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针对小细胞肺癌的 DLL3 近红外光免疫疗法。

Near infrared photoimmunotherapy targeting DLL3 for small cell lung cancer.

机构信息

Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan.

Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan; S-YLC, Nagoya University Institute for Advanced Research, Japan; B3-Unit, Advanced Analytical and Diagnostic Imaging Center (AADIC)/Medical Engineering Unit (MEU), Nagoya University Institute for Advanced Research, Japan.

出版信息

EBioMedicine. 2020 Feb;52:102632. doi: 10.1016/j.ebiom.2020.102632. Epub 2020 Jan 23.

Abstract

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.

FUNDING

Research supported by grants from the Program for Developing Next-generation Researchers (Japan Science and Technology Agency), KAKEN (18K15923, JSPS), Medical Research Encouragement Prize of The Japan Medical Association, The Nitto Foundation, Kanae Foundation for the Promotion of Medical Science.

摘要

背景

小细胞肺癌(SCLC)预后较差,治疗选择有限。Delta 样蛋白 3(DLL3)特异性表达于 SCLC,被认为是该病患者有希望的治疗靶点。Rovalpituzumab tesirine(Rova-T)是首个靶向 DLL3 的抗体药物偶联物。尽管 Rova-T 的开发不幸终止,但 DLL3 仍然是 SCLC 的理想靶点。近红外光免疫治疗(NIR-PIT)是一种新的癌症治疗形式,它使用抗体-光敏剂偶联物,然后暴露于近红外光下,特异性地损伤靶细胞。在本研究中,我们展示了针对 DLL3 的近红外光免疫治疗,以开发针对 SCLC 的新型分子靶向治疗方法。

方法

将抗 DLL3 单克隆抗体 rovalpituzumab 与 IR700 光敏剂(称为“rova-IR700”)偶联。用 rova-IR700 孵育过表达 DLL3 的 SCLC 细胞以及非 DLL3 表达对照细胞,然后暴露于近红外光下。接下来,用 rova-IR700 注射 SCLC 异种移植小鼠,并用近红外光照射。

结果

DLL3 过表达细胞在近红外光照射下立即被破坏,而对照细胞保持完整。用 rova-IR700 和近红外光治疗的异种移植小鼠的肿瘤明显缩小,而单独注射 rova-IR700 或近红外光照射均未影响肿瘤大小。

结论

我们的数据表明,使用 NIR-PIT 靶向 DLL3 可能是一种治疗 SCLC 的新的有前途的方法。

资助

本研究得到日本科学技术振兴机构(JST)下一代研究人员培养计划(Program for Developing Next-generation Researchers)、日本学术振兴会(JSPS)科研费(18K15923)、日本医师协会医学研究鼓励奖、日本塩野义制药公司研究基金、公益财团法人仁科纪念癌研究财团的资助。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a9a/6992936/a0a727504a87/gr1.jpg

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