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dc.contributor.authorARECHAGA OCAMPO, ELENA-
dc.contributor.authorGONZALEZ DE LA ROSA, CLAUDIA HAYDEE-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/40111">ELENA ARECHAGA OCAMPO</dc:creator>-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/40114">CLAUDIA HAYDEE GONZALEZ DE LA ROSA</dc:creator>-
dc.coverage.temporal<dc:subject>info:eu-repo/classification/cti/2</dc:subject>-
dc.date.issued2013-
dc.identifier.urihttp://ilitia.cua.uam.mx:8080/jspui/handle/123456789/50-
dc.description.abstractAll-trans retinoic acid (ATRA) is currently being used in clinical trials for cancer treatment. The use of ATRA is limited because some cancers, such as lung cancer, show resistance to treatment. However, little is known about the molecular mechanisms that regulate resistance to ATRA treatment. Akt is a kinase that plays a key role in cell survival and cell invasion. Akt is often activated in lung cancer, suggesting its participation in resistance to chemotherapy. In this study, we explored the hypothesis that activation of the Akt pathway promotes resistance to ATRA treatment at the inhibition of cell survival and invasion in lung cancer. We aimed to provide guidelines for the proper use of ATRA in clinical trials and to elucidate basic biological mechanisms of resistance.en_US
dc.language.isoEspañolen_US
dc.publisherMolecular Cancer 2013, 12:44en_US
dc.rightshttp://www.molecular-cancer.com/content/12/1/44-
dc.rightshttps://doi.org/10.1186/1476-4598-12-44-
dc.subjectCáncer de Pulmón,en_US
dc.subjectATRAen_US
dc.subjectResistencia, vía PI3k / Akt, RAR, RAC,en_US
dc.subjectInvasión Celularen_US
dc.titleActivation of Akt pathway by transcription-independent mechanisms of retinoic acid promotes survival and invasion in lung cancer cellsen_US
dc.typeArtículoen_US
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