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A new mechanism of drug resistance in breast cancer cells: fatty acid synthase overexpression-mediated palmitate overproduction.

机译:乳腺癌细胞耐药性的新机制:脂肪酸合酶过度表达介导的棕榈酸酯过度生产。

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摘要

Multidrug resistance is a major problem in successful cancer chemotherapy. Various mechanisms of resistance, such as ABC transporter-mediated drug efflux, have been discovered using established model cancer cell lines. While characterizing a drug-resistant breast cancer cell line, MCF7/AdVp3000, we found that fatty acid synthase (FASN) is overexpressed. In this study, we showed that ectopic overexpression of FASN indeed causes drug resistance and that reducing the FASN expression increased the drug sensitivity in breast cancer cell lines MCF7 and MDA-MB-468 but not in the normal mammary epithelial cell line MCF10A1. Use of FASN inhibitor, Orlistat, at low concentrations also sensitized cells with FASN overexpression to anticancer drugs. The FASN-mediated drug resistance appears to be due to a decrease in drug-induced apoptosis from an overproduction of palmitic acid by FASN. Together with previous findings of FASN as a poor prognosis marker for breast cancer patients, our results suggest that FASN overexpression is a new mechanism of drug resistance and may be an ideal target for chemosensitization in breast cancer chemotherapy.
机译:多药耐药性是成功进行癌症化疗的主要问题。使用建立的模型癌细胞系已经发现了多种耐药机制,例如ABC转运蛋白介导的药物外流。在表征耐药性乳腺癌细胞系MCF7 / AdVp3000时,我们发现脂肪酸合酶(FASN)过度表达。在这项研究中,我们表明异位表达的FASN确实会引起耐药性,降低FASN的表达会增加乳腺癌细胞MCF7和MDA-MB-468中的药物敏感性,但不会影响正常的乳腺上皮细胞MCF10A1中的药物敏感性。以低浓度使用FASN抑制剂Orlistat也会使FASN过表达的细胞对抗癌药物敏感。 FASN介导的耐药性似乎是由于FASN过量生产棕榈酸导致药物诱导的凋亡减少。结合FASN先前发现的乳腺癌患者不良预后指标,我们的结果表明FASN过表达是一种新的耐药机制,并且可能是乳腺癌化学疗法中化学增敏的理想靶标。

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