Cells (Apr 2020)

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

  • 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

DOI
https://doi.org/10.3390/cells9041019
Journal volume & issue
Vol. 9, no. 4
p. 1019

Abstract

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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 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.

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