Plant-derived terpenoids modulating cancer cell metabolism and cross-linked signaling pathways: an updated reviews.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-07-01 Epub Date: 2025-02-28 DOI:10.1007/s00210-025-03937-y
Pratibha Pandey, Meenakshi Verma, Gaurav Sanghvi, Roopashree R, Kamal Kant Joshi, Kavitha V, Subhashree Ray, Seema Ramniwas, Ajay Singh, Sorabh Lakhanpal, Fahad Khan
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Abstract

Cancer is a critical health issue that remains a predominant cause of mortality globally. It is a complex disease that may effectively regulate many signaling pathways and modify the metabolism of the body to evade the immune system. Understanding neoplastic metabolic reprogramming as a hallmark of cancer has facilitated the creation of innovative metabolism-targeted treatment strategies. Various signaling cascades, such as the PI3K/Akt/mTOR, ERK, JAK/STAT, MAPK/p38, NF-κB/Nrf2, and apoptotic pathways, are commonly involved in this process. It is now widely recognized that an inadequate response and the subsequent development of resistance are frequently caused by the highly selective blockage of these pathways in tumor cells. Consequently, to enhance the overall efficacy of anticancer agents, it is crucial to employ multi-target compounds that can concurrently inhibit multiple vital processes within tumor cells. The utilization of plant-derived bioactive compounds for this purpose is particularly promising, owing to their varied structures and numerous targets. Among these bioactive compounds, terpenoids have exhibited significant anticancer efficacy by targeting various altered signaling pathways. Thus, this review examines the terpenoid class of plant-derived compounds exhibiting potential anticancer activity, including their impact on metabolism and interconnected deregulated signaling pathways in human tumor cells. Accordingly, current research will help in the rational design and critical evaluation of innovative anticancer therapeutics utilizing plant-derived terpenoids for the modulation of cross-linked signaling pathways of cancer metabolism.

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植物源萜类调节癌细胞代谢和交联信号通路:最新综述。
癌症是一个严重的健康问题,仍然是全球死亡的主要原因。它是一种复杂的疾病,可以有效地调节许多信号通路,改变身体的代谢,以逃避免疫系统。了解肿瘤代谢重编程作为癌症的标志,促进了创新代谢靶向治疗策略的创建。PI3K/Akt/mTOR、ERK、JAK/STAT、MAPK/p38、NF-κB/Nrf2和凋亡通路等信号级联通常参与这一过程。现在人们普遍认识到,不充分的反应和随后的耐药性的发展往往是由肿瘤细胞中这些途径的高度选择性阻断引起的。因此,为了提高抗癌药物的整体疗效,使用能够同时抑制肿瘤细胞内多个重要过程的多靶点化合物是至关重要的。利用植物源性生物活性化合物用于这一目的是特别有希望的,因为它们的结构多样,靶点众多。在这些生物活性化合物中,萜类化合物通过靶向各种改变的信号通路而显示出显著的抗癌功效。因此,本文综述了萜类植物源化合物具有潜在的抗癌活性,包括它们对人类肿瘤细胞代谢和相互关联的信号通路的影响。因此,目前的研究将有助于合理设计和批判性评估利用植物源萜类化合物调节癌症代谢交联信号通路的创新抗癌治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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