Suppr超能文献

实时荧光成像引导溶瘤病毒治疗精确癌症治疗。

Real-Time Fluorescence Image-Guided Oncolytic Virotherapy for Precise Cancer Treatment.

机构信息

Department of Gastroenterological Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama 700-8558, Japan.

Center for Graduate Medical Education, Okayama University Hospital, Okayama 700-8558, Japan.

出版信息

Int J Mol Sci. 2021 Jan 17;22(2):879. doi: 10.3390/ijms22020879.

Abstract

Oncolytic virotherapy is one of the most promising, emerging cancer therapeutics. We generated three types of telomerase-specific replication-competent oncolytic adenovirus: OBP-301; a green fluorescent protein (GFP)-expressing adenovirus, OBP-401; and Killer-Red-armed OBP-301. These oncolytic adenoviruses are driven by the human telomerase reverse transcriptase (hTERT) promoter; therefore, they conditionally replicate preferentially in cancer cells. Fluorescence imaging enables visualization of invasion and metastasis in vivo at the subcellular level; including molecular dynamics of cancer cells, resulting in greater precision therapy. In the present review, we focused on fluorescence imaging applications to develop precision targeting for oncolytic virotherapy. Cell-cycle imaging with the fluorescence ubiquitination cell cycle indicator (FUCCI) demonstrated that combination therapy of an oncolytic adenovirus and a cytotoxic agent could precisely target quiescent, chemoresistant cancer stem cells (CSCs) based on decoying the cancer cells to cycle to S-phase by viral treatment, thereby rendering them chemosensitive. Non-invasive fluorescence imaging demonstrated that complete tumor resection with a precise margin, preservation of function, and prevention of distant metastasis, was achieved with fluorescence-guided surgery (FGS) with a GFP-reporter adenovirus. A combination of fluorescence imaging and laser ablation using a KillerRed-protein reporter adenovirus resulted in effective photodynamic cancer therapy (PDT). Thus, imaging technology and the designer oncolytic adenoviruses may have clinical potential for precise cancer targeting by indicating the optimal time for administering therapeutic agents; accurate surgical guidance for complete resection of tumors; and precise targeted cancer-specific photosensitization.

摘要

溶瘤病毒治疗是最有前途的新兴癌症治疗方法之一。我们生成了三种端粒酶特异性复制型溶瘤腺病毒:OBP-301;一种绿色荧光蛋白(GFP)表达腺病毒,OBP-401;和 Killer-Red 武装的 OBP-301。这些溶瘤腺病毒由人端粒酶逆转录酶(hTERT)启动子驱动;因此,它们在癌细胞中优先条件性复制。荧光成像能够在亚细胞水平上可视化体内的侵袭和转移;包括癌细胞的分子动力学,从而实现更精确的治疗。在本综述中,我们重点介绍了荧光成像在开发溶瘤病毒治疗的精准靶向中的应用。荧光泛素细胞周期指示剂(FUCCI)的细胞周期成像表明,溶瘤腺病毒和细胞毒性药物的联合治疗可以通过病毒治疗诱使静止的、化疗耐药的癌症干细胞(CSC)进入 S 期,从而使它们对化疗敏感,从而精确靶向静止的、化疗耐药的 CSC。非侵入性荧光成像表明,使用 GFP 报告腺病毒进行荧光引导手术(FGS)可以实现精确的肿瘤边缘完全切除、保留功能和预防远处转移。使用 KillerRed 蛋白报告腺病毒进行荧光成像和激光消融的组合导致有效的光动力癌症治疗(PDT)。因此,成像技术和设计的溶瘤腺病毒可能具有通过指示给予治疗剂的最佳时间、为肿瘤完全切除提供精确的手术指导以及精确的针对特定癌症的光敏化来实现精确癌症靶向的临床潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4527/7830621/901deef68469/ijms-22-00879-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验