Serveur d'exploration Chloroquine

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Synergistic anti-tumour effects of tetrandrine and chloroquine combination therapy in human cancer: a potential antagonistic role for p21.

Identifieur interne : 000E72 ( Main/Exploration ); précédent : 000E71; suivant : 000E73

Synergistic anti-tumour effects of tetrandrine and chloroquine combination therapy in human cancer: a potential antagonistic role for p21.

Auteurs : Liufeng Mei [République populaire de Chine] ; Yicheng Chen ; Zhimeng Wang ; Jian Wang ; Jiali Wan ; Chunrong Yu ; Xin Liu ; Wenhua Li

Source :

RBID : pubmed:25521075

Descripteurs français

English descriptors

Abstract

Tetrandrine, a bisbenzylisoquinoline alkaloid isolated from the Chinese medicinal herb Stephaniae tetrandrae, has a long history in Chinese clinical applications to treat diverse diseases. Tetrandrine induced apoptosis or, at low concentrations, autophagy of human hepatocellular carcinoma cells. Here we have tested the effects of inhibitors of autophagy such as chloroquine, on the response to low concentrations of tetrandrine in cancer cells.

DOI: 10.1111/bph.13045
PubMed: 25521075


Affiliations:


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Le document en format XML

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<term>Apoptosis (drug effects)</term>
<term>Autophagy (drug effects)</term>
<term>Benzylisoquinolines (pharmacology)</term>
<term>Caspase 3 (metabolism)</term>
<term>Cell Survival (drug effects)</term>
<term>Chloroquine (pharmacology)</term>
<term>Colonic Neoplasms (drug therapy)</term>
<term>Colonic Neoplasms (genetics)</term>
<term>Colonic Neoplasms (metabolism)</term>
<term>Colonic Neoplasms (pathology)</term>
<term>Cyclin-Dependent Kinase Inhibitor p21 (genetics)</term>
<term>Cyclin-Dependent Kinase Inhibitor p21 (metabolism)</term>
<term>Dose-Response Relationship, Drug</term>
<term>Drug Synergism</term>
<term>HCT116 Cells</term>
<term>HeLa Cells</term>
<term>Humans</term>
<term>Lung Neoplasms (drug therapy)</term>
<term>Lung Neoplasms (genetics)</term>
<term>Lung Neoplasms (metabolism)</term>
<term>Lung Neoplasms (pathology)</term>
<term>Male</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Nude</term>
<term>Oxidative Stress (drug effects)</term>
<term>Reactive Oxygen Species (metabolism)</term>
<term>Signal Transduction (drug effects)</term>
<term>Time Factors</term>
<term>Transfection</term>
<term>Tumor Burden (drug effects)</term>
<term>Xenograft Model Antitumor Assays</term>
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<term>Animaux</term>
<term>Apoptose ()</term>
<term>Autophagie ()</term>
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<term>Caspase-3 (métabolisme)</term>
<term>Cellules HCT116</term>
<term>Cellules HeLa</term>
<term>Charge tumorale ()</term>
<term>Chloroquine (pharmacologie)</term>
<term>Espèces réactives de l'oxygène (métabolisme)</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>Inhibiteur p21 de kinase cycline-dépendante (génétique)</term>
<term>Inhibiteur p21 de kinase cycline-dépendante (métabolisme)</term>
<term>Mâle</term>
<term>Protocoles de polychimiothérapie antinéoplasique (pharmacologie)</term>
<term>Relation dose-effet des médicaments</term>
<term>Souris de lignée BALB C</term>
<term>Souris nude</term>
<term>Stress oxydatif ()</term>
<term>Survie cellulaire ()</term>
<term>Synergie des médicaments</term>
<term>Tests d'activité antitumorale sur modèle de xénogreffe</term>
<term>Transduction du signal ()</term>
<term>Transfection</term>
<term>Tumeurs du côlon (anatomopathologie)</term>
<term>Tumeurs du côlon (génétique)</term>
<term>Tumeurs du côlon (métabolisme)</term>
<term>Tumeurs du côlon (traitement médicamenteux)</term>
<term>Tumeurs du poumon (anatomopathologie)</term>
<term>Tumeurs du poumon (génétique)</term>
<term>Tumeurs du poumon (métabolisme)</term>
<term>Tumeurs du poumon (traitement médicamenteux)</term>
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<term>Cyclin-Dependent Kinase Inhibitor p21</term>
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<term>Cyclin-Dependent Kinase Inhibitor p21</term>
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<term>Chloroquine</term>
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<term>Apoptosis</term>
<term>Autophagy</term>
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<term>Signal Transduction</term>
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<term>Lung Neoplasms</term>
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<term>Colonic Neoplasms</term>
<term>Lung Neoplasms</term>
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<term>Inhibiteur p21 de kinase cycline-dépendante</term>
<term>Tumeurs du côlon</term>
<term>Tumeurs du poumon</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Colonic Neoplasms</term>
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<term>Caspase-3</term>
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<term>Tumeurs du côlon</term>
<term>Tumeurs du poumon</term>
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<term>Dose-Response Relationship, Drug</term>
<term>Drug Synergism</term>
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<term>HeLa Cells</term>
<term>Humans</term>
<term>Male</term>
<term>Mice, Inbred BALB C</term>
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<term>Charge tumorale</term>
<term>Facteurs temps</term>
<term>Humains</term>
<term>Mâle</term>
<term>Relation dose-effet des médicaments</term>
<term>Souris de lignée BALB C</term>
<term>Souris nude</term>
<term>Stress oxydatif</term>
<term>Survie cellulaire</term>
<term>Synergie des médicaments</term>
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<front>
<div type="abstract" xml:lang="en">Tetrandrine, a bisbenzylisoquinoline alkaloid isolated from the Chinese medicinal herb Stephaniae tetrandrae, has a long history in Chinese clinical applications to treat diverse diseases. Tetrandrine induced apoptosis or, at low concentrations, autophagy of human hepatocellular carcinoma cells. Here we have tested the effects of inhibitors of autophagy such as chloroquine, on the response to low concentrations of tetrandrine in cancer cells.</div>
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<name sortKey="Li, Wenhua" sort="Li, Wenhua" uniqKey="Li W" first="Wenhua" last="Li">Wenhua Li</name>
<name sortKey="Liu, Xin" sort="Liu, Xin" uniqKey="Liu X" first="Xin" last="Liu">Xin Liu</name>
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<name sortKey="Wang, Jian" sort="Wang, Jian" uniqKey="Wang J" first="Jian" last="Wang">Jian Wang</name>
<name sortKey="Wang, Zhimeng" sort="Wang, Zhimeng" uniqKey="Wang Z" first="Zhimeng" last="Wang">Zhimeng Wang</name>
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