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艾瑞辛A抑制的关键肿瘤学通路:其作为抗癌分子开发的前景

Key oncologic pathways inhibited by Erinacine A: A perspective for its development as an anticancer molecule.

作者信息

Prasher Parteek, Sharma Mousmee, Sharma Amit Kumar, Sharifi-Rad Javad, Calina Daniela, Hano Christophe, Cho William C

机构信息

Department of Chemistry, University of Petroleum & Energy Studies, Energy Acres, Dehradun 248007, India.

Department of Chemistry, Uttaranchal University, Arcadia Grant, Dehradun 248007, India.

出版信息

Biomed Pharmacother. 2023 Apr;160:114332. doi: 10.1016/j.biopha.2023.114332. Epub 2023 Feb 1.

Abstract

In the modern era, cancer can be controlled by chemotherapy treatment, and in many situations a stable disease is obtained. The significant clinical success and subsequent commercialization of naturally derived molecules have further encouraged their exploration as adjunctive therapies in cancer management. The purpose of this comprehensive review is to update the anticancer mechanisms triggered by Erinacine A and regulation of signaling pathways potentially involved in its anticancer activity.The results of preclinical research showed that Erinacin A, a therapeutically important biological metabolite isolated from the basidiomycete fungus Hericium erinaceus offers a multitude of possible chemotherapeutic applications by regulating complex signaling pathways as validated by various pharmacological in vitro and in vivo studies. As a result of Erinacin A's action on oncological signaling pathways, it resulted in induction of apoptosis, reduction of proliferation, invasiveness, generation of oxidative stress and cell cycle arrest in cancer cells.

摘要

在现代,癌症可以通过化疗得到控制,并且在许多情况下能实现疾病稳定。天然衍生分子取得的显著临床成功及其随后的商业化进一步促使人们将其作为癌症治疗的辅助疗法进行探索。本综述的目的是更新由艾瑞尼辛A触发的抗癌机制以及可能参与其抗癌活性的信号通路调控。临床前研究结果表明,艾瑞尼辛A是从担子菌猴头菇中分离出的一种具有重要治疗意义的生物代谢产物,通过调节复杂的信号通路展现出多种可能的化疗应用,这已得到各种体外和体内药理学研究的验证。由于艾瑞尼辛A对肿瘤信号通路的作用,它导致癌细胞凋亡诱导、增殖减少、侵袭性降低、氧化应激产生以及细胞周期停滞。

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