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Cells ; 9(4)2020 04 20.
Article in English | MEDLINE | ID: mdl-32326079

ABSTRACT

Malignant pleural mesothelioma (MPM) has extremely limited treatment despite a poor prognosis. Moreover, molecular targeted therapy for MPM has not yet been implemented; thus, a new targeted therapy is highly desirable. Near-infrared photoimmunotherapy (NIR-PIT) is a recently developed cancer therapy that combines the specificity of antibodies for targeting tumors with toxicity induced by the photoabsorber after exposure to NIR-light. In this study, we developed a new phototherapy targeting podoplanin (PDPN) for MPM with the use of both NIR-PIT and an anti-PDPN antibody, NZ-1. An antibody-photosensitizer conjugate consisting of NZ-1 and phthalocyanine dye was synthesized. In vitro NIR-PIT-induced cytotoxicity was measured with both dead cell staining and luciferase activity on various MPM cell lines. In vivo NIR-PIT was examined in both the flank tumor and orthotopic mouse model with in vivo real-time imaging. In vitro NIR-PIT-induced cytotoxicity was NIR-light dose dependent. In vivo NIR-PIT led to significant reduction in both tumor volume and luciferase activity in a flank model (p < 0.05, NIR-PIT group versus NZ-1-IR700 group). The PDPN-targeted NIR-PIT resulted in a significant antitumor effect in an MPM orthotopic mouse model (p < 0.05, NIR-PIT group versus NZ-1-IR700 group). This study suggests that PDPN-targeted NIR-PIT could be a new promising treatment for MPM.


Subject(s)
Immunoconjugates/pharmacology , Lung Neoplasms/immunology , Mesothelioma, Malignant/drug therapy , Mesothelioma, Malignant/immunology , Molecular Targeted Therapy , Animals , Cell Line, Tumor , Humans , Immunotherapy/methods , Lung Neoplasms/drug therapy , Membrane Glycoproteins/drug effects , Mesothelioma, Malignant/pathology , Mice, Nude , Phototherapy/methods , Xenograft Model Antitumor Assays/methods
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