硝唑啉在泌尿系统肿瘤学中的应用--证据综述

W. Tomczak, Wojciech Krajewski, Joanna Chorbińska, Ł. Nowak, J. Łaszkiewicz, Katarzyna Grunwald, Adam Chełmoński, Szymon Pisarski, T. Szydełko
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引用次数: 0

摘要

泌尿系统癌症的发病率和死亡率居高不下,凸显了对有效、安全治疗的迫切需求。传统的化疗方案往往受限于高毒性、癌症的耐药性以及管理独立发展的多灶扩散所带来的挑战。在这种情况下,再利用战略就显得尤为诱人。它可以引入一种已知安全性的药物,从而大大减少引入新疗法所需的成本和时间。硝唑啉(NIT)是一种药代动力学特征成熟的药物,已有 50 多年的历史,常用于治疗无并发症的尿路感染,最近因其潜在的肿瘤学应用而备受关注。鉴于 NIT 的药代动力学特性,我们特别关注其排泄特征最有利的泌尿系统癌症。我们研究了所有可用的研究,结果表明 NIT 在抑制血管生成、组织侵袭、转移形成和对抗多药耐药性方面具有显著效果。我们发现,NIT 的功效和作用机制在不同的细胞系中各不相同。迄今为止的研究结果很有希望,表明 NIT 或其衍生物可在肿瘤学中发挥作用,但要充分了解其在癌症治疗中的潜力和适用性,还需要进一步的研究。
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Application of nitroxoline in urologic oncology – a review of evidence
The persistence of high incidence and mortality rates associated with urologic cancers underscores the urgent need for effective and safe treatments. Conventional chemotherapy regimens are often limited by their high toxicity, the cancer’s drug resistance, and the challenge of managing independently evolving multifocal spread. In this context, a repurposing strategy is particularly enticing. It allows for the introduction of a drug with a known safety profile, thus significantly reducing the costs and time necessary to introduce a new treatment. Nitroxoline (NIT), a drug with a well-established pharmacokinetic profile known for over 50 years and utilised in treating uncomplicated urinary tract infections, has recently garnered attention for its potential oncologic applications. Given the pharmacokinetic properties of NIT, our focus was specifically on urologic cancers in which its excretion profile is most advantageous. We examined all available studies, demonstrating significant effectiveness of NIT in inhibiting angiogenesis, tissue invasion, metastasis formation, and counteracting multidrug resistance. The efficacy and mechanism of action of NIT were found to vary across different cell lines. The findings to date are promising, suggesting that NIT or its derivatives could play a role in oncology, although further research is necessary to fully understand its potential and applicability in cancer treatment.
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