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Ethacrynic acid improves the antitumor effects of irreversible epidermal growth factor receptor tyrosine kinase inhibitors in breast cancer

机译:乙酸改善不可逆表皮生长因子受体酪氨酸激酶抑制剂在乳腺癌中的抗肿瘤作用

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摘要

Prolonged treatment of breast cancer with epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) often results in acquired resistance and a narrow therapeutic index. One strategy to improve the therapeutic effects of EGFR TKIs is to combine them with drugs used for other clinical indications. Ethacrynic acid (EA) is an FDA approved drug that may have antitumor effects and may enhance the cytotoxicity of chemotherapeutic agents by binding to glutathione and inhibiting WNT signaling. While the α,β-unsaturated-keto structure of EA is similar to that of irreversible TKIs, the mechanism of action of EA when combined with irreversible EGFR TKIs in breast cancer remains unknown. We therefore investigated the combination of irreversible EGFR TKIs and EA. We found that irreversible EGFR TKIs and EA synergistically inhibit breast cancer both in vitro and in vivo. The combination of EGFR TKIs and EA induces necrosis and cell cycle arrest and represses WNT/β-catenin signaling as well as MAPK-ERK1/2 signaling. We conclude that EA synergistically enhances the antitumor effects of irreversible EGFR TKIs in breast cancer.
机译:用表皮生长因子受体(EGFR)酪氨酸激酶抑制剂(TKI)长期治疗乳腺癌通常会导致获得性耐药和狭窄的治疗指数。改善EGFR TKIs治疗效果的一种策略是将它们与用于其他临床适应症的药物联合使用。乙二酸(EA)是FDA批准的药物,可能具有抗肿瘤作用,并且可以通过与谷胱甘肽结合并抑制WNT信号传导来增强化学治疗剂的细胞毒性。虽然EA的α,β-不饱和酮结构与不可逆TKI相似,但与乳腺癌中不可逆EGFR TKI结合使用时EA的作用机理仍然未知。因此,我们研究了不可逆的EGFR TKI和EA的组合。我们发现不可逆的EGFR TKI和EA在体外和体内均协同抑制乳腺癌。 EGFR TKI和EA的组合可诱导坏死和细胞周期停滞,并抑制WNT /β-catenin信号以及MAPK-ERK1 / 2信号。我们得出结论,EA协同增强了不可逆的EGFR TKI在乳腺癌中的抗肿瘤作用。

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