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Plant natural compounds: Targeting pathways of autophagy as anti-cancer therapeutic agents

机译:植物天然化合物:自噬作为抗癌治疗剂的靶向途径

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Natural compounds derived from plant sources are well characterized as possessing a wide variety of remarkable anti-tumour properties, for example modulating programmed cell death, primarily referring to apoptosis, and autophagy. Distinct from apoptosis, autophagy (an evolutionarily conserved, multi-step lysosomal degradation process in which a cell destroys long-lived proteins and damaged organelles) may play crucial regulatory roles in many pathological processes, most notably in cancer. In this review, we focus on highlighting several representative plant natural compounds such as curcumin, resveratrol, paclitaxel, oridonin, quercetin and plant lectin - that may lead to cancer cell death - for regulation of some core autophagic pathways, involved in Ras-Raf signalling, Beclin-1 interactome, BCR-ABL, PI3KCI/Akt/mTOR, FOXO1 signalling and p53. Taken together, these findings would provide a new perspective for exploiting more plant natural compounds as potential novel anti-tumour drugs, by targeting the pathways of autophagy, for future cancer therapeutics.
机译:来自植物来源的天然化合物被很好地表征为具有多种显着的抗肿瘤特性,例如调节程序性细胞死亡,主要是指细胞凋亡和自噬。自噬不同于细胞凋亡,自噬(一种进化上保守的多步溶酶体降解过程,其中细胞破坏了长寿蛋白和受损的细胞器)可能在许多病理过程中起着至关重要的调节作用,尤其是在癌症中。在这篇综述中,我们重点介绍几种有代表性的植物天然化合物,例如姜黄素,白藜芦醇,紫杉醇,冬凌草甲素,槲皮素和植物凝集素-可能导致癌细胞死亡-调控涉及Ras-Raf信号传导的某些核心自噬途径,Beclin-1相互作用基因组,BCR-ABL,PI3KCI / Akt / mTOR,FOXO1信号传导和p53。综上所述,这些发现将为通过靶向自噬途径开发更多的植物天然化合物作为潜在的新型抗肿瘤药物提供新的前景,以用于未来的癌症治疗。

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