Gong Soo Jung, Jin Choon Jo, Rha Sun Young, Chung Hyun Cheol
Department of Internal Medicine, Eulji University School of Medicine, Seoul, South Korea.
Cancer Lett. 2004 Oct 28;214(2):215-24. doi: 10.1016/j.canlet.2004.04.029.
The various treatments for advanced gastric cancer have limitations and induce only marginal survival benefit. HER-2/neu protein is overexpressed in several types of human cancers and its amplification is associated with poor prognosis. Recombinant humanized anti-HER-2/neu antibody (trastuzumab) not only inhibits the proliferation of HER-2/neu overexpressing tumor cells but also augments the cytotoxicity of concomitant chemotherapeutic agents in metastatic breast cancer. In this study, we evaluated the growth inhibitory effects of trastuzumab in gastric cancer cells. HER-2/neu protein was evaluated by immunohistochemical analysis in seven gastric cancer cell lines. MTT assay was performed to evaluate the growth inhibitory effects of trastuzumab and three chemotherapeutic agents, doxorubicin, cisplatin and paclitaxel, both alone and in combinations. The changes of cell cycle after trastuzumab treatment were analyzed by flow cytometry. Four of the cell lines, YCC-2 with strong positivity of HER-2/neu expression, NCI-N87 with moderate positivity, YCC-3 with weak positivity, and SK-BR-3 as a positive control, were selected. After in vitro MTT assay for 1-day and 5 consecutive days' treatment of trastuzumab at various concentrations, growth inhibition was not observed in any cancer cell lines. However, there was variable dose-dependent sensitivity to doxorubicin, cisplatin and paclitaxel. YCC-2 and SK-BR-3 cancer cells were more sensitive to three chemotherapeutic drugs, constantly (P<0.05). The combination of 5 consecutive days' treatment of trastuzumab with 1-day doxorubicin treatment showed significant growth inhibition only in YCC-2 and NCI-N87 gastric cancer cells. After 1-day trastuzumab treatment, the S-phase fraction was decreased by 52 and 70% in YCC-2 and SK-BR-3, respectively. In conclusion, the expressions of HER-2/neu protein in gastric cancer cells are variable, and concomitant treatments of trastuzumab with doxorubicin increase cytotoxicity. This suggests that trastuzumab-based biologic therapy with chemotherapeutic agents can be applied in gastric cancer treatment.
晚期胃癌的各种治疗方法都存在局限性,仅能带来有限的生存获益。HER-2/neu蛋白在多种人类癌症中过度表达,其扩增与预后不良相关。重组人源化抗HER-2/neu抗体(曲妥珠单抗)不仅能抑制HER-2/neu过表达肿瘤细胞的增殖,还能增强转移性乳腺癌中联合化疗药物的细胞毒性。在本研究中,我们评估了曲妥珠单抗对胃癌细胞的生长抑制作用。通过免疫组化分析评估了7种胃癌细胞系中HER-2/neu蛋白的表达情况。进行MTT试验以评估曲妥珠单抗及三种化疗药物(阿霉素、顺铂和紫杉醇)单独及联合使用时的生长抑制作用。通过流式细胞术分析曲妥珠单抗处理后细胞周期的变化。选择了4种细胞系,HER-2/neu表达强阳性的YCC-2、中度阳性的NCI-N87、弱阳性的YCC-3以及作为阳性对照的SK-BR-3。在体外进行MTT试验,用不同浓度的曲妥珠单抗处理1天和连续处理5天,未在任何癌细胞系中观察到生长抑制。然而,对阿霉素、顺铂和紫杉醇存在不同程度的剂量依赖性敏感性。YCC-2和SK-BR-3癌细胞对三种化疗药物更敏感,差异具有统计学意义(P<0.05)。曲妥珠单抗连续处理5天与阿霉素处理1天联合使用仅在YCC-2和NCI-N87胃癌细胞中显示出显著的生长抑制。曲妥珠单抗处理1天后,YCC-2和SK-BR-3的S期比例分别下降了52%和70%。总之,胃癌细胞中HER-2/neu蛋白的表达存在差异,曲妥珠单抗与阿霉素联合治疗可增加细胞毒性。这表明基于曲妥珠单抗的生物治疗联合化疗药物可应用于胃癌治疗。