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Targeted Phototherapy for Malignant Pleural Mesothelioma: Near-Infrared Photoimmunotherapy Targeting Podoplanin

Authors :
Yuko Nishinaga
Kazuhide Sato
Hirotoshi Yasui
Shunichi Taki
Kazuomi Takahashi
Misae Shimizu
Rena Endo
Chiaki Koike
Noriko Kuramoto
Shota Nakamura
Takayuki Fukui
Hiroshi Yukawa
Yoshinobu Baba
Mika K. Kaneko
Toyofumi F. Chen-Yoshikawa
Hisataka Kobayashi
Yukinari Kato
Yoshinori Hasegawa
Source :
Cells, Vol 9, Iss 4, p 1019 (2020)
Publication Year :
2020
Publisher :
MDPI AG, 2020.

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.

Details

Language :
English
ISSN :
20734409
Volume :
9
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Cells
Publication Type :
Academic Journal
Accession number :
edsdoj.f404b554e2c84019be1ed7f1fb222914
Document Type :
article
Full Text :
https://doi.org/10.3390/cells9041019