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纸质出版:2012
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蒋心惠,黄开顺,滕永真,何百成,周岐新.汉防己碱对肝癌Hep3b细胞生长的双向作用[J].陆军军医大学学报(原第三军医大学学报),2012,34(13):1281-1284.
Jiang Xinhui,Huang Kaishun,Teng Yongzhen,He Baicheng,Zhou Qixin.Dualistic effects of tetrandrine on growth in human hepatoma 3b cells[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(13):1281-1284.
目的 考察汉防己碱(tetrandrine,Tet)对肝癌Hep3b和Hep3b/5-Fu细胞生长的影响。 方法 采用体外细胞培养,结合流式细胞术、MTT和Western blot方法研究Tet(0.33~1.0 μg/ml)对肝癌Hep3b及Hep3b/5-Fu细胞生长的作用特点。 结果 Tet在0.33~1.0 μg/ml时呈浓度依赖性降低Hep3b细胞存活率;0.5和1.0 μg/ml显著提高5-Fu对Hep3b细胞的IC
50
,但降低5-Fu对Hep3b/5-Fu细胞的IC
50
;0.33 μg/ml的Tet明显增加cDDP对Hep3b/5-Fu细胞的IC
50
,而0.5和1.0 μg/ml显著降低cDDP对Hep3b/5-Fu细胞的IC
50
(P0.01)。1.0 μg/ml的Tet作用48 h后使Hep3b细胞中的P-gp和MRP1表达明显上调(P0.05)。Tet单用对Hep3b细胞生长有一定抑制作用,高浓度Tet逆转Hep3b/5-Fu细胞对5-Fu耐药和增强cDDP对Hep3b/5-Fu细胞生长的抑制作用,但低浓度分别促进Hep3b细胞和Hep3b/5-FU细胞对5-Fu和cDDP耐药。 结论 Tet对Hep3b和Hep3b/5-Fu细胞生长呈浓度相关的双向作用,其促进耐药细胞发展的机制至少与提升P-gp和MRP1表达有关。
Objective To determine the effects of tetrandrine (Tet) on the growth in human hepatoma 3b (Hep3b) cells. Methods Flow cytometry
MTT assay
and Western blotting were used to investigate the effects of Tet (0.33 to 1.0 μg/ml) on the growth of Hep3b and Hep3b/5-Fu cells. Results Tet resulted in a decreased survival rate of Hep3b cells in a dose-dependent manner. Tet of 0.5 and 1.0 μg/ml significantly increased the IC
50
of 5-fluo
rouracil (5-Fu) to Hep3b cells
whereas reduced the IC
50
of 5-FU to Hep3b/5-Fu cells. Tet of 0.33μg/ml significantly increased the IC
50
of Cisplatin (cDDP) to Hep3b/5-Fu cells
but that of 0.5 and 1.0 μg/ml significantly reduced its IC
50
to Hep3b/5-Fu cells. Treatment of 1.0 μg/ml Tet for 48 h obviously resulted in an up-regulation of P-gp and MRP1 in the Hep3b cells (P0.05). Our results indicated that Tet exerted inhibitory effect on Hep3b growth
and it at high concentration reversed the resistance of Hep3b/5-Fu cells to 5-Fu and enhanced the cytotoxic effect of cDDP on these Hep3b/5-Fu cells. Conclusion Tet shows a dose-related dualistic effects on the growth of Hep3b and Hep3b/5-Fu cells
which might be related with the up-regulating of P-gp and MRP1.
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