首页> 美国卫生研究院文献>Cancer Science >An Anti‐GD2 Monoclonal Antibody Enhances Apoptotic Effects of Anti‐cancer Drugs against Small Cell Lung Cancer Cells via JNK (c‐Jun Terminal Kinase) Activation
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An Anti‐GD2 Monoclonal Antibody Enhances Apoptotic Effects of Anti‐cancer Drugs against Small Cell Lung Cancer Cells via JNK (c‐Jun Terminal Kinase) Activation

机译:抗GD2单克隆抗体通过JNK(c-Jun终端激酶)激活增强抗癌药对小细胞肺癌细胞的凋亡作用。

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摘要

Small cell lung cancer (SCLC) cell lines specifically express ganglioside GD2, and anti‐GD2 monoclonal antibodies (mAbs) caused suppression of cell growth and induced apoptosis of SCLC cells with single use. Here, enhancement of the cytotoxic effects of various anti‐cancer drugs with an anti‐GD2 mAb was demonstrated. The cytotoxicity of all six drugs examined was markedly enhanced, i.e. 2.4–7.8–fold increase of cell sensitivity in terms of IC50. In particular, the combination of cisplatin (CDDP) with an anti‐GD2 mAb resulted in prominent enhancement of cytotoxicity even in low‐moderate GD2–expressing lines. The anti‐GD2 mAb induced weak activation of c‐Jun terminal kinase (JNK) in SCLC cells, and all anti‐cancer drugs also induced its activation to various degrees. When CDDP and an anti‐GD2 mAb were used together, significantly stronger JNK activation was observed corresponding to the cytotoxic effects, suggesting that synergistic phosphorylation of JNK with two reagents induced prominent apoptosis. The essential role of JNK in the induction of SCLC apoptosis with CDDP and anti‐GD2 mAb was confirmed by experiments with a JNK inhibitor, curcumin. These results suggest that anti‐GD2 mAbs would be very efficient in combination with anti‐cancer drugs, both to achieve SCLC‐specific cytotoxicity and to enhance its magnitude.
机译:小细胞肺癌(SCLC)细胞系特异性表达神经节苷脂GD2,而抗GD2单克隆抗体(mAbs)一次使用可抑制细胞生长并诱导SCLC细胞凋亡。在此证明了使用抗GD2 mAb增强了各种抗癌药物的细胞毒性作用。检测的所有六种药物的细胞毒性均显着增强,即以IC50计,细胞敏感性提高了2.4–7.8倍。尤其是,顺铂(CDDP)与抗GD2 mAb的组合即使在中度表达GD2的低表达细胞系中也能显着增强细胞毒性。抗GD2 mAb诱导了SCLC细胞中c-Jun末端激酶(JNK)的弱激活,所有抗癌药物也都不同程度地诱导了其激活。当CDDP和抗GD2 mAb一起使用时,观察到明显更强的JNK激活,这与细胞毒性作用相对应,表明JNK与两种试剂的协同磷酸化可诱导显着的细胞凋亡。 JNK抑制剂姜黄素的实验证实了JNK在CDDP和抗GD2 mAb诱导SCLC凋亡中的重要作用。这些结果表明,抗GD2单克隆抗体与抗癌药物联合使用将非常有效,既可实现SCLC特异性细胞毒性,又可提高其强度。

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