Inhibition of focal adhesion kinase with her-2 targeted antibody pertuzumab (Omnitarg®, 2C4) in breast cancer cells
dc.authorid | Canbay, Emel/0000-0001-7592-3000 | |
dc.authorid | Dedeoglu, Bala Gur/0000-0002-4320-5685 | |
dc.authorid | Yulug, Isik/0000-0002-7577-2502 | |
dc.authorwosid | Canbay, Emel/AAA-8582-2022 | |
dc.authorwosid | Dedeoglu, Bala Gur/ABC-2436-2020 | |
dc.contributor.author | Canbay, Emel | |
dc.contributor.author | Gur-Dedeoglu, Bala | |
dc.contributor.author | Bozkurt, Betul | |
dc.contributor.author | Karabeyoglu, Melih | |
dc.contributor.author | Unal, Bulent | |
dc.contributor.author | Yildirim, Osman | |
dc.contributor.author | Cengiz, Omer | |
dc.date.accessioned | 2024-08-04T20:32:18Z | |
dc.date.available | 2024-08-04T20:32:18Z | |
dc.date.issued | 2008 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Pertuzumab (Omnitarg (R), 2C4) is a recombinant humanized monoclonal antibody targeted to extracellular region of HER-2. Previous results proved the inhibitory effect of Pertuzumab on the survival of breast cancer cells via MAPK and AM pathway. Focal adhesion kinase (FAK) regulates multiple cellular processes including growth, differentiation, adhesion, motility and apoptosis. Here, we aimed to investigate the effects of Pertuzumab on ligand activated total FAK expression and phosphorylation in the HER-2 overexpressing BT-474 breast cancer cell line. Heregulin,vas used for ligand activation. We have found that FAK expression and phosphorylation were inhibited in with Pertuzumab in breast cancer cells. | en_US |
dc.description.sponsorship | T.R.State Planing Organization [T-256] | en_US |
dc.description.sponsorship | We thank Ms Dina Washington for Pertuzumab (Omnitarg (R), Genentech). This work Was supported by T.R.State Planing Organization Project No: T-256 (E.C.). EC is rotational specialist in Department of General Surgery, Breast Unit, Istanbul University, Istanbul Medical Faculty. | en_US |
dc.identifier.endpage | 299 | en_US |
dc.identifier.issn | 1529-9120 | |
dc.identifier.scopus | 2-s2.0-77649139830 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 293 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/94988 | |
dc.identifier.volume | 12B | en_US |
dc.identifier.wos | WOS:000265623400015 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Gene Therapy Press | en_US |
dc.relation.ispartof | Gene Therapy and Molecular Biology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Pertuzumab | en_US |
dc.subject | Omnitarg (R) | en_US |
dc.subject | 2C4 | en_US |
dc.subject | focal adhesion kinase | en_US |
dc.subject | breast cancer | en_US |
dc.title | Inhibition of focal adhesion kinase with her-2 targeted antibody pertuzumab (Omnitarg®, 2C4) in breast cancer cells | en_US |
dc.type | Article | en_US |