Suppr超能文献

吩噻嗪类药物的治疗机制:癌症治疗与抗生素耐药性进展的小型综述

Therapeutic Mechanisms of Phenothiazine Drugs: A Mini-Review of Advances in Cancer Treatment and Antibiotic Resistance.

作者信息

Zou Xuewei, Xie Bai

机构信息

College of Veterinary Medicine of Yangzhou University, Yangzhou, China.

出版信息

Iran J Pharm Res. 2025 Feb 8;24(1):e157923. doi: 10.5812/ijpr-157923. eCollection 2025 Jan-Dec.

Abstract

CONTEXT

Cancer and antibiotic resistance are critical global health challenges. Phenothiazines, initially developed as antipsychotics, have demonstrated diverse biological activities, including antitumor, antibacterial, and antioxidant effects. Advances in phenothiazine synthesis have produced derivatives with broader therapeutic potential by modulating receptors, ion channels, and inducing lysosomal cell death. This review explores the therapeutic potential of phenothiazines in oncology and infectious disease management, focusing on their mechanisms of action and future clinical applications.

EVIDENCE ACQUISITION

This narrative review synthesizes insights from relevant preclinical studies on phenothiazines' applications in oncology and infectious diseases. Mechanistic pathways and experimental outcomes were analyzed to highlight therapeutic potentials and limitations.

RESULTS

Phenothiazines demonstrate significant potential in oncology by inhibiting tumor growth via apoptosis induction, pathway modulation (e.g., PDK1/Akt, MAPK/ERK1/2, and Akt/mTOR), angiogenesis suppression through vascular endothelial growth factor (VEGF) production inhibition, and enhancing the effectiveness of monoclonal antibody therapies. They disrupt key cancer-promoting pathways and induce lysosomal cell death. Beyond oncology, phenothiazines exhibit antibacterial activity, targeting efflux pumps (Eps) and restoring antibiotic susceptibility in multidrug-resistant (MDR) pathogens. These multifaceted actions position phenothiazines as promising agents for combination therapies in cancer treatment and antibiotic-resistant infections.

CONCLUSIONS

Phenothiazines hold promise as adjuvants in cancer and antibiotic resistance management. Further research should focus on optimizing their pharmacological profiles, elucidating molecular mechanisms, and validating their efficacy through clinical trials.

摘要

背景

癌症和抗生素耐药性是全球面临的重大健康挑战。吩噻嗪最初作为抗精神病药物开发,已显示出多种生物活性,包括抗肿瘤、抗菌和抗氧化作用。吩噻嗪合成技术的进步通过调节受体、离子通道和诱导溶酶体细胞死亡,产生了具有更广泛治疗潜力的衍生物。本综述探讨了吩噻嗪在肿瘤学和传染病管理中的治疗潜力,重点关注其作用机制和未来的临床应用。

证据获取

本叙述性综述综合了有关吩噻嗪在肿瘤学和传染病应用的相关临床前研究的见解。分析了作用机制途径和实验结果,以突出治疗潜力和局限性。

结果

吩噻嗪在肿瘤学方面具有显著潜力,可通过诱导凋亡抑制肿瘤生长、调节信号通路(如PDK1/Akt、MAPK/ERK1/2和Akt/mTOR)、抑制血管内皮生长因子(VEGF)产生来抑制血管生成以及增强单克隆抗体疗法的有效性。它们破坏关键的促癌途径并诱导溶酶体细胞死亡。除肿瘤学外,吩噻嗪还具有抗菌活性,可靶向外排泵(Eps)并恢复多重耐药(MDR)病原体的抗生素敏感性。这些多方面的作用使吩噻嗪成为癌症治疗和抗生素耐药感染联合治疗的有前景的药物。

结论

吩噻嗪有望作为癌症和抗生素耐药性管理的佐剂。进一步的研究应集中在优化其药理学特性、阐明分子机制以及通过临床试验验证其疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcee/12297022/6704aefcbd39/ijpr-24-1-157923-i001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验