<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Graham RLJ</submitter><funding>Medical Research Council</funding><funding>Mastocytosis Charity</funding><pagination>5087</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8948255</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(1)</volume><pubmed_abstract>Mastocytosis is a rare myeloproliferative disease, characterised by accumulation of neoplastic mast cells in one or several organs. It presents as cutaneous or systemic. Patients with advanced systemic mastocytosis have a median survival of 3.5 years. The aetiology of mastocytosis is poorly understood, patients present with a broad spectrum of varying clinical symptoms that lack specificity to point clearly to a definitive diagnosis. Discovery of novel blood borne biomarkers would provide a tractable method for rapid identification of mastocytosis and its sub-types. Moving towards this goal, we carried out a clinical biomarker study on blood from twenty individuals (systemic mastocytosis: n = 12, controls: n = 8), which were subjected to global proteome investigation using the novel techno</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>SWATH-MS identification of CXCL7, LBP, TGFβ1 and PDGFRβ as novel biomarkers in human systemic mastocytosis.</pubmed_title><pmcid>PMC8948255</pmcid><funding_grant_id>MR/P016502/1</funding_grant_id><pubmed_authors>Myers B</pubmed_authors><pubmed_authors>McMullen AA</pubmed_authors><pubmed_authors>Graham C</pubmed_authors><pubmed_authors>Graham RLJ</pubmed_authors><pubmed_authors>Dempsey-Hibbert NC</pubmed_authors><pubmed_authors>Moore G</pubmed_authors></additional><is_claimable>false</is_claimable><name>SWATH-MS identification of CXCL7, LBP, TGFβ1 and PDGFRβ as novel biomarkers in human systemic mastocytosis.</name><description>Mastocytosis is a rare myeloproliferative disease, characterised by accumulation of neoplastic mast cells in one or several organs. It presents as cutaneous or systemic. Patients with advanced systemic mastocytosis have a median survival of 3.5 years. The aetiology of mastocytosis is poorly understood, patients present with a broad spectrum of varying clinical symptoms that lack specificity to point clearly to a definitive diagnosis. Discovery of novel blood borne biomarkers would provide a tractable method for rapid identification of mastocytosis and its sub-types. Moving towards this goal, we carried out a clinical biomarker study on blood from twenty individuals (systemic mastocytosis: n = 12, controls: n = 8), which were subjected to global proteome investigation using the novel techno</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-05-18T12:06:53.913Z</modification><creation>2025-05-18T12:06:53.913Z</creation></dates><accession>S-EPMC8948255</accession><cross_references><pubmed>35332176</pubmed><doi>10.1038/s41598-022-08345-3</doi></cross_references></HashMap>