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溶瘤病毒疗法改善靶向胶质母细胞瘤肿瘤干性的免疫疗法

英文原题:Oncolytic virotherapy improves immunotherapies targeting cancer stemness in glioblastoma.

查看英文原题

Oncolytic virotherapy improves immunotherapies targeting cancer stemness in glioblastoma.

PubMed 2024/06/18(内容时间) Biochim Biophys Acta Gen Subj Q2 · IF 2.9(JCR 2025)

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中文摘要

尽管癌症治疗取得了进展,胶质母细胞瘤(GBM)仍然是中枢神经系统中最具耐药性和复发性的肿瘤。GBM 肿瘤微环境(TME)是一个高度动态的景观,与肿瘤浸润细胞的变化一致,在肿瘤进展和侵袭中发挥关键作用。此外,具有自我更新能力的胶质瘤干细胞(GSCs)促进肿瘤复发并诱导治疗耐药,这些都使得现有疗法难以彻底根除 GBM。溶瘤病毒治疗是一个有前景的治疗领域,能够以靶向方式杀伤肿瘤细胞。经过改造的溶瘤病毒(OVs)通过直接裂解肿瘤细胞、浸润抗肿瘤细胞、诱导免疫原性细胞死亡,以及将免疫耐受的 TME 致敏为免疫响应的热状态,从而改善癌症免疫治疗。重要的是,OVs 可以靶向干细胞驱动的 GBM 进展。在这篇综述中,我们将讨论 OVs 作为一种治疗选择如何靶向 GBM,尤其是 GSC 亚群,并诱导免疫原性以重塑 TME,进而增强免疫治疗的效率。

展开英文摘要原文

Despite advances in cancer therapies, glioblastoma (GBM) remains the most resistant and recurrent tumor in the central nervous system. GBM tumor microenvironment (TME) is a highly dynamic landscape consistent with alteration in tumor infiltration cells, playing a critical role in tumor progression and invasion.

In addition, glioma stem cells (GSCs) with self-renewal capability promote tumor recurrence and induce therapy resistance, which all have complicated eradication of GBM with existing therapies. Oncolytic virotherapy is a promising field of therapy that can kill tumor cells in a targeted manner. Manipulated oncolytic viruses (OVs) improve cancer immunotherapy by directly lysis tumor cells, infiltrating antitumor cells, inducing immunogenic cell death, and sensitizing immune-resistant TME to an immune-responsive hot state.

Importantly, OVs can target stemness-driven GBM progression. In this review, we will discuss how OVs as a therapeutic option target GBM, especially the GSC subpopulation, and induce immunogenicity to remodel the TME, which subsequently enhances immunotherapies' efficiency.

论文信息

作者
Keshavarz M、Dianat-Moghadam H、Ghorbanhosseini SS、Sarshari B
第一作者单位
Department of Medical Virology, The Persian Gulf Tropical Medicine Research Center, The Persian Gulf Biomedical Sciences Research Institute, Bushehr University of Medical Sciences, Bushehr, Iran. Electronic address: keshavarz.m@bpums.ac.ir.Iran
通讯作者单位
Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan 8174673461, Iran; Pediatric Inherited Diseases Research Center, Isfahan University of Medical Sciences, Isfahan 8174673461, Iran. Electronic address: Dianat.h@med.mui.ac.ir.Iran
文献类型
综述
期刊
Biochimica et biophysica acta. General subjects2024 Sep
原文标识
PubMed 38901497 · DOI 10.1016/j.bbagen.2024.130662