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

被引:44
作者
Nishinaga, Yuko [1 ]
Sato, Kazuhide [1 ,2 ,3 ]
Yasui, Hirotoshi [1 ]
Taki, Shunichi [1 ]
Takahashi, Kazuomi [1 ]
Shimizu, Misae [1 ,2 ]
Endo, Rena [1 ,2 ]
Koike, Chiaki [1 ,2 ]
Kuramoto, Noriko [2 ]
Nakamura, Shota [4 ]
Fukui, Takayuki [4 ]
Yukawa, Hiroshi [2 ,5 ,6 ]
Baba, Yoshinobu [5 ,6 ]
Kaneko, Mika K. [7 ]
Chen-Yoshikawa, Toyofumi F. [4 ]
Kobayashi, Hisataka [8 ]
Kato, Yukinari [7 ,9 ]
Hasegawa, Yoshinori [10 ]
机构
[1] Nagoya Univ, Resp Med, Grad Sch Med, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, Inst Adv Res, Adv Analyt & Diagnost Imaging Ctr AADIC, Med Engn Unit MEU,Unit B3, Nagoya, Aichi 4668550, Japan
[3] Nagoya Univ, Inst Adv Res, SYLC, Nagoya, Aichi 4648601, Japan
[4] Nagoya Univ, Grad Sch Med, Dept Thorac Surg, Nagoya, Aichi 4668550, Japan
[5] Nagoya Univ, Inst Nanolife Syst, Inst Innovat Future Soc, Nagoya, Aichi 4648601, Japan
[6] Nagoya Univ, Dept Biomol Engn, Grad Sch Engn, Nagoya, Aichi 4648601, Japan
[7] Tohoku Univ, Dept Antibody Drug Dev, Grad Sch Med, Sendai, Miyagi 9808575, Japan
[8] NCI, Mol Imaging Program, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[9] Tohoku Univ, New Ind Creat Hatchery Ctr, Sendai, Miyagi 9808575, Japan
[10] Nagoya Med Ctr, Natl Hosp Org, Nagoya, Aichi 4600001, Japan
基金
日本科学技术振兴机构;
关键词
podoplanin (PDPN); near-infrared photoimmunotherapy; malignant pleural mesothelioma; OPTICAL IMAGING PROPERTIES; IN-VIVO; MONOCLONAL-ANTIBODIES; LUNG-CANCER; INHIBITION; EXPRESSION; SPREAD; CHARGE;
D O I
10.3390/cells9041019
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
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页数:17
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