Molecular Targets of Nimbolide for Anti-Cancer Therapy: An Updated Review.

P. Elumalai, D. Ezhilarasan, S. Raghunandhakumar
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引用次数: 1

Abstract

Cancer is a major cause of death worldwide with an increasing incidence rate and is considered a major public health problem. Distance metastasis to other tissues, high toxicity, and drug resistance of cancer cells to chemotherapy demand novel therapeutic approaches to treat cancer. Natural compounds from medicinal plants have been studied for therapeutic use in various malignancies. Nimbolide is an active principal compound from Azadirachta indica, which is an Asian traditional medicinal plant utilized historically as a remedy for a variety of diseases due to its antioxidant, anti-inflammatory, anti-cancer, and antimicrobial properties. It is a limonoid triterpene possessing potent anti-cancer effects in various types of cancers. It has been reported to induce multiple cytotoxic effects in tumor cells by modulating the cell proliferation, cell cycle, apoptosis, and metastasis by altering the various molecular signaling pathways. In the present review, we summarized all the in vitro and in vivo studies reporting the molecular targets of nimbolide for the therapeutic approaches in different types of cancer cells. We analyzed research publications up to September 2021 on the effect of nimbolide in various malignancies and the molecular mechanism of action. Nimbolide targets different signaling pathways including epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), insulin like growth factor (IGF), Wingless and INT-1 (Wnt)/β-catenin, mitogen-activated protein kinases (MAPK)/c-Jun N-terminal kinases (JNK), phosphoinositide 3-kinase (PI3K)/AKT, tumor necrosis factor-α (TNF-α)/nuclear factor kappa B (NF-κβ), and death receptor 5 (DR5) in several cancer cells. Nimbolide's widespread availability and absence of side effects, as well as understanding the molecular mechanism of nimbolide's action, will be useful to develop a therapeutic agent against cancer.
Nimbolide用于抗癌治疗的分子靶点:最新综述。
癌症是全世界死亡的主要原因,发病率不断上升,被认为是一个主要的公共卫生问题。肿瘤细胞的远距离转移、高毒性以及对化疗的耐药等特点需要新的治疗方法。从药用植物中提取的天然化合物已被研究用于治疗各种恶性肿瘤。Nimbolide是一种来自印楝的活性主要化合物,印楝是一种亚洲传统药用植物,由于其抗氧化、抗炎、抗癌和抗菌特性,在历史上被用作治疗多种疾病的药物。它是一种类柠檬三萜,对各种类型的癌症具有有效的抗癌作用。据报道,它通过改变多种分子信号通路,调节细胞增殖、细胞周期、凋亡和转移,从而诱导肿瘤细胞的多种细胞毒性作用。在本文中,我们对nimbolide在不同类型癌细胞治疗方法中的分子靶点进行了综述。我们分析了截至2021年9月关于nimbolide在各种恶性肿瘤中的作用和分子作用机制的研究出版物。Nimbolide靶向多种肿瘤细胞中不同的信号通路,包括表皮生长因子(EGF)、血管内皮生长因子(VEGF)、胰岛素样生长因子(IGF)、无翼和INT-1 (Wnt)/β-catenin、丝裂原活化蛋白激酶(MAPK)/c-Jun n-末端激酶(JNK)、磷酸肌肽3-激酶(PI3K)/AKT、肿瘤坏死因子-α (TNF-α)/核因子κ B (NF-κβ)和死亡受体5 (DR5)。Nimbolide的广泛可用性和无副作用,以及了解Nimbolide作用的分子机制,将有助于开发抗癌药物。
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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