MicroRNA-106a targets autophagy and enhances sensitivity of lung cancer cells to Src inhibitors.
Identifieur interne : 000D07 ( Main/Exploration ); précédent : 000D06; suivant : 000D08MicroRNA-106a targets autophagy and enhances sensitivity of lung cancer cells to Src inhibitors.
Auteurs : Sacha I. Rothschild [Suisse] ; Oliver Gautschi [Suisse] ; Jasmin Batliner [Suisse] ; Mathias Gugger [Suisse] ; Martin F. Fey [Suisse] ; Mario P. Tschan [Suisse]Source :
- Lung cancer (Amsterdam, Netherlands) [ 1872-8332 ] ; 2017.
Descripteurs français
- KwdFr :
- Adénocarcinome (anatomopathologie), Adénocarcinome (génétique), Adénocarcinome (traitement médicamenteux), Autophagie (), Benzodioxoles (pharmacologie), Carcinome pulmonaire non à petites cellules (anatomopathologie), Carcinome pulmonaire non à petites cellules (génétique), Carcinome pulmonaire non à petites cellules (traitement médicamenteux), Dasatinib (pharmacologie), Homologue de la protéine-1 associée à l'autophagie (génétique), Humains, Inhibiteurs de protéines kinases (pharmacologie), Mouvement cellulaire (), Petit ARN interférent, Poumon (anatomopathologie), Protéines associées aux microtubules, Protéines et peptides de signalisation intracellulaire (génétique), Quinazolines (pharmacologie), Régulation négative (), Survie cellulaire (), Transduction du signal (), Tumeurs du poumon (anatomopathologie), Tumeurs du poumon (génétique), Tumeurs du poumon (traitement médicamenteux), microARN (génétique), src-Family kinases (antagonistes et inhibiteurs), src-Family kinases (métabolisme), src-Family kinases (pharmacologie).
- MESH :
- anatomopathologie : Adénocarcinome, Carcinome pulmonaire non à petites cellules, Poumon, Tumeurs du poumon.
- antagonistes et inhibiteurs : src-Family kinases.
- génétique : Adénocarcinome, Carcinome pulmonaire non à petites cellules, Homologue de la protéine-1 associée à l'autophagie, Protéines et peptides de signalisation intracellulaire, Tumeurs du poumon, microARN.
- métabolisme : src-Family kinases.
- pharmacologie : Benzodioxoles, Dasatinib, Inhibiteurs de protéines kinases, Quinazolines, src-Family kinases.
- traitement médicamenteux : Adénocarcinome, Carcinome pulmonaire non à petites cellules, Tumeurs du poumon.
- Autophagie, Humains, Mouvement cellulaire, Petit ARN interférent, Protéines associées aux microtubules, Régulation négative, Survie cellulaire, Transduction du signal.
English descriptors
- KwdEn :
- Adenocarcinoma (drug therapy), Adenocarcinoma (genetics), Adenocarcinoma (pathology), Adenocarcinoma of Lung, Autophagy (drug effects), Autophagy-Related Protein-1 Homolog (genetics), Benzodioxoles (pharmacology), Carcinoma, Non-Small-Cell Lung (drug therapy), Carcinoma, Non-Small-Cell Lung (genetics), Carcinoma, Non-Small-Cell Lung (pathology), Cell Movement (drug effects), Cell Survival (drug effects), Dasatinib (pharmacology), Down-Regulation (drug effects), Humans, Intracellular Signaling Peptides and Proteins (genetics), Lung (pathology), Lung Neoplasms (drug therapy), Lung Neoplasms (genetics), Lung Neoplasms (pathology), MicroRNAs (genetics), Microtubule-Associated Proteins, Protein Kinase Inhibitors (pharmacology), Quinazolines (pharmacology), RNA, Small Interfering, Signal Transduction (drug effects), src-Family Kinases (antagonists & inhibitors), src-Family Kinases (metabolism), src-Family Kinases (pharmacology).
- MESH :
- chemical , antagonists & inhibitors : src-Family Kinases.
- chemical , genetics : Autophagy-Related Protein-1 Homolog, Intracellular Signaling Peptides and Proteins, MicroRNAs.
- drug effects : Autophagy, Cell Movement, Cell Survival, Down-Regulation, Signal Transduction.
- drug therapy : Adenocarcinoma, Carcinoma, Non-Small-Cell Lung, Lung Neoplasms.
- genetics : Adenocarcinoma, Carcinoma, Non-Small-Cell Lung, Lung Neoplasms.
- chemical , metabolism : src-Family Kinases.
- pathology : Adenocarcinoma, Carcinoma, Non-Small-Cell Lung, Lung, Lung Neoplasms.
- chemical , pharmacology : Benzodioxoles, Dasatinib, Protein Kinase Inhibitors, Quinazolines, src-Family Kinases.
- Adenocarcinoma of Lung, Humans, Microtubule-Associated Proteins, RNA, Small Interfering.
Abstract
Src tyrosine kinase inhibitors (TKIs) significantly inhibit cell migration and invasion in lung cancer cell lines with minor cytotoxic effects. In clinical trials, however, they show modest activity in combination with chemotherapeutic agents. Possible resistance mechanisms include the induction of cytoprotective autophagy upon Src inhibition. Autophagy is a cellular recycling process that allows cell survival in response to a variety of stress stimuli including responses to various treatments.
DOI: 10.1016/j.lungcan.2016.06.004
PubMed: 27372519
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adenocarcinoma (drug therapy)</term>
<term>Adenocarcinoma (genetics)</term>
<term>Adenocarcinoma (pathology)</term>
<term>Adenocarcinoma of Lung</term>
<term>Autophagy (drug effects)</term>
<term>Autophagy-Related Protein-1 Homolog (genetics)</term>
<term>Benzodioxoles (pharmacology)</term>
<term>Carcinoma, Non-Small-Cell Lung (drug therapy)</term>
<term>Carcinoma, Non-Small-Cell Lung (genetics)</term>
<term>Carcinoma, Non-Small-Cell Lung (pathology)</term>
<term>Cell Movement (drug effects)</term>
<term>Cell Survival (drug effects)</term>
<term>Dasatinib (pharmacology)</term>
<term>Down-Regulation (drug effects)</term>
<term>Humans</term>
<term>Intracellular Signaling Peptides and Proteins (genetics)</term>
<term>Lung (pathology)</term>
<term>Lung Neoplasms (drug therapy)</term>
<term>Lung Neoplasms (genetics)</term>
<term>Lung Neoplasms (pathology)</term>
<term>MicroRNAs (genetics)</term>
<term>Microtubule-Associated Proteins</term>
<term>Protein Kinase Inhibitors (pharmacology)</term>
<term>Quinazolines (pharmacology)</term>
<term>RNA, Small Interfering</term>
<term>Signal Transduction (drug effects)</term>
<term>src-Family Kinases (antagonists & inhibitors)</term>
<term>src-Family Kinases (metabolism)</term>
<term>src-Family Kinases (pharmacology)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adénocarcinome (anatomopathologie)</term>
<term>Adénocarcinome (génétique)</term>
<term>Adénocarcinome (traitement médicamenteux)</term>
<term>Autophagie ()</term>
<term>Benzodioxoles (pharmacologie)</term>
<term>Carcinome pulmonaire non à petites cellules (anatomopathologie)</term>
<term>Carcinome pulmonaire non à petites cellules (génétique)</term>
<term>Carcinome pulmonaire non à petites cellules (traitement médicamenteux)</term>
<term>Dasatinib (pharmacologie)</term>
<term>Homologue de la protéine-1 associée à l'autophagie (génétique)</term>
<term>Humains</term>
<term>Inhibiteurs de protéines kinases (pharmacologie)</term>
<term>Mouvement cellulaire ()</term>
<term>Petit ARN interférent</term>
<term>Poumon (anatomopathologie)</term>
<term>Protéines associées aux microtubules</term>
<term>Protéines et peptides de signalisation intracellulaire (génétique)</term>
<term>Quinazolines (pharmacologie)</term>
<term>Régulation négative ()</term>
<term>Survie cellulaire ()</term>
<term>Transduction du signal ()</term>
<term>Tumeurs du poumon (anatomopathologie)</term>
<term>Tumeurs du poumon (génétique)</term>
<term>Tumeurs du poumon (traitement médicamenteux)</term>
<term>microARN (génétique)</term>
<term>src-Family kinases (antagonistes et inhibiteurs)</term>
<term>src-Family kinases (métabolisme)</term>
<term>src-Family kinases (pharmacologie)</term>
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<keywords scheme="MESH" type="chemical" qualifier="antagonists & inhibitors" xml:lang="en"><term>src-Family Kinases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Autophagy-Related Protein-1 Homolog</term>
<term>Intracellular Signaling Peptides and Proteins</term>
<term>MicroRNAs</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Adénocarcinome</term>
<term>Carcinome pulmonaire non à petites cellules</term>
<term>Poumon</term>
<term>Tumeurs du poumon</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Autophagy</term>
<term>Cell Movement</term>
<term>Cell Survival</term>
<term>Down-Regulation</term>
<term>Signal Transduction</term>
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<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en"><term>Adenocarcinoma</term>
<term>Carcinoma, Non-Small-Cell Lung</term>
<term>Lung Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Adenocarcinoma</term>
<term>Carcinoma, Non-Small-Cell Lung</term>
<term>Lung Neoplasms</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Adénocarcinome</term>
<term>Carcinome pulmonaire non à petites cellules</term>
<term>Homologue de la protéine-1 associée à l'autophagie</term>
<term>Protéines et peptides de signalisation intracellulaire</term>
<term>Tumeurs du poumon</term>
<term>microARN</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>src-Family Kinases</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>src-Family kinases</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Adenocarcinoma</term>
<term>Carcinoma, Non-Small-Cell Lung</term>
<term>Lung</term>
<term>Lung Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Benzodioxoles</term>
<term>Dasatinib</term>
<term>Inhibiteurs de protéines kinases</term>
<term>Quinazolines</term>
<term>src-Family kinases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Benzodioxoles</term>
<term>Dasatinib</term>
<term>Protein Kinase Inhibitors</term>
<term>Quinazolines</term>
<term>src-Family Kinases</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr"><term>Adénocarcinome</term>
<term>Carcinome pulmonaire non à petites cellules</term>
<term>Tumeurs du poumon</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adenocarcinoma of Lung</term>
<term>Humans</term>
<term>Microtubule-Associated Proteins</term>
<term>RNA, Small Interfering</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Autophagie</term>
<term>Humains</term>
<term>Mouvement cellulaire</term>
<term>Petit ARN interférent</term>
<term>Protéines associées aux microtubules</term>
<term>Régulation négative</term>
<term>Survie cellulaire</term>
<term>Transduction du signal</term>
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<front><div type="abstract" xml:lang="en">Src tyrosine kinase inhibitors (TKIs) significantly inhibit cell migration and invasion in lung cancer cell lines with minor cytotoxic effects. In clinical trials, however, they show modest activity in combination with chemotherapeutic agents. Possible resistance mechanisms include the induction of cytoprotective autophagy upon Src inhibition. Autophagy is a cellular recycling process that allows cell survival in response to a variety of stress stimuli including responses to various treatments.</div>
</front>
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</country>
<region><li>Canton de Berne</li>
</region>
<settlement><li>Berne</li>
</settlement>
<orgName><li>Université de Berne</li>
</orgName>
</list>
<tree><country name="Suisse"><noRegion><name sortKey="Rothschild, Sacha I" sort="Rothschild, Sacha I" uniqKey="Rothschild S" first="Sacha I" last="Rothschild">Sacha I. Rothschild</name>
</noRegion>
<name sortKey="Batliner, Jasmin" sort="Batliner, Jasmin" uniqKey="Batliner J" first="Jasmin" last="Batliner">Jasmin Batliner</name>
<name sortKey="Fey, Martin F" sort="Fey, Martin F" uniqKey="Fey M" first="Martin F" last="Fey">Martin F. Fey</name>
<name sortKey="Gautschi, Oliver" sort="Gautschi, Oliver" uniqKey="Gautschi O" first="Oliver" last="Gautschi">Oliver Gautschi</name>
<name sortKey="Gugger, Mathias" sort="Gugger, Mathias" uniqKey="Gugger M" first="Mathias" last="Gugger">Mathias Gugger</name>
<name sortKey="Tschan, Mario P" sort="Tschan, Mario P" uniqKey="Tschan M" first="Mario P" last="Tschan">Mario P. Tschan</name>
</country>
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