<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(11)</volume><submitter>Shahid S</submitter><pubmed_abstract>Peritoneal metastasis (PM) is a very serious complication of gastrointestinal and gynecological malignancies which is poorly documented. Modified mesothelial cell layer and their microenvironments can favor fibrin deposition for cancer cell adhesion. Scanning and transmission electron microscopy of peritoneal surface and cancer cell clusters from cancer patients was done. Ascites and its impact on mesothelial cells were assessed by cytokine array. Neprilysin, matrix metalloprotease, epithelial mesenchymal transition (EMT) related molecules (E-cadherin, Snail, Slug, Twist, Vimentin and Fibronectin), tissues factor (TF), endothelial protein C receptors (EPCR) were quantified by q-PCR. Fibrin in the simples were stained using anti fibrin F1E1 antibody. Migration ability was assessed by scratc</pubmed_abstract><journal>Neoplasia (New York, N.Y.)</journal><pagination>1091-1101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6889015</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Fibrin Deposit on the Peritoneal Surface Serves as a Niche for Cancer Expansion in Carcinomatosis Patients.</pubmed_title><pmcid>PMC6889015</pmcid><pubmed_authors>Shahid S</pubmed_authors><pubmed_authors>Assaf A</pubmed_authors><pubmed_authors>Massoud M</pubmed_authors><pubmed_authors>Matti U</pubmed_authors><pubmed_authors>Eveno C</pubmed_authors><pubmed_authors>Marc P</pubmed_authors><pubmed_authors>Iman A</pubmed_authors><pubmed_authors>Rachid K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fibrin Deposit on the Peritoneal Surface Serves as a Niche for Cancer Expansion in Carcinomatosis Patients.</name><description>Peritoneal metastasis (PM) is a very serious complication of gastrointestinal and gynecological malignancies which is poorly documented. Modified mesothelial cell layer and their microenvironments can favor fibrin deposition for cancer cell adhesion. Scanning and transmission electron microscopy of peritoneal surface and cancer cell clusters from cancer patients was done. Ascites and its impact on mesothelial cells were assessed by cytokine array. Neprilysin, matrix metalloprotease, epithelial mesenchymal transition (EMT) related molecules (E-cadherin, Snail, Slug, Twist, Vimentin and Fibronectin), tissues factor (TF), endothelial protein C receptors (EPCR) were quantified by q-PCR. Fibrin in the simples were stained using anti fibrin F1E1 antibody. Migration ability was assessed by scratc</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2025-04-04T20:45:35.035Z</modification><creation>2020-05-21T21:41:05Z</creation></dates><accession>S-EPMC6889015</accession><cross_references><pubmed>31734630</pubmed><doi>10.1016/j.neo.2019.08.006</doi></cross_references></HashMap>