Signaling pathways behind the biological effects of tanshinone IIA for the prevention of cancer and cardiovascular diseases.

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY Naunyn-Schmiedeberg's archives of pharmacology Pub Date : 2025-07-01 Epub Date: 2025-02-12 DOI:10.1007/s00210-025-03857-x
Homa Shahrokhi, Javad Asili, Zahra Tayarani-Najaran, Motahareh Boozari
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Abstract

Tanshinone IIA (Tan IIA) is a well-known fat-soluble diterpenoid found in Salvia miltiorrhiza, recognized for its various biological effects. The molecular signaling pathways of Tan IIA have been investigated in different diseases, including the anti-inflammatory, hepatoprotective, renoprotective, neuroprotective effects, and fibrosis prevention. This article provides a brief overview of the signaling pathways related to anti-cancer and cardioprotective effects of Tan IIA. It shows that Tan IIAs anti-cancer ability has good expectation through multiplicity mechanisms affecting various aspects' tumor biology. The major pathways involved in its anti-cancer effects include inhibition of PI3/Akt, MAPK, and p53/p21 signaling which leads to enhancement of immune responses and increased radiation sensitivity. Some essential pathways responsible for cardioprotective effects induced by Tan IIA are PI3/AKT activation, MAPK, and SIRT1 promoting protection against ischemia/reperfusion injury in myocardial cells as well as inhibiting pathological remodeling processes. Finally, the article underscores the complex and specific signaling pathways influenced by Tan IIA. The PI3/Akt and MAPK pathways play critical roles in the anti-cancer and cardioprotective effects of Tan IIA. Particularly, Tan IIA suppresses the proliferation of malignancies in cancerous cells but stimulates protective mechanisms in normal cardiovascular cells. These findings highlight the importance of investigating molecular signaling pathways in evaluating the therapeutic potential of natural products. Studying about signaling pathways is vital in understanding the therapeutic aspects of Tan IIA and its derivatives as anti-cancer and cardio-protective agents. Further research is necessary to understand these complex mechanisms.

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丹参酮IIA预防癌症和心血管疾病生物学效应背后的信号通路。
丹参酮IIA (Tan IIA)是一种众所周知的脂溶性二萜类化合物,发现于丹参中,具有多种生物效应。Tan IIA的分子信号通路已在不同疾病中被研究,包括抗炎、肝保护、肾保护、神经保护和纤维化预防作用。本文就Tan IIA的抗癌和心脏保护作用的相关信号通路作一综述。说明Tan IIAs通过多种机制影响肿瘤生物学的各个方面,具有良好的抗癌能力。其抗癌作用的主要途径包括抑制PI3/Akt、MAPK和p53/p21信号通路,从而增强免疫反应和增加辐射敏感性。Tan IIA诱导心肌保护作用的一些重要途径是PI3/AKT激活、MAPK和SIRT1促进心肌细胞对缺血/再灌注损伤的保护并抑制病理性重构过程。最后,文章强调了受Tan IIA影响的复杂而特定的信号通路。PI3/Akt和MAPK通路在Tan IIA的抗癌和心脏保护作用中发挥关键作用。特别是,Tan IIA抑制癌细胞中恶性肿瘤的增殖,但刺激正常心血管细胞的保护机制。这些发现强调了研究分子信号通路在评估天然产物治疗潜力中的重要性。研究信号通路对了解Tan IIA及其衍生物作为抗癌和心脏保护剂的治疗作用至关重要。了解这些复杂的机制需要进一步的研究。
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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