用已获批准的药物抑制线粒体功能可克服鼻咽癌的化疗耐药性。

IF 1.8 4区 医学 Q3 ONCOLOGY
Anti-Cancer Drugs Pub Date : 2024-04-01 Epub Date: 2024-01-15 DOI:10.1097/CAD.0000000000001566
Yunlong Zhang, Difeng Guo, Yongbo Zhu, Lin Liu
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引用次数: 0

摘要

鼻咽癌(NPC)的化疗耐药性是一项重大的治疗挑战,而其潜在机制仍不甚明了。在之前的研究中,我们强调了异戊二烯半胱氨酸羧基甲基转移酶(ICMT)与鼻咽癌化疗耐药性之间的关联。在目前的研究中,我们发现对 5-FU 和顺铂耐药的鼻咽癌细胞均表现出线粒体功能增强和线粒体基因表达增加,这与 ICMT 无关。我们的研究进一步表明,与亲代细胞相比,传统的线粒体抑制剂(如寡霉素、抗霉素和鱼藤酮)在降低化疗耐药鼻咽癌细胞的存活率方面更为有效。此外,我们还发现了两种抗菌药物--替加环素和阿托伐醌,它们被认为是线粒体抑制剂,是通过靶向线粒体呼吸减少化疗耐药鼻咽癌细胞的有效药物。值得注意的是,在小鼠模型中,以可耐受的剂量给药的替加环素和阿托伐醌可抑制化疗耐药的鼻咽癌细胞生长,并延长总存活率。这项研究揭示了线粒体抑制作为克服鼻咽癌化疗耐药性的有效策略的前景。此外,我们的研究结果还强调了将替加环素和阿托伐醌等临床可用药物重新用于治疗出现化疗耐药性的鼻咽癌患者的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of mitochondrial function by approved drugs overcomes nasopharyngeal carcinoma chemoresistance.

The development of chemo-resistance in nasopharyngeal carcinoma (NPC) presents a significant therapeutic challenge, and its underlying mechanisms remain poorly understood. In our previous studies, we highlighted the association between isoprenylcysteine carboxylmethyltransferase (ICMT) and chemoresistance in NPC. In this current research, we revealed that both 5-FU and cisplatin-resistant NPC cells exhibited elevated mitochondrial function and increased expression of mitochondrial genes, independent of ICMT. Our investigations further showed that classic mitochondrial inhibitors, such as oligomycin, antimycin, and rotenone, were notably more effective in reducing viability in chemo-resistant NPC cells compared to parental cells. Moreover, we identified two antimicrobial drugs, tigecycline and atovaquone, recognized as mitochondrial inhibitors, as potent agents for decreasing chemo-resistant NPC cells by targeting mitochondrial respiration. Remarkably, tigecycline and atovaquone, administered at tolerable doses, inhibited chemo-resistant NPC growth in mouse models and extended overall survival rates. This work unveils the efficacy of mitochondrial inhibition as a promising strategy to overcome chemo-resistance in NPC. Additionally, our findings highlight the potential repurposing of clinically available drugs like tigecycline and atovaquone for treating NPC patients who develop chemoresistance.

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来源期刊
Anti-Cancer Drugs
Anti-Cancer Drugs 医学-药学
CiteScore
3.80
自引率
0.00%
发文量
244
审稿时长
3 months
期刊介绍: Anti-Cancer Drugs reports both clinical and experimental results related to anti-cancer drugs, and welcomes contributions on anti-cancer drug design, drug delivery, pharmacology, hormonal and biological modalities and chemotherapy evaluation. An internationally refereed journal devoted to the fast publication of innovative investigations on therapeutic agents against cancer, Anti-Cancer Drugs aims to stimulate and report research on both toxic and non-toxic anti-cancer agents. Consequently, the scope on the journal will cover both conventional cytotoxic chemotherapy and hormonal or biological response modalities such as interleukins and immunotherapy. Submitted articles undergo a preliminary review by the editor. Some articles may be returned to authors without further consideration. Those being considered for publication will undergo further assessment and peer-review by the editors and those invited to do so from a reviewer pool.
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