<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Guo W</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Peptidylarginine deiminase (PAD) catalyzes the conversion of arginine residues to citrulline residues, termed citrullination. Recent studies have suggested that PAD isoform 2 (PADI2) plays an important role in tumors, although its tumorigenic effect and mechanism are largely unknown.&lt;h4>Materials and methods&lt;/h4>Immunohistochemistry and enzyme-linked immunosorbent assay (ELISA) were used to investigate the expression level of PADI2 in various tumor tissues and patient blood samples, respectively. MNK-45 and Bel-7402 tumor cell lines originating from gastric and liver tumors, respectively, were treated with anti-PADI2 siRNA, and the subsequent cell proliferation, apoptosis and migration were observed. Polymerase chain reaction (PCR) arrays, including Cancer PathwayFinder,</pubmed_abstract><journal>OncoTargets and therapy</journal><pagination>1475-1485</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5352236</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Investigating the expression, effect and tumorigenic pathway of PADI2 in tumors.</pubmed_title><pmcid>PMC5352236</pmcid><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Xu B</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Ma F</pubmed_authors><pubmed_authors>Chang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Investigating the expression, effect and tumorigenic pathway of PADI2 in tumors.</name><description>&lt;h4>Background&lt;/h4>Peptidylarginine deiminase (PAD) catalyzes the conversion of arginine residues to citrulline residues, termed citrullination. Recent studies have suggested that PAD isoform 2 (PADI2) plays an important role in tumors, although its tumorigenic effect and mechanism are largely unknown.&lt;h4>Materials and methods&lt;/h4>Immunohistochemistry and enzyme-linked immunosorbent assay (ELISA) were used to investigate the expression level of PADI2 in various tumor tissues and patient blood samples, respectively. MNK-45 and Bel-7402 tumor cell lines originating from gastric and liver tumors, respectively, were treated with anti-PADI2 siRNA, and the subsequent cell proliferation, apoptosis and migration were observed. Polymerase chain reaction (PCR) arrays, including Cancer PathwayFinder,</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-26T17:32:21.891Z</modification><creation>2019-03-27T02:38:43Z</creation></dates><accession>S-EPMC5352236</accession><cross_references><pubmed>28331341</pubmed><doi>10.2147/OTT.S92389</doi></cross_references></HashMap>