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dc.contributor.authorBhuvaneswari, Ramaswamy
dc.contributor.authorGan, Yik
dc.contributor.authorSoo, Khee
dc.contributor.authorOlivo, Malini
dc.date.accessioned2018-09-20T16:01:01Z
dc.date.available2018-09-20T16:01:01Z
dc.date.issued2009-01-01
dc.identifier.citationBhuvaneswari, Ramaswamy; Gan, Yik; Soo, Khee; Olivo, Malini (2009). Targeting egfr with photodynamic therapy in combination with erbitux enhances in vivo bladder tumor response. Molecular Cancer 8 ,
dc.identifier.issn1476-4598
dc.identifier.urihttp://hdl.handle.net/10379/10429
dc.description.abstractBackground: Photodynamic therapy (PDT) is a promising cancer treatment modality that involves the interaction of the photosensitizer, molecular oxygen and light of specific wavelength to destroy tumor cells. Treatment induced hypoxia is one of the main side effects of PDT and efforts are underway to optimize PDT protocols for improved efficacy. The aim of this study was to investigate the anti-tumor effects of PDT plus Erbitux, an angiogenesis inhibitor that targets epidermal growth factor receptor (EGFR), on human bladder cancer model. Tumor-bearing nude mice were assigned to four groups that included control, PDT, Erbitux and PDT plus Erbitux and tumor volume was charted over 90-day period. Results: Our results demonstrate that combination of Erbitux with PDT strongly inhibits tumor growth in the bladder tumor xenograft model when compared to the other groups. Downregulation of EGFR was detected using immunohistochemistry, immunofluorescence and western blotting. Increased apoptosis was associated with tumor inhibition in the combination therapy group. In addition, we identified the dephosphorylation of ErbB4 at tyrosine 1284 site to play a major role in tumor inhibition. Also, at the RNA level downregulation of EGFR target genes cyclin D1 and c-myc was observed in tumors treated with PDT plus Erbitux. Conclusion: The combination therapy of PDT and Erbitux effectively inhibits tumor growth and is a promising therapeutic approach in the treatment of bladder tumors.
dc.publisherSpringer Nature
dc.relation.ispartofMolecular Cancer
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Ireland
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/ie/
dc.subjectgrowth-factor receptor
dc.subjectsquamous-cell carcinoma
dc.subjectmetastatic colorectal-cancer
dc.subject5-aminolevulinic acid
dc.subjectmonoclonal-antibody
dc.subjectcetuximab
dc.subjecthead
dc.subjectneck
dc.subjectblockade
dc.subjectphosphorylation
dc.titleTargeting egfr with photodynamic therapy in combination with erbitux enhances in vivo bladder tumor response
dc.typeArticle
dc.identifier.doi10.1186/1476-4598-8-94
dc.local.publishedsourcehttps://molecular-cancer.biomedcentral.com/track/pdf/10.1186/1476-4598-8-94?site=molecular-cancer.biomedcentral.com
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Attribution-NonCommercial-NoDerivs 3.0 Ireland
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Ireland