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Combination of lapatinib with isothiocyanates overcomes drug resistance and inhibits migration of HER2 positive breast cancer cells

机译:拉帕替尼与异硫氰酸盐的组合可克服耐药性并抑制HER2阳性乳腺癌细胞的迁移

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摘要

BackgroundLapatinib is a commonly used drug that interrupts signaling from the epidermal growth factor receptors, EGFR and HER2eu. Long-term exposure to lapatinib during therapy eliminates cells that are sensitive to the drug; however, at the same time it increases probability of lapatinib-resistant cell selection. The aim of this study was to verify whether combinations of lapatinib with one of isothiocyanates (sulforaphane, erucin or sulforaphene), targeting different levels of HER2 signaling pathway, exert stronger cytotoxic effect than therapy targeting the receptor only, using heterogeneous populations consisting of lapatinib-sensitive and lapatinib-resistant breast cancer cells.
机译:背景拉帕替尼是一种常用的药物,可中断表皮生长因子受体EGFR和HER2 / neu的信号传导。治疗期间长期接触拉帕替尼会消除对药物敏感的细胞;然而,与此同时,它增加了对拉帕替尼耐药的细胞选择的可能性。这项研究的目的是通过使用由lapatinib-组成的异质性群体,验证lapatinib与异硫氰酸酯之一(萝卜硫烷,芥酸或磺草芬)的组合是否靶向HER2信号通路的不同水平,比仅靶向受体的治疗具有更强的细胞毒性作用。敏感且抗拉帕替尼的乳腺癌细胞。

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