TY - JOUR
T1 - Targeted Phototherapy for Malignant Pleural Mesothelioma
T2 - Near-Infrared Photoimmunotherapy Targeting Podoplanin
AU - Nishinaga, Yuko
AU - Sato, Kazuhide
AU - Yasui, Hirotoshi
AU - Taki, Shunichi
AU - Takahashi, Kazuomi
AU - Shimizu, Misae
AU - Endo, Rena
AU - Koike, Chiaki
AU - Kuramoto, Noriko
AU - Nakamura, Shota
AU - Fukui, Takayuki
AU - Yukawa, Hiroshi
AU - Baba, Yoshinobu
AU - K Kaneko, Mika
AU - Chen-Yoshikawa, Toyofumi F.
AU - Kobayashi, Hisataka
AU - Kato, Yukinari
AU - Hasegawa, Yoshinori
PY - 2020/4/20
Y1 - 2020/4/20
N2 - 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.
AB - 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.
KW - malignant pleural mesothelioma
KW - near-infrared photoimmunotherapy
KW - podoplanin (PDPN)
UR - http://www.scopus.com/inward/record.url?scp=85084030978&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85084030978&partnerID=8YFLogxK
U2 - 10.3390/cells9041019
DO - 10.3390/cells9041019
M3 - Article
C2 - 32326079
AN - SCOPUS:85084030978
SN - 2073-4409
VL - 9
JO - Cells
JF - Cells
IS - 4
ER -