Park Dohyun, Jeong Heeyoon, Lee Mi Nam, Koh Ara, Kwon Ohman, Yang Yong Ryoul, Noh Jungeun, Suh Pann-Ghill, Park Hwangseo, Ryu Sung Ho
Department of Life Sciences, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea.
School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea.
Sci Rep. 2016 Feb 23;6:21772. doi: 10.1038/srep21772.
Resveratrol (RSV) is a natural polyphenol that has a beneficial effect on health, and resveratrol-induced autophagy has been suggested to be a key process in mediating many beneficial effects of resveratrol, such as reduction of inflammation and induction of cancer cell death. Although various resveratrol targets have been suggested, the molecule that mediates resveratrol-induced autophagy remains unknown. Here, we demonstrate that resveratrol induces autophagy by directly inhibiting the mTOR-ULK1 pathway. We found that inhibition of mTOR activity and presence of ULK1 are required for autophagy induction by resveratrol. In line with this mTOR dependency, we found that resveratrol suppresses the viability of MCF7 cells but not of SW620 cells, which are mTOR inhibitor sensitive and insensitive cancer cells, respectively. We also found that resveratrol-induced cancer cell suppression occurred ULK1 dependently. For the mechanism of action of resveratrol on mTOR inhibition, we demonstrate that resveratrol directly inhibits mTOR. We found that resveratrol inhibits mTOR by docking onto the ATP-binding pocket of mTOR (i.e., it competes with ATP). We propose mTOR as a novel direct target of resveratrol, and inhibition of mTOR is necessary for autophagy induction.
白藜芦醇(RSV)是一种对健康有益的天然多酚,白藜芦醇诱导的自噬被认为是介导白藜芦醇许多有益作用的关键过程,如减轻炎症和诱导癌细胞死亡。尽管已经提出了各种白藜芦醇靶点,但介导白藜芦醇诱导自噬的分子仍然未知。在这里,我们证明白藜芦醇通过直接抑制mTOR-ULK1途径诱导自噬。我们发现,抑制mTOR活性和存在ULK1是白藜芦醇诱导自噬所必需的。与这种对mTOR的依赖性一致,我们发现白藜芦醇抑制MCF7细胞的活力,但不抑制SW620细胞的活力,这两种细胞分别是对mTOR抑制剂敏感和不敏感的癌细胞。我们还发现白藜芦醇诱导的癌细胞抑制作用依赖于ULK1。关于白藜芦醇对mTOR抑制的作用机制,我们证明白藜芦醇直接抑制mTOR。我们发现白藜芦醇通过对接至mTOR的ATP结合口袋来抑制mTOR(即,它与ATP竞争)。我们提出mTOR是白藜芦醇的一个新的直接靶点,抑制mTOR是诱导自噬所必需的。