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细胞毒素-1对人卵巢癌细胞体外增殖、凋亡的影响

Effect of cytotoxin-1 on human ovarian cancer cell proliferation and apoptosis in vitro
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摘要 目的探讨细胞毒素-1(Cytotoxin-1,CTX-1)对人卵巢癌SKOV-3细胞增殖凋亡的影响。方法利用0、4、8、12μg/mL浓度CTX-1处理SKOV-3细胞6、12、24 h,MTS法检测细胞活性,8μg/mL CTX-1处理SKOV-3细胞24、48 h,Hoechst-33258荧光染色观察细胞核染色质形态。取处理6、12 h后细胞,利用流式细胞仪检测SKOV-3细胞的凋亡率。结果4、8、12μg/mL的CTX-1可抑制SKOV-3细胞活性及增殖,呈时间-剂量依赖。Hoechst-33258染色观察可见细胞染色质呈固缩或碎裂状、染色质着色不均、核形态各异,随时间增加而更趋明显。8μg/mL CTX-1处理细胞,6 h细胞坏死率为(1.90±0.27)%,晚期凋亡率为(10.96±1.56)%,而早期凋亡率为(1.52±0.39)%;12 h细胞坏死率为(10.62±0.96)%,晚期凋亡率(15.07±1.23)%,而早期凋亡率为(1.88±0.17)%,与对照组比较,差异有统计学意义(P<0.01)。结论CTX-1可以抑制人卵巢癌细胞活性、抑制其体外增殖、诱导其发生凋亡,该作用呈剂量依赖和时间依赖,主要引起细胞晚期凋亡和坏死。 Objective To investigate the effect of cytotoxin-1(CTX-1)on the proliferation and apoptosis of ovarian cancer SKOV-3 cells.Methods SKOV-3 cells were treated with CTX-1 at concentrations of 0,4,8,12μg/mL for 6,12,and 24 hours respectively.Cell viability was measured by MTS method.SKOV-3 cells were treated with 8μg/mL CTX-1 for 24 and 48 hours,by Hoechst-33258 fluorescence staining to observe the morphology of nuclear chromatin.The apoptotic rate of SKOV-3 cells was detected by flow cytometry after 6 and 12 hours of treatment.Results CTX-1 at 4,8,and 12μg/mL inhibited the activity and proliferation of SKOV-3 cells in a time-dose-dependent manner.Hoechst-33258 staining observation showed that the apoptotic cell chromatin was condensed or fragmented chromatin,the chromatin was unevenly colored,and the nuclear morphology was different.It became more obvious with time.8μg/mL CTX-1 treated cells,the 6 h cell necrosis rate was(1.90±0.27)%,the late apoptosis rate was(10.96±1.56)%,and the early apoptosis rate was(1.52±0.39)%;12 hours cell necrosis rate was(10.62±0.96)%,late apoptosis rate was(15.07±1.23)%,and early apoptosis rate was(1.88±0.17)%,compared with the control group,the difference was statistically significant(P<0.01).Conclusion CTX-1 may inhibit the activity of human ovarian cancer cells,inhibit its proliferation in vitro,and induce its apoptosis.The effect is dose-dependent and time-dependent.Mainly it causes late apoptosis and necrosis of cells.
作者 黄千峰 武丽 欧燕兰 艾君 张秀 HUANG Qianfeng;WU Li;OU Yanlan;AI Jun;ZHANG Xiu(Guangdong Women and Children Hospital,Guangzhou 511400,China)
出处 《广州医药》 2020年第6期24-27,32,共5页 Guangzhou Medical Journal
基金 中国疾病预防控制中心妇幼保健中心科研项目(2019FYH003)。
关键词 细胞毒素-1 人卵巢癌SKOV-3细胞 增殖 凋亡 Cytotoxin-1 Human ovarian cancer SKOV-3 cells Proliferation Apoptosis
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  • 1李晓红,蔡绍晖,任先达.蛇毒的抗肿瘤活性成分研究进展[J].中国病理生理杂志,2004,20(10):1938-1941. 被引量:17
  • 2朱坤祥.眼镜蛇毒抗肝癌作用研究[J].新消化病学杂志,1996,4(8):436-437. 被引量:9
  • 3杜雨苍 吴文玉 等.一个新的蛇毒细胞膜毒素D1的分离及鉴定[J].生理化学与生物物理学报,1985,17(2):199-206. 被引量:3
  • 4Debnath A,Saha A,Gomes A,et al.A lethal cardiotoxic-cytotoxic protein from the Indian monocellate cobra (Naja kaouthia)venom. Toxicon . 2010 被引量:1
  • 5Chen XY,,Yang HX,Qu SF,et al.Involvement of p38and c-Jun N-terminal protein kinase in cardiotoxin III-induced apoptosis of K562 cells. Biological and Pharmaceutical Bulletin . 2009 被引量:1
  • 6Yang SH,Chien CM,Lu MC,et al.Up-regulation ofBax and endonuclease G,and down-modulation of Bcl-XL involved in cardiotoxin III-induced apoptosis in K562cells. Experimental and Molecular Medicine . 2006 被引量:1
  • 7Feofanov AV,Sharonov GV,Arseniev AS, et al.Cancer cell injury by cytotoxins from cobra venom is mediated through lysosomal damage. Biochemical Journal . 2005 被引量:1
  • 8Yang S H,Chien C M,Chang L Set al.Involvementof c-junN-terminal kinasein G2/Marrest and caspase-mediated apoptosis induced by cardiotoxin III (Najanaja atra)in K562 leukemia cells. Toxicon . 2007 被引量:1
  • 9Tjong SC,Wu PL,Wang CM,et al.Role of glycosphingolipid conformational change in membrane pore forming activity of cobra cardiotoxin. Biochemistry . 2007 被引量:1
  • 10Chen KC,Lin SR,ChangLS.Involvementofmitochondrial altera-tion and reactive oxygen species generation in Taiwan cobra cardio-toxin-induced apoptotic death of human neuroblastoma SK-N-SH cells. Toxicon . 2008 被引量:1

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