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MicroRNA-106a targets autophagy and enhances sensitivity of lung cancer cells to Src inhibitors.

Identifieur interne : 000D07 ( Main/Exploration ); précédent : 000D06; suivant : 000D08

MicroRNA-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 :

RBID : pubmed:27372519

Descripteurs français

English descriptors

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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<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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<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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<term>Autophagy-Related Protein-1 Homolog</term>
<term>Intracellular Signaling Peptides and Proteins</term>
<term>MicroRNAs</term>
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<term>Carcinome pulmonaire non à petites cellules</term>
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<term>Tumeurs du poumon</term>
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<term>Cell Movement</term>
<term>Cell Survival</term>
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<term>Adenocarcinoma</term>
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<term>Carcinome pulmonaire non à petites cellules</term>
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<term>src-Family kinases</term>
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<term>Adenocarcinoma</term>
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<term>Lung Neoplasms</term>
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<term>Dasatinib</term>
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<term>Carcinome pulmonaire non à petites cellules</term>
<term>Tumeurs du poumon</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Adenocarcinoma of Lung</term>
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<term>Microtubule-Associated Proteins</term>
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<term>Humains</term>
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<term>Petit ARN interférent</term>
<term>Protéines associées aux microtubules</term>
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<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>
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