{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Janacova L"],"funding":["Ministerstvo Zdravotnictví Ceské Republiky","Ministerstvo Školství, Mládeže a Tělovýchovy"],"pagination":["1285"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9870911"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["Catechol-O-methyl transferase (COMT) is involved in detoxification of catechol estrogens, playing cancer-protective role in cells producing or utilizing estrogen. Moreover, COMT suppressed migration potential of breast cancer (BC) cells. To delineate COMT role in metastasis of estrogen receptor (ER) dependent BC, we investigated the effect of COMT overexpression on invasion, transcriptome, proteome and interactome of MCF7 cells, a luminal A BC model, stably transduced with lentiviral vector carrying COMT gene (MCF7-COMT). 2D and 3D assays revealed that COMT overexpression associates with decreased cell invasion (p < 0.0001 for Transwell assay, p < 0.05 for spheroid formation). RNA-Seq and LC-DIA-MS/MS proteomics identified genes associated with invasion (FTO, PIR, TACSTD2, ANXA3, KRT80, S1"],"journal":["Scientific reports"],"pubmed_title":["Catechol-O-methyl transferase suppresses cell invasion and interplays with MET signaling in estrogen dependent breast cancer."],"pmcid":["PMC9870911"],"funding_grant_id":["LX22NPO5102","LM2018127","LM2018129","NU22-08-00230"],"pubmed_authors":["Bouchalova P","Lapcik P","Janacova L","Stenckova M","Muller P","Hrachovinova S","Potesil D","Hrstka R","Bouchal P"],"additional_accession":[]},"is_claimable":false,"name":"Catechol-O-methyl transferase suppresses cell invasion and interplays with MET signaling in estrogen dependent breast cancer.","description":"Catechol-O-methyl transferase (COMT) is involved in detoxification of catechol estrogens, playing cancer-protective role in cells producing or utilizing estrogen. Moreover, COMT suppressed migration potential of breast cancer (BC) cells. To delineate COMT role in metastasis of estrogen receptor (ER) dependent BC, we investigated the effect of COMT overexpression on invasion, transcriptome, proteome and interactome of MCF7 cells, a luminal A BC model, stably transduced with lentiviral vector carrying COMT gene (MCF7-COMT). 2D and 3D assays revealed that COMT overexpression associates with decreased cell invasion (p < 0.0001 for Transwell assay, p < 0.05 for spheroid formation). RNA-Seq and LC-DIA-MS/MS proteomics identified genes associated with invasion (FTO, PIR, TACSTD2, ANXA3, KRT80, S1","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Jan","modification":"2025-04-21T22:08:17.209Z","creation":"2025-04-05T18:36:58.26Z"},"accession":"S-EPMC9870911","cross_references":{"pubmed":["36690660"],"doi":["10.1038/s41598-023-28078-1"]}}