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survivin 及bcl-2 基因表达在胃癌细胞株MGC803 顺铂耐药中的作用[J]. 肿瘤防治研究, 2007, 34(01): 24-27. DOI: 10.3971/j.issn.1000-8578.2448
引用本文: survivin 及bcl-2 基因表达在胃癌细胞株MGC803 顺铂耐药中的作用[J]. 肿瘤防治研究, 2007, 34(01): 24-27. DOI: 10.3971/j.issn.1000-8578.2448
The Affection of survivin and bcl-2 mRNA Expression on Drug- resistance of Gastric Cancer Cell Line MGC803 to Cisplatin[J]. Cancer Research on Prevention and Treatment, 2007, 34(01): 24-27. DOI: 10.3971/j.issn.1000-8578.2448
Citation: The Affection of survivin and bcl-2 mRNA Expression on Drug- resistance of Gastric Cancer Cell Line MGC803 to Cisplatin[J]. Cancer Research on Prevention and Treatment, 2007, 34(01): 24-27. DOI: 10.3971/j.issn.1000-8578.2448

survivin 及bcl-2 基因表达在胃癌细胞株MGC803 顺铂耐药中的作用

The Affection of survivin and bcl-2 mRNA Expression on Drug- resistance of Gastric Cancer Cell Line MGC803 to Cisplatin

  • 摘要: 目的 探讨胃癌细胞株MGC803对顺铂(CDDP)耐药产生的有关机制。方法 观察不同浓度CDDP(0.1、1.0、10.0mg/L)对MGC803细胞增殖、凋亡及抗凋亡基因survivin,bcl-2 mRNA表达的影响,用MTT法检测细胞生长抑制率;荧光染色检测细胞凋亡率;流式细胞仪测定细胞周期的变化;RT-PCR检测survivin、bcl-2 mRNA的表达。结果 10mg/L的CDDP对MGC803细胞有较强的抑制增殖、促进凋亡作用,而0.1、1.0mg/L的CDDP干预24h后,其抑制细胞增殖,促进细胞凋亡的作用逐渐消失;CDDP作用于细胞48h后,细胞S期增加,G2/M期下降;MGC803细胞在1.0mg/L的CDDP作用下,survivin mRNA表达自24h后逐渐增高,bcl-2 mRNA表达逐渐下降(P〈0.05)。结论 CDDP可干扰MGC803细胞周期,但该细胞对低浓度CDDP易于产生耐药,survivin mRNA表达增高可能是MGC803细胞对CDDP产生耐药原因之一。

     

    Abstract: Objective  To investigate the drug-resistance mechanisms of gastric cancer cell to cisplatin (CDDP) . Methods  Gast ric cancer cell line MGC803 were t reated by CDDP (0. 1, 1. 0, 10. 0mg/ L) for 12, 24, 48 and 72hours. Proliferation was detected by MTT assay and apoptosis was measured by fluorescence staining. Cell cycle was detected by flow cytomet ry. survivin and bcl-2 mRNA expression were detected by RT-PCR. Results  High concent ration of CDDP (10. 0mg/ L) could inhibit proliferation and induce apoptosis, but low concent ration of CDDP(0. 1, 1. 0mg/ L) did not . the effect s of inhibiting proliferation and inducing apoptosis did not increase significantly af ter 24 hours, The cell cycle was altered af ter the cells were t reated by CDDP. S phase of cells were increased and G2 / M phase of cells were decreased. survivin mRNA expression increased and bcl22 mRNA expression decreased gradually af ter t reated by CDDP(1. 0mg/ L) for 24h ( P < 0. 05) . Conclusion  CDDP could arrest the cell cycle on MGC803 cell. But the cells were easily developing drug-resistance to low concent ration of CDDP. Over expression of survivin mRNA may be one of the mechanisms of drug resistance in MGC803 cells.

     

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