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The Sequence-Dependent Cytotoxic Effect of Trastuzumab in Combination With 5-Fluorouracil or Cisplatin on Gastric Cancer Cell Lines

机译:曲妥珠单抗联合5-氟尿嘧啶或顺铂对胃癌细胞株的序列依赖性细胞毒作用

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The effect of trastuzumab on patients with HER-2eu (HER2)-positive gastric cancer has been confirmed in a phase III clinical trial (ToGA study). However, the optimized sequence and synergic mechanism of trastuzumab and chemotherapy are not clear. Our study investigated the effects and mechanisms of trastuzumab in combination with 5-Fluorouracil (5-Fu) or cisplatin (DDP) on gastric cancer cell lines. Flow cytometry was used to determine HER2 expression and cell cycle. MTT assay was performed to evaluate cytotoxicity. Western blotting and RT-PCR were used to analyze signaling transduction and mRNA expression. Sequential 5-Fu followed by trastuzumab and trastuzumab plus DDP followed by trastuzumab produced the best inhibitory effects. Inhibition of HER2-PI3K-AKT signal transduction, downregulation of nucleotide excision repair cross-complementation 1 (ERCC1), and interference with cell cycle distribution may elucidate the synergism between trastuzumab and chemotherapy. These results provide some evidence for designing a rational regime when trastuzumab is being considered to be used in patients with gastric cancer.
机译:一项III期临床试验(ToGA研究)已证实曲妥珠单抗对HER-2 / neu(HER2)阳性胃癌患者的影响。然而,曲妥珠单抗与化学疗法的优化序列和协同机制尚不清楚。我们的研究调查了曲妥珠单抗联合5-氟尿嘧啶(5-Fu)或顺铂(DDP)对胃癌细胞系的作用及其机制。流式细胞仪用于确定HER2表达和细胞周期。进行MTT测定以评价细胞毒性。 Western blotting和RT-PCR用于分析信号转导和mRNA表达。依次5-Fu,曲妥珠单抗,曲妥珠单抗加DDP,曲妥珠单抗的抑菌效果最佳。 HER2-PI3K-AKT信号转导的抑制,核苷酸切除修复交叉互补1(ERCC1)的下调以及对细胞周期分布的干扰可能阐明了曲妥珠单抗与化学疗法之间的协同作用。这些结果为当曲妥珠单抗被认为用于胃癌患者时设计合理方案提供了一些证据。

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