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金属硫蛋白对人宫颈癌细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2007, 34(12): 924-926. DOI: 10.3971/j.issn.1000-8578.62
引用本文: 金属硫蛋白对人宫颈癌细胞增殖和凋亡的影响[J]. 肿瘤防治研究, 2007, 34(12): 924-926. DOI: 10.3971/j.issn.1000-8578.62
Effects on Proliferation and Apoptosis in Human Cervical Cancer Cells Treated with Metallothionein[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 924-926. DOI: 10.3971/j.issn.1000-8578.62
Citation: Effects on Proliferation and Apoptosis in Human Cervical Cancer Cells Treated with Metallothionein[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 924-926. DOI: 10.3971/j.issn.1000-8578.62

金属硫蛋白对人宫颈癌细胞增殖和凋亡的影响

Effects on Proliferation and Apoptosis in Human Cervical Cancer Cells Treated with Metallothionein

  • 摘要: 目的 探讨金属硫蛋白(metallothionein,MT)对人宫颈癌细胞HeLa增殖和凋亡的影响并初步分析其机制。方法 以不同浓度的MT(0.001、0.01、0.1和1ng/m1)干预HeLa细胞,MTT法测定其对细胞 增殖的促进作用,流式细胞仪分析凋亡率,免疫细胞化学法和RT-PIER法测定p53和PCNA的表达。结果 (1)MT对HeLa细胞增殖表现出浓度依赖性的促进作用,以1ng/ml时作用最明显(P〈0.05)。(2)MT可抑制细胞凋亡,其浓度为0、0.01和1ng/ml时,凋亡指数(AJ)分别为(6.35±1.08)%、(4.45±0.95)%和(2.15±0.77)%。(3)MT作用后细胞p53表达显著减弱,PCNA表达显著增强,两者均呈浓度依赖性。结论 MT对人宫颈癌HeLa细胞具有显著地促进增殖和抑制凋亡作用,其机制可能与抑制p53基因表达有关。

     

    Abstract: Objective  To study the effects of metallothionein on the proliferation and apoptosis of human cervical cell HeLa and their initiatory mechanism. Methods  Add MT of different concent ration to HeLa cell, MTT assay was used to analyze proliferative rate and apoptosis was measured by flow cytometry, immunocytochemistry and RT-PCR were used to detect expression of p53 and PCNA. Results  (1) Metallothionein exerted proliferation effect on HeLa cell in a concent ration-dependent way and the effect was most obviously in 1ng/ ml ( P < 0. 05) . (2) Apoptosis was inhibited by MT, and AI was 6. 35 ±1. 08 、4. 45 ±0. 95 and 2. 15 ±0. 77 when MT was on 0 、0. 01 and 1 ng/ ml. (3) The expression of p53 was significantly decreased and PCNA was significantly increased af ter MT treatment, and the effects were concent ration-dependent . Conclusion  Metallothionein can enhance proliferation and inhibit apoptosis of human cervical cell HeLa, maybe through inhibiting the expression of p53 gene.

     

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