Near infrared photoimmunotherapy targeting DLL3 for small cell lung cancer

被引:59
作者
Isobe, Yoshitaka [1 ]
Sato, Kazuhide [1 ,2 ,3 ]
Nishinaga, Yuko [1 ]
Takahashi, Kazuomi [1 ]
Taki, Shunichi [1 ]
Yasui, Hirotoshi [1 ]
Shimizu, Misae [1 ,3 ]
Endo, Rena [1 ,3 ]
Koike, Chiaki [1 ,3 ]
Kuramoto, Noriko [3 ]
Yukawa, Hiroshi [3 ,4 ,5 ]
Nakamura, Shota [6 ]
Fukui, Takayuki [6 ]
Kawaguchi, Koji [6 ]
Chen-Yoshikawa, Toyofumi F. [6 ]
Baba, Yoshinobu [4 ,5 ]
Hasegawa, Yoshinori [7 ]
机构
[1] Nagoya Univ, Dept Resp Med, Grad Sch Med, Nagoya, Aichi 4668550, Japan
[2] Nagoya Univ, S YLC, Inst Adv Res, Nagoya, Aichi, Japan
[3] Nagoya Univ, AADIC, B3 Unit, Inst Adv Res,MEU, Nagoya, Aichi, Japan
[4] Nagoya Univ, Inst Innovat Future Soc, Inst Nanolife Syst, Nagoya, Aichi, Japan
[5] Nagoya Univ, Dept Biomol Engn, Grad Sch Engn, Nagoya, Aichi, Japan
[6] Nagoya Univ, Dept Thorac Surg, Grad Sch Med, Nagoya, Aichi, Japan
[7] Natl Hosp Org, Nagoya Med Ctr, Nagoya, Aichi, Japan
基金
日本科学技术振兴机构;
关键词
Photoimmunotherapy; DLL3; Small cell lung cancer; Bioluminescence; In vivo imaging; MONOCLONAL-ANTIBODIES; IN-VIVO; ESTABLISHMENT; EXPRESSION;
D O I
10.1016/j.ebiom.2020.102632
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Small cell lung cancer (SCLC) has a poor prognosis, and its treatment options are limited. Delta-like protein 3 (DLL3) is expressed specifically in SCLC and is considered a promising therapeutic target for patients with this disease. Rovalpituzumab tesirine (Rova-T) was the first antibody-drug conjugate targeting DLL3. Although Rova-T development was unfortunately terminated, DLL3 remains an ideal target for SCLC. Near infrared photoimmunotherapy (NIR-PIT) is a new form of cancer treatment that employs an antibody-photosensitiser conjugate followed by NIR light exposure and damage target cells specifically. In this study, we demonstrate DLL3-targeted NIR-PIT to develop a novel molecularly targeted treatment for SCLC. Methods: The anti-DLL3 monoclonal antibody rovalpituzumab was conjugated to an IR700 photosensitiser (termed 'rova-IR700'). SCLC cells overexpressing DLL3 as well as non-DLL3-expressing controls were incubated with rova-IR700 and then exposed to NIR-light. Next, mice with SCLC xenografts were injected with rova-IR700 and irradiated with NIR-light. Findings: DLL3-overexpressing cells underwent immediate destruction upon NIR-light exposure, whereas the control cells remained intact. The xenograft in mice treated with rova-IR700 and NIR-light shrank markedly, whereas neither rova-IR700 injection nor NIR-light irradiation alone affected tumour size. Interpretation: Our data suggest that targeting of DLL3 using NIR-PIT could be a novel and promising treatment for SCLC. (C) 2020 The Authors. Published by Elsevier B.V.
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页数:12
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