NLRP3 inflammasome-based therapies by natural products: a new development in the context of cancer therapy.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-09-01 Epub Date: 2025-03-21 DOI:10.1007/s00210-025-04030-0
Hamza Abu Owida, Ahmed Yaseen Abed, Farag M A Altalbawy, Malathi H, Vikrant Abbot, Sanoeva Matlyuba Jakhonkulovna, Suleiman Ibrahim Mohammad, Asokan Vasudevan, Reem Mohsin Khalaf, Ahmed Hussein Zwamel
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Abstract

The leucine-rich repeat containing protein (NLR) canonical inflammasome family includes Nod-like receptor protein 3 (NLRP3). Via the mediation of apoptosis proteins and immunological reactions, it controls the pathogenesis of malignancy. Experimental studies showed a relationship among lymphogenesis, cancer metastasis, and NLRP3 expression. Natural products have also been used as lead-based substances in a number of investigations to speed up the creation of novel, specific NLRP3 inhibitors. Via the mediation of apoptotic proteins and immunological responses, it controls the pathogenesis of malignancy. Moreover, it was recently noted that among human cancers, chemotherapy activates NLRP3. Induction of NLRP3 could encourage the generation of IL-1β and IL-22 to facilitate the propagation of malignancy. Additionally, prior research has demonstrated that the usage of NLRP3 in cancer therapy may result in resistance to drugs. The depletion of NLRP3 could affect the survival of cells. Natural products have been used as lead materials in a number of studies to help generate novel, specific NLRP3 antagonists more quickly. In the present review, we examine the mechanism behind the beneficial effects of the natural substances on the inhibition of cancer growth and progression, with special focus on NLRP3 regulation.

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天然产物NLRP3炎性小体治疗:癌症治疗背景下的新进展
富含亮氨酸重复序列蛋白(NLR)的典型炎性小体家族包括nod样受体蛋白3 (NLRP3)。它通过介导凋亡蛋白和免疫反应,控制恶性肿瘤的发病机制。实验研究表明,NLRP3的表达与淋巴细胞发生、肿瘤转移有关。在许多研究中,天然产物也被用作铅基物质,以加速新型特异性NLRP3抑制剂的产生。它通过介导凋亡蛋白和免疫反应,控制恶性肿瘤的发病机制。此外,最近发现,在人类癌症中,化疗可激活NLRP3。诱导NLRP3可促进IL-1β和IL-22的生成,促进恶性肿瘤的增殖。此外,先前的研究表明,在癌症治疗中使用NLRP3可能会导致药物耐药。NLRP3的缺失会影响细胞的存活。在许多研究中,天然产物已被用作先导材料,以帮助更快地产生新的特异性NLRP3拮抗剂。在本综述中,我们研究了天然物质对抑制癌症生长和进展的有益作用背后的机制,特别关注NLRP3的调控。
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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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