<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Waller V</submitter><funding>Swiss National Science Foundation</funding><funding>Vontobel-Stiftung</funding><funding>Swiss Cancer Research Foundation</funding><pagination>676583</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8155607</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11</volume><pubmed_abstract>Besides cytotoxic DNA damage irradiation of tumor cells triggers multiple intra- and intercellular signaling processes, that are part of a multilayered, treatment-induced stress response at the unicellular and tumor pathophysiological level. These processes are intertwined with intrinsic and acquired resistance mechanisms to the toxic effects of ionizing radiation and thereby co-determine the tumor response to radiotherapy. Proteolysis of structural elements and bioactive signaling moieties represents a major class of posttranslational modifications regulating intra- and intercellular communication. Plasma membrane-located and secreted metalloproteinases comprise a family of metal-, usually zinc-, dependent endopeptidases and sheddases with a broad variety of substrates including component</pubmed_abstract><journal>Frontiers in oncology</journal><pubmed_title>Combined Radiochemotherapy: Metalloproteinases Revisited.</pubmed_title><pmcid>PMC8155607</pmcid><funding_grant_id>172885</funding_grant_id><pubmed_authors>Waller V</pubmed_authors><pubmed_authors>Pruschy M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combined Radiochemotherapy: Metalloproteinases Revisited.</name><description>Besides cytotoxic DNA damage irradiation of tumor cells triggers multiple intra- and intercellular signaling processes, that are part of a multilayered, treatment-induced stress response at the unicellular and tumor pathophysiological level. These processes are intertwined with intrinsic and acquired resistance mechanisms to the toxic effects of ionizing radiation and thereby co-determine the tumor response to radiotherapy. Proteolysis of structural elements and bioactive signaling moieties represents a major class of posttranslational modifications regulating intra- and intercellular communication. Plasma membrane-located and secreted metalloproteinases comprise a family of metal-, usually zinc-, dependent endopeptidases and sheddases with a broad variety of substrates including component</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-05T00:16:12.523Z</modification><creation>2022-02-10T13:20:30.355Z</creation></dates><accession>S-EPMC8155607</accession><cross_references><pubmed>34055644</pubmed><doi>10.3389/fonc.2021.676583</doi></cross_references></HashMap>