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7-O-geranylquercetin-induced autophagy contributes to apoptosis via ROS generation in human non-small cell lung cancer cells.

Identifieur interne : 000162 ( PubMed/Corpus ); précédent : 000161; suivant : 000163

7-O-geranylquercetin-induced autophagy contributes to apoptosis via ROS generation in human non-small cell lung cancer cells.

Auteurs : En-Xia Wang ; Bo-Yang Zou ; Lei Shi ; Lin-Ying Du ; Yan-Yan Zhu ; Ya-Meng Jiang ; Xiao-Dong Ma ; Xiao-Hui Kang ; Chang-Yuan Wang ; Yu-Hong Zhen ; Li-Dan Sun

Source :

RBID : pubmed:28495516

English descriptors

Abstract

To investigate the antitumor effects of 7-O-geranylquercetin (GQ), a novel O-alkylated derivative of quercetin, against non-small cell lung cancer (NSCLC) cell lines A549 and NCI-H1975 and the corresponding mechanisms.

DOI: 10.1016/j.lfs.2017.05.008
PubMed: 28495516

Links to Exploration step

pubmed:28495516

Le document en format XML

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<term>Antineoplastic Agents (pharmacology)</term>
<term>Apoptosis (drug effects)</term>
<term>Autophagy (drug effects)</term>
<term>Carcinoma, Non-Small-Cell Lung (drug therapy)</term>
<term>Carcinoma, Non-Small-Cell Lung (pathology)</term>
<term>Cell Line</term>
<term>Cell Line, Tumor</term>
<term>Cell Survival (drug effects)</term>
<term>Dose-Response Relationship, Drug</term>
<term>Fibroblasts (drug effects)</term>
<term>Fibroblasts (metabolism)</term>
<term>Flow Cytometry</term>
<term>Gene Expression Regulation, Neoplastic (drug effects)</term>
<term>Humans</term>
<term>Lung Neoplasms (drug therapy)</term>
<term>Lung Neoplasms (pathology)</term>
<term>Microscopy, Electron, Transmission</term>
<term>Quercetin (analogs & derivatives)</term>
<term>Quercetin (pharmacology)</term>
<term>Reactive Oxygen Species (metabolism)</term>
<term>Time Factors</term>
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<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en">
<term>Quercetin</term>
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<term>Reactive Oxygen Species</term>
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<term>Antineoplastic Agents</term>
<term>Quercetin</term>
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<term>Autophagy</term>
<term>Cell Survival</term>
<term>Fibroblasts</term>
<term>Gene Expression Regulation, Neoplastic</term>
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<term>Carcinoma, Non-Small-Cell Lung</term>
<term>Lung Neoplasms</term>
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<term>Fibroblasts</term>
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<term>Carcinoma, Non-Small-Cell Lung</term>
<term>Lung Neoplasms</term>
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<term>Cell Line, Tumor</term>
<term>Dose-Response Relationship, Drug</term>
<term>Flow Cytometry</term>
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<front>
<div type="abstract" xml:lang="en">To investigate the antitumor effects of 7-O-geranylquercetin (GQ), a novel O-alkylated derivative of quercetin, against non-small cell lung cancer (NSCLC) cell lines A549 and NCI-H1975 and the corresponding mechanisms.</div>
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<Day>01</Day>
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<Title>Life sciences</Title>
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<ArticleTitle>7-O-geranylquercetin-induced autophagy contributes to apoptosis via ROS generation in human non-small cell lung cancer cells.</ArticleTitle>
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<AbstractText Label="AIMS" NlmCategory="OBJECTIVE">To investigate the antitumor effects of 7-O-geranylquercetin (GQ), a novel O-alkylated derivative of quercetin, against non-small cell lung cancer (NSCLC) cell lines A549 and NCI-H1975 and the corresponding mechanisms.</AbstractText>
<AbstractText Label="MAIN METHODS" NlmCategory="METHODS">Cell viability was assessed using MTT assay. The expression of proteins involved in apoptosis and autophagy was measured using western blotting. Besides, apoptosis was determined with DAPI staining, Annexin V-PI staining and transmission electron microscopy (TEM) assay, and autophagy was observed with TEM assay. Cell cycle and reactive oxygen species (ROS) level were detected using flow cytometry.</AbstractText>
<AbstractText Label="KEY FINDINGS" NlmCategory="RESULTS">GQ inhibited viability of A549 and NCI-H1975 cells in a dose- and time-dependent manner without apparent cytotoxicity to normal human lung fibroblast cells. GQ down-regulated the expression of apoptosis-related proteins pro-caspase 3 and Bcl-2, and up-regulated the expression of cleaved-PARP and Bax in A549 and NCI-H1975 cells. Meanwhile, GQ-induced cell apoptosis could be attenuated by caspase inhibitor Z-VAD-FMK. Besides, GQ induced autophagosome formation in A549 and NCI-H1975 cells, promoted the expression of autophagy-related proteins LC3-II and Beclin 1, and suppressed the expression of p62. Autophagy inhibition with chloroquine or Beclin 1 siRNA could effectively inhibit GQ-induced apoptosis. Furthermore, GQ treatment increased the generation of ROS, and ROS inhibitor N-acetylcysteine could reverse GQ-induced autophagy and apoptosis. Taken together, GQ could induce apoptosis and autophagy via ROS generation in A549 and NCI-H1975 cells, and GQ-induced autophagy contributed to apoptosis.</AbstractText>
<AbstractText Label="SIGNIFICANCE" NlmCategory="CONCLUSIONS">Our findings highlight that GQ is a promising anticancer agent for the treatment of lung cancer.</AbstractText>
<CopyrightInformation>Copyright © 2017 Elsevier Inc. All rights reserved.</CopyrightInformation>
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   |type=    RBID
   |clé=     pubmed:28495516
   |texte=   7-O-geranylquercetin-induced autophagy contributes to apoptosis via ROS generation in human non-small cell lung cancer cells.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Corpus/RBID.i   -Sk "pubmed:28495516" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a ChloroquineV1 

Wicri

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