Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan.
Department of Postgraduate Education and Research, Kazakhstan Medical University KSPH, Almaty, Kazakhstan.
Gene. 2020 May 5;737:144452. doi: 10.1016/j.gene.2020.144452. Epub 2020 Feb 7.
There has always been a quest to search for synthetic and natural compounds having premium pharmacological properties and minimum off-target and/or side effects. Therefore, in accordance with this approach, scientists have given special attention to the molecules having remarkable ability to target oncogenic protein network, restore drug sensitivity and induce apoptosis in cancer cells. The mechanisms through which general anesthetics modulated wide-ranging deregulated cell signaling pathways and non-coding RNAs remained unclear. However, rapidly accumulating experimentally verified evidence has started to resolve this long-standing mystery and a knowledge about these important molecular targets has surfaced and how these drugs act at the molecular level is becoming more understandable. In this review we have given special attention to available evidence related to ability of propofol to modulate Wnt/β-catenin, JAK/STAT and mTOR-driven pathway. Excitingly, great strides have been made in sharpening our concepts related to potential of propofol to modulate non-coding RNAs in different cancers. Collectively, these latest findings offer interesting, unexplored opportunities to target deregulated signaling pathways to induce apoptosis in drug-resistant cancers.
一直以来,人们都在寻找具有优质药理特性、最小脱靶和/或副作用的合成和天然化合物。因此,根据这一方法,科学家们特别关注那些具有显著靶向致癌蛋白网络、恢复药物敏感性和诱导癌细胞凋亡能力的分子。然而,一般麻醉剂调节广泛失调的细胞信号通路和非编码 RNA 的机制尚不清楚。然而,迅速积累的实验验证证据开始解决这个长期存在的谜团,关于这些重要分子靶点的知识已经浮出水面,这些药物在分子水平上的作用方式也变得更加容易理解。在这篇综述中,我们特别关注了与异丙酚调节 Wnt/β-catenin、JAK/STAT 和 mTOR 驱动途径的能力相关的现有证据。令人兴奋的是,在锐化我们关于异丙酚调节不同癌症中非编码 RNA 的潜力的概念方面已经取得了重大进展。总的来说,这些最新发现为靶向失调的信号通路提供了有趣的、尚未探索的机会,以诱导耐药性癌症中的细胞凋亡。