4.7 Article

Induction of apoptosis by quercetin is mediated through AMPKα1/ASK1/p38 pathway

Journal

CANCER LETTERS
Volume 292, Issue 2, Pages 228-236

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2009.12.005

Keywords

ROS; Quercetin; ASK1; AMPK alpha 1; Apoptosis

Categories

Funding

  1. Korea government (MEST) [R01-2008-000-20131-0]
  2. National Research Foundation of Korea [2008-0061155, R01-2008-000-20131-0, 2005-2000377] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Effective strategies for cancer prevention and treatment can be identified by understanding the mechanism of apoptotic pathways. In this study, we investigated the regulatory mechanism of quercetin-induced apoptosis through apoptosis signal-regulating kinase (ASK)-1 and mitogen-activated protein kinase pathways Our results showed that quercetin increased apoptotic cell death through reactive oxygen species (ROS) generation and was responsible for ASK1 activation. Increasing ASK1 activity was accompanied by p38 activation Interestingly, AMP-activated protein kinase (AMPK) seemed to be a critical controller of quercetin-regulated ASK1/p38 activation. Blocking AMPK alpha 1 activity using Compound C, a synthetic inhibitor or siRNA showed that quercetin-activated ASK1 could not stimulate p38 activity. Thus, we suggested that quercetin-exerted apoptotic effects involve ROS/AMPK alpha 1/ASK1/p38 signaling pathway, and AMPK alpha 1 is a necessary element for apoptotic event induced by ASK1 (C) 2009 Elsevier Ireland Ltd All rights reserved.

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