<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Corrales E</submitter><funding>Deutsches Krebsforschungszentrum (DKFZ)</funding><funding>Bundesministerium für Bildung und Forschung</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Deutschen Konsortium für Translationale Krebsforschung</funding><pagination>187</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9700886</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Current therapeutic management of advanced melanoma patients largely depends on their BRAF mutation status. However, the vast heterogeneity of the tumors hampers the success of therapies targeting the MAPK/ERK pathway alone. Dissecting this heterogeneity will contribute to identifying key players in the oncogenic progression to tailor more effective therapies.&lt;h4>Methods&lt;/h4>We performed a comprehensive molecular and phenotypic characterization of a panel of patient-derived BRAF&lt;sup>V600E&lt;/sup>-positive melanoma cell lines. Transcriptional profiling was used to identify groups of coregulated genes whose expression relates to an increased migratory potential and a higher resistance.&lt;h4>Results&lt;/h4>A decrease in sensitivity to MAPK/ERK pathway inhibition with vemurafenib o</pubmed_abstract><journal>Cell communication and signaling : CCS</journal><pubmed_title>PI3K/AKT signaling allows for MAPK/ERK pathway independency mediating dedifferentiation-driven treatment resistance in melanoma.</pubmed_title><pmcid>PMC9700886</pmcid><funding_grant_id>GRK2344</funding_grant_id><funding_grant_id>FKZ 01ZZ1801B</funding_grant_id><pubmed_authors>Mertes R</pubmed_authors><pubmed_authors>Kowar S</pubmed_authors><pubmed_authors>Corrales E</pubmed_authors><pubmed_authors>Lemke S</pubmed_authors><pubmed_authors>Boerries M</pubmed_authors><pubmed_authors>Munch J</pubmed_authors><pubmed_authors>Levit-Zerdoun E</pubmed_authors><pubmed_authors>Lehmann A</pubmed_authors><pubmed_authors>Metzger P</pubmed_authors></additional><is_claimable>false</is_claimable><name>PI3K/AKT signaling allows for MAPK/ERK pathway independency mediating dedifferentiation-driven treatment resistance in melanoma.</name><description>&lt;h4>Background&lt;/h4>Current therapeutic management of advanced melanoma patients largely depends on their BRAF mutation status. However, the vast heterogeneity of the tumors hampers the success of therapies targeting the MAPK/ERK pathway alone. Dissecting this heterogeneity will contribute to identifying key players in the oncogenic progression to tailor more effective therapies.&lt;h4>Methods&lt;/h4>We performed a comprehensive molecular and phenotypic characterization of a panel of patient-derived BRAF&lt;sup>V600E&lt;/sup>-positive melanoma cell lines. Transcriptional profiling was used to identify groups of coregulated genes whose expression relates to an increased migratory potential and a higher resistance.&lt;h4>Results&lt;/h4>A decrease in sensitivity to MAPK/ERK pathway inhibition with vemurafenib o</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T20:36:30.31Z</modification><creation>2025-02-19T04:36:57.966Z</creation></dates><accession>S-EPMC9700886</accession><cross_references><pubmed>36434616</pubmed><doi>10.1186/s12964-022-00989-y</doi></cross_references></HashMap>