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川芎嗪联合氟尿嘧啶对胃癌细胞SGC-7901/ADR的杀伤作用[J]. 肿瘤防治研究, 2008, 35(09): 624-626. DOI: 10.3971/j.issn.1000-8578.1805
引用本文: 川芎嗪联合氟尿嘧啶对胃癌细胞SGC-7901/ADR的杀伤作用[J]. 肿瘤防治研究, 2008, 35(09): 624-626. DOI: 10.3971/j.issn.1000-8578.1805
Lethal Effect of Combination of Tetramethylpyrazine and Fluorouracil in Multidrug Resistance of Gastric Carcinoma Cell Lines SGC-7901/ADR[J]. Cancer Research on Prevention and Treatment, 2008, 35(09): 624-626. DOI: 10.3971/j.issn.1000-8578.1805
Citation: Lethal Effect of Combination of Tetramethylpyrazine and Fluorouracil in Multidrug Resistance of Gastric Carcinoma Cell Lines SGC-7901/ADR[J]. Cancer Research on Prevention and Treatment, 2008, 35(09): 624-626. DOI: 10.3971/j.issn.1000-8578.1805

川芎嗪联合氟尿嘧啶对胃癌细胞SGC-7901/ADR的杀伤作用

Lethal Effect of Combination of Tetramethylpyrazine and Fluorouracil in Multidrug Resistance of Gastric Carcinoma Cell Lines SGC-7901/ADR

  • 摘要: 目的观察川芎嗪(TMP)联合氟尿嘧啶(5-Fu)对胃癌多药耐药细胞SGC7901/ADR细胞的体外杀伤作用。方法采用MTT法观察TMP联合5-Fu对SGC7901/ADR细胞的杀伤作用,光镜下观察并采用流式细胞仪(FCM)测定各药物组细胞周期的分布。结果5-Fu对SGC-7901/ADR细胞的半数抑制率(IC50)为13.001mg/L,与300mg/LTMP联合后,使其的IC50降至1.542mg/L,逆转倍数是8.43倍,与对照组相比差异具有统计学意义(P<0.01)。光镜下可见5-Fu+TMP(终浓度300mg/L)组较5-Fu组癌细胞皱缩变小变圆,出现凋亡改变。FCM分析:TMP联合5-Fu与对照组相比将细胞阻滞在DNA合成前期和静息期-G0/G1期(P<0.05)。结论TMP与5-Fu联合对胃癌多药耐药细胞SGC7901/ADR有较强的杀伤作用,为当前胃癌治疗提供了新思路。

     

    Abstract: Objective To investigate the lethal effect of combination of TMP and 5-Fu in the multidrug resistance of Gastric Carcinoma Cell Lines SGC-7901/ADR. Methods Gastric carcinoma cell lines SGC-7901 and the multidrug resistance cell lines SGC-7901/ADR were considered as target cells, MTT assay was used to investigate the lethal effect of combination of TMP and 5-Fu in vitro,which was observed by Light microscope. Flow cytometer(FCM) was employed to investigate the cell cycles. Results The half inhibition ratio(IC50 ) of 5-Fu against SGC-7901/ ADR was 13. 001 mg/ L, which was reduced to 1. 542mg/ L by 300 mg/ L TMP, The reversal index was 8. 43 ( P < 0. 01) . Malignant cell volume and morphous which exposed to 5-Fu + TMP became smaller and st rinked rounder by Light microscope. FCM revealed that with the effect of 5-Fu + TMP, cell cycle was blocked at presynthetic phase and ambiguous phase-G0 /G1 phase and The cells enter the period of DNA synthesis were reduced, inhibition mitosis of SGC-7901/ADR( P < 0. 05) . Conclusion  Combination of 5-Fu and TMP has st ronger lethal effect against the multidrugs resistance Cell Lines SGC-7901/ ADR in Gast ric Carcinoma, which may provid a new therapeusis against Gast ric Carcinoma.

     

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