Muhammad Farrukh Nisar, Chunpeng Wan, Dietrich Büsselberg, Daniela Calina, Javad Sharifi-Rad
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引用次数: 0
Abstract
Cancer remains a global health challenge, with drug resistance and disease recurrence posing significant obstacles despite advances in immunotherapy and targeted treatments. This has driven interest in natural products as sources of novel anticancer agents. Withania somnifera (Ashwagandha), a well-regarded plant in Ayurvedic medicine, is noted for its various therapeutic properties, including anticancer effects. Among its bioactive compounds, Withaferin A (WFA), a steroidal lactone, has shown notable promise in reducing inflammation, angiogenesis, and tumor proliferation with minimal toxicity. This review examines the anticancer properties of WFA, with a focus on its mechanisms of action, therapeutic efficacy, and safety profile across various cancer types. A comprehensive literature review was conducted, compiling data from in vitro and in vivo studies that investigate WFA's impact on cancer hallmarks, including apoptosis induction, angiogenesis reduction, and metastasis inhibition. Key molecular interactions with NFκB, STAT, HSP90, estrogen receptors, p53, and TGFβ pathways are highlighted. Findings indicate that WFA exhibits significant anticancer activity by modulating critical signaling pathways and inducing apoptosis with minimal adverse effects. In preclinical models, WFA demonstrated therapeutic potential across multiple cancers, such as breast, colon, prostate, ovarian, lung, and brain cancers. WFA represents a promising candidate for future cancer therapies, particularly as a natural adjuvant that could enhance treatment efficacy with low toxicity. Further clinical trials are needed to explore WFA's full potential and confirm its safety in human oncology.
癌症仍然是一个全球性的健康挑战,尽管免疫疗法和靶向治疗取得了进展,但耐药性和疾病复发构成了重大障碍。这引起了人们对天然产品作为新型抗癌剂来源的兴趣。Withania somnifera (Ashwagandha)是印度草药中备受推崇的植物,以其各种治疗特性而闻名,包括抗癌作用。在其生物活性化合物中,Withaferin A (WFA)是一种甾体内酯,在减少炎症、血管生成和肿瘤增殖方面具有显著的前景,而且毒性很小。本文综述了WFA的抗癌特性,重点介绍了WFA在不同癌症类型中的作用机制、治疗效果和安全性。我们进行了全面的文献综述,收集了来自体外和体内研究的数据,研究了WFA对癌症特征的影响,包括诱导细胞凋亡、减少血管生成和抑制转移。强调了与NFκB、STAT、HSP90、雌激素受体、p53和TGFβ通路的关键分子相互作用。研究结果表明,WFA通过调节关键信号通路和诱导细胞凋亡而具有显著的抗癌活性,而不良反应最小。在临床前模型中,WFA显示出对多种癌症的治疗潜力,如乳腺癌、结肠癌、前列腺癌、卵巢癌、肺癌和脑癌。WFA代表了未来癌症治疗的一个有希望的候选者,特别是作为一种天然佐剂,可以提高低毒性的治疗效果。需要进一步的临床试验来探索WFA的全部潜力并确认其在人类肿瘤中的安全性。
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.