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vernolide-A 和 vernodaline:具有细胞毒性的倍半萜内酯类化合物,可对抗癌症。

Vernolide-A and Vernodaline: Sesquiterpene Lactones with Cytotoxicity against Cancer.

机构信息

Faculty of Biotechnology, Ho Chi Minh City Open University, Ho Chi Minh City, Vietnam.

NTT Hi-Tech Institute, Nguyen Tat Thanh University, Ho Chi Minh City, Vietnam.

出版信息

J Environ Pathol Toxicol Oncol. 2020;39(4):299-308. doi: 10.1615/JEnvironPatholToxicolOncol.2020034066.

Abstract

Vernolide-A and vernodaline are sesquiterpene lactones isolated from genera of Vernonia. Vernolide-A and vernodaline have shown promising therapeutic properties, including antibacterial, antihelminth, and antioxidant activities. Recently, the anticancer properties of these sesquiterpene lactones have been investigated with the elucidation of effects on cell proliferation, metastasis, angiogenesis, and apoptosis. The antiproliferation and antimetastatic activities arise from targeting extracellular signal-regulated kinase 1 (ERK-1), extracellular signal-regulated kinase 2 (ERK-2), nuclear factor-κB (NF-κB), signal transducer and activator of transcription 3 (STAT3), matrix metalloproteinase 2 (MMP-2), and matrix metalloproteinase 9 (MMP9). The induction of apoptosis is due to the enhancement of caspase 9, caspase 3, while inhibition of Bcl-2 and Bcl-xL results in the release of cytochrome c into the cytosol. The activity of vernolide-A and vernodaline is hypothesized to be due to thiol reactivity through the α-methylene-γ-lactone group of sesquiterpene lactones. This review will give a brief summary of the anticancer activity of vernolide-A and vernodaline and provide information on the underlying molecular mechanisms.

摘要

紫堇灵 A 和紫堇达明是从 Vernonia 属植物中分离得到的倍半萜内酯。紫堇灵 A 和紫堇达明具有有前景的治疗特性,包括抗菌、抗蠕虫和抗氧化活性。最近,这些倍半萜内酯的抗癌特性已通过研究其对细胞增殖、转移、血管生成和细胞凋亡的影响得到了阐明。其具有的增殖抑制和抗转移活性源于靶向细胞外信号调节激酶 1(ERK-1)、细胞外信号调节激酶 2(ERK-2)、核因子-κB(NF-κB)、信号转导和转录激活因子 3(STAT3)、基质金属蛋白酶 2(MMP-2)和基质金属蛋白酶 9(MMP9)。诱导细胞凋亡是由于增强了半胱天冬酶 9、半胱天冬酶 3,同时抑制 Bcl-2 和 Bcl-xL 导致细胞色素 c 释放到细胞质中。紫堇灵 A 和紫堇达明的活性被假设是由于通过倍半萜内酯的α-亚甲基-γ-内酯基团的硫醇反应性。本综述将简要总结紫堇灵 A 和紫堇达明的抗癌活性,并提供有关潜在分子机制的信息。

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