<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2019</volume><submitter>Borchert S</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Malignant pleural mesothelioma (MPM) is a rare, predominantly asbestos-related and biologically highly aggressive tumor associated with a dismal prognosis. Multimodal therapy consisting of platinum-based chemotherapy is the treatment of choice. The reasons underlying the rather poor efficacy of platinum compounds remain largely unknown. Kinase activity might influence cellular response to these regimens.&lt;h4>Materials and methods&lt;/h4>For this exploratory study, we screened MPM cell lines (NCI-H2452, NCI-H2052, and MSTO-211H) differing in response to cisplatin and benign control fibroblasts (MRC-5) for overall phosphorylation patterns as well as kinase activity with respect to cellular response to cisplatin-based therapeutics. We analysed the cell lines for cellular kinase</pubmed_abstract><journal>Journal of oncology</journal><pagination>2902985</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6942867</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Screening of Pleural Mesothelioma Cell Lines for Kinase Activity May Identify New Mechanisms of Therapy Resistance in Patients Receiving Platin-Based Chemotherapy.</pubmed_title><pmcid>PMC6942867</pmcid><pubmed_authors>Hegedus B</pubmed_authors><pubmed_authors>Mairinger E</pubmed_authors><pubmed_authors>Aigner C</pubmed_authors><pubmed_authors>Herold T</pubmed_authors><pubmed_authors>Eberhardt WEE</pubmed_authors><pubmed_authors>Wohlschlaeger J</pubmed_authors><pubmed_authors>Hager T</pubmed_authors><pubmed_authors>Wessolly M</pubmed_authors><pubmed_authors>Mairinger FD</pubmed_authors><pubmed_authors>Bankfalvi A</pubmed_authors><pubmed_authors>Borchert S</pubmed_authors><pubmed_authors>Walter RFH</pubmed_authors><pubmed_authors>Suckrau PM</pubmed_authors><pubmed_authors>Schmid KW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Screening of Pleural Mesothelioma Cell Lines for Kinase Activity May Identify New Mechanisms of Therapy Resistance in Patients Receiving Platin-Based Chemotherapy.</name><description>&lt;h4>Background&lt;/h4>Malignant pleural mesothelioma (MPM) is a rare, predominantly asbestos-related and biologically highly aggressive tumor associated with a dismal prognosis. Multimodal therapy consisting of platinum-based chemotherapy is the treatment of choice. The reasons underlying the rather poor efficacy of platinum compounds remain largely unknown. Kinase activity might influence cellular response to these regimens.&lt;h4>Materials and methods&lt;/h4>For this exploratory study, we screened MPM cell lines (NCI-H2452, NCI-H2052, and MSTO-211H) differing in response to cisplatin and benign control fibroblasts (MRC-5) for overall phosphorylation patterns as well as kinase activity with respect to cellular response to cisplatin-based therapeutics. We analysed the cell lines for cellular kinase</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-04-15T13:20:51.138Z</modification><creation>2025-05-29T22:04:55.266Z</creation></dates><accession>S-EPMC6942867</accession><cross_references><pubmed>31929796</pubmed><doi>10.1155/2019/2902985</doi></cross_references></HashMap>