ABCC1促进gsh依赖性铁转运和对Fe(II)和Cu(II)螯合剂的抗性。

IF 3.6 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anikó Gaál, Lúcia Torma, Éva Bakos, Katalin Német, Peter Kregsamer, Christina Streli, Miklós Péter Mohai, Elina Üveges, Julia H Bormio Nunes, Petra Heffeter, Gergely Szakács, Norbert Szoboszlai
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引用次数: 0

摘要

治疗耐药是癌症治疗的主要挑战,多药耐药(MDR)是一种很有特征的现象,其中癌细胞不仅对给药药物产生耐药,而且对结构多样的化合物产生耐药。金属螯合剂,包括喹啉类和硫代氨基脲类,已经显示出广泛的抗肿瘤活性和通过调节金属代谢来克服耐多药的潜力。然而,预测螯合剂是否增加或减少耐多药细胞的毒性仍然很复杂,特别是螯合剂-金属复合物可能成为atp结合盒(ABC)转运体的底物,导致耐药性或超敏性。在这项研究中,我们开发了三种主要MDR ABC转运体(ABCB1、ABCC1和ABCG2)表达水平相当的细胞系。我们的研究结果表明,转运蛋白对螯合剂毒性有明显的特异性影响。表达ABCC1的细胞对无金属和金属结合形式的硫代氨基脲(Dp44mT, COTI-2, DpC)均表现出明显的抗性。水泡运输实验进一步证明,ABCC1能主动运输在生理谷胱甘肽水平下形成的Fe-GSH复合物,表明其在调节不稳定铁池和降低细胞内铁毒性中的作用。这些发现强调了转运体-螯合剂相互作用在形成耐药性和敏感性中的重要性,并强调了ABC转运体在调节螯合剂活性中的复杂作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ABCC1 promotes GSH-dependent iron transport and resistance to Fe(II) and Cu(II) chelators.

Therapy resistance is a major challenge in cancer treatment, with multidrug resistance (MDR) being a well-characterized phenomenon wherein cancer cells develop resistance not only to the administered drug but also to structurally diverse compounds. Metal chelators, including quinolines and thiosemicarbazones, have shown broad antitumor activity and potential in overcoming MDR by modulating metal metabolism. However, predicting whether chelators increase or decrease toxicity in MDR cells remains complex, especially as chelator-metal complexes may become substrates for ATP-binding cassette (ABC) transporters, leading to resistance or hypersensitivity. In this study, we developed cell lines with comparable expression levels of the three major MDR ABC transporters (ABCB1, ABCC1, and ABCG2). Our findings demonstrated distinct transporter-specific influences on chelator toxicity. Cells expressing ABCC1 displayed significant resistance to thiosemicarbazones (Dp44mT, COTI-2, DpC) in both their metal-free and metal-bound forms. Vesicular transport assays further demonstrated that ABCC1 actively transports the Fe-GSH complex, formed under physiological glutathione levels, indicating its role in regulating the labile iron pool and reducing intracellular iron toxicity. These findings underscore the importance of transporter-chelator interactions in shaping drug resistance and sensitivity and highlight the intricate roles of ABC transporters in modulating chelator activity.

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来源期刊
Biometals
Biometals 生物-生化与分子生物学
CiteScore
5.90
自引率
8.60%
发文量
111
审稿时长
3 months
期刊介绍: BioMetals is the only established journal to feature the important role of metal ions in chemistry, biology, biochemistry, environmental science, and medicine. BioMetals is an international, multidisciplinary journal singularly devoted to the rapid publication of the fundamental advances of both basic and applied research in this field. BioMetals offers a forum for innovative research and clinical results on the structure and function of: - metal ions - metal chelates, - siderophores, - metal-containing proteins - biominerals in all biosystems. - BioMetals rapidly publishes original articles and reviews. BioMetals is a journal for metals researchers who practice in medicine, biochemistry, pharmacology, toxicology, microbiology, cell biology, chemistry, and plant physiology who are based academic, industrial and government laboratories.
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