分期有关(P<0.05)。结论DcR3对人乳腺癌细胞增殖具有抑制作用,其机制与诱导肿瘤细胞凋亡有关。DcR3与乳腺癌的发生及恶性进展有关,检测DcR3血清表达有助于乳腺癌诊断及预后判断。

     

    Abstract: ObjectiveTo study the effect of anti-human decoy receptor 3(DcR3)neutralization monoclonal antibody on growth and apoptosis of breast carcinoma cell,and to explore the expression and clinical significance of DcR3 in the sera of breast carcinoma patients. MethodsHuman breast carcinoma cell line MCF-7 was treated with anti-DcR3 monoclonal antibody in vitro. Cell viability and Caspase 3/7 activity were evaluated by CellTiter-Blue Cell Viability Assay and Apo-ONE Homogeneous Caspase-3/7 Assay, respectively. Morphology and the apoptotic rate were assessed by Hoechst 33342 and propidium iodide double fluorescent chromatin staining. Expression of DcR3 in the sera of breast carcinoma patients was performed with ELISA. ResultsDcR3 monoclonal antibody inhibited the growth and induced the apoptosis of breast carcinoma MCF-7 cells(P<0.05).The expression of DcR3 in the sera of breast carcinoma patients was significantly higher than that in healthy controls(P<0.01).The expression of sera DcR3 was correlated to tumor size and clinical TNM stages(P<0.05). ConclusionDcR3 has the effect on inhibiting cell viability in breast carcinoma cells,which may be related to the apoptosis. DcR3 is associated with the tumorigenesis and progress of breast carcinoma, and detection of sera DcR3 expression could contribute to the diagnosis and prognosis of breast carcinoma patients.

     

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