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Berberine attenuates XRCC1‐mediated base excision repair and sensitizes breast cancer cells to the chemotherapeutic drugs

机译:小ber碱减弱XRCC1介导的碱基切除修复并使乳腺癌细胞对化疗药物敏感

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摘要

Berberine (BBR) is a natural isoquinoline alkaloid, which is used in traditional medicine for its anti‐microbial, anti‐protozoal, anti‐diarrhoeal activities. Berberine interacts with DNA and displays anti‐cancer activities, yet its effects on cellular DNA repair and on synthetic treatments with chemotherapeutic drugs remain unclear. In this study, we investigated the effects of BBR on DNA repair and on sensitization of breast cancer cells to different types of DNA damage anti‐tumoural drugs. We found BBR arrested cells in the cell cycle S phase and induced DNA breaks. Cell growth analysis showed BBR sensitized MDA‐MB‐231 cells to cisplatin, camptothecin and methyl methanesulfonate; however, BBR had no synergistic effects with hydroxurea and olaparib. These results suggest BBR only affects specific DNA repair pathways. Western blot showed BBR down‐regulated XRCC1 expressions, and the rescued XRCC1 recovered the resistance of cancer cells to BBR. Therefore, we conclude that BBR interferes with XRCC1‐mediated base excision repair to sensitize cancer cells to chemotherapeutic drugs. These finding can contribute to understanding the effects of BBR on cellular DNA repair and the clinical employment of BBR in treatment of breast cancer.
机译:小ber碱(BBR)是一种天然的异喹啉生物碱,由于其抗微生物,抗原生动物,腹泻的活性而被用于传统医学。小ber碱与DNA相互作用并表现出抗癌活性,但其对细胞DNA修复和化学治疗药物综合治疗的作用尚不清楚。在这项研究中,我们研究了BBR对DNA修复以及乳腺癌细胞对不同类型的DNA损伤抗肿瘤药物的敏感性的影响。我们发现BBR阻滞细胞处于细胞周期S期并诱导DNA断裂。细胞生长分析表明,BBR使MDA-MB-231细胞对顺铂,喜树碱和甲磺酸甲酯敏感。但是,BBR与羟脲和奥拉帕尼没有协同作用。这些结果表明,BBR仅影响特定的DNA修复途径。蛋白质印迹显示BBR下调了XRCC1表达,而获救的XRCC1恢复了癌细胞对BBR的抗性。因此,我们得出的结论是,BBR会干扰XRCC1介导的碱基切除修复,从而使癌细胞对化疗药物敏感。这些发现可有助于理解BBR对细胞DNA修复的作用以及BBR在乳腺癌治疗中的临床应用。

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