<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pfeiferova L</submitter><funding>Charles University</funding><funding>Ministry of Education, Youth and Sports of the Czech Republic</funding><funding>Ministry of Health of the Czech Republic</funding><funding>Charles University in Prague</funding><pagination>38</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11893657</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>163(1)</volume><pubmed_abstract>Fibroblasts, the most abundant cell type in the human body, play crucial roles in biological processes such as inflammation and cancer progression. They originate from the mesoderm or neural-crest-derived ectomesenchyme. Ectomesenchyme-derived fibroblasts contribute to facial formation and do not express HOX genes during development. The expression and role of the HOX genes in adult fibroblasts is not known. We investigated whether the developmental pattern persists into adulthood and under pathological conditions, such as cancer. We collected adult fibroblasts of ectomesenchymal and mesodermal origins from distinct body parts. The isolated fibroblasts were characterised by immunocytochemistry, and their transcriptome was analysed by whole genome profiling. Significant differences were obs</pubmed_abstract><journal>Histochemistry and cell biology</journal><pubmed_title>The HOX code of human adult fibroblasts reflects their ectomesenchymal or mesodermal origin.</pubmed_title><pmcid>PMC11893657</pmcid><funding_grant_id>NW24-03-00459</funding_grant_id><funding_grant_id>COOPERATIO-Onco</funding_grant_id><funding_grant_id>LX22NPO5102</funding_grant_id><funding_grant_id>NU22-03-00318</funding_grant_id><pubmed_authors>Hradilova M</pubmed_authors><pubmed_authors>Vymolova B</pubmed_authors><pubmed_authors>Sachova J</pubmed_authors><pubmed_authors>Pienta KJ</pubmed_authors><pubmed_authors>Szabo P</pubmed_authors><pubmed_authors>Busek P</pubmed_authors><pubmed_authors>Gal P</pubmed_authors><pubmed_authors>Smetana K</pubmed_authors><pubmed_authors>Pfeiferova L</pubmed_authors><pubmed_authors>Spanko M</pubmed_authors><pubmed_authors>Machon V</pubmed_authors><pubmed_authors>Lacina L</pubmed_authors><pubmed_authors>Kolar M</pubmed_authors><pubmed_authors>Valach J</pubmed_authors><pubmed_authors>Sedo A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The HOX code of human adult fibroblasts reflects their ectomesenchymal or mesodermal origin.</name><description>Fibroblasts, the most abundant cell type in the human body, play crucial roles in biological processes such as inflammation and cancer progression. They originate from the mesoderm or neural-crest-derived ectomesenchyme. Ectomesenchyme-derived fibroblasts contribute to facial formation and do not express HOX genes during development. The expression and role of the HOX genes in adult fibroblasts is not known. We investigated whether the developmental pattern persists into adulthood and under pathological conditions, such as cancer. We collected adult fibroblasts of ectomesenchymal and mesodermal origins from distinct body parts. The isolated fibroblasts were characterised by immunocytochemistry, and their transcriptome was analysed by whole genome profiling. Significant differences were obs</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-06-06T17:39:05.966Z</modification><creation>2025-04-06T03:20:30.185Z</creation></dates><accession>S-EPMC11893657</accession><cross_references><pubmed>40063181</pubmed><doi>10.1007/s00418-025-02362-9</doi></cross_references></HashMap>