CD81 通过阻断 CD274/PD-L1 的选择性自噬降解驱动放射抵抗性胶质母细胞瘤的免疫逃逸
CD81 drives immune evasion in radioresistant glioblastoma by blocking selective autophagic degradation of CD274/PD-L1.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Oncolytic virotherapy improves immunotherapies targeting cancer stemness in glioblastoma.
Oncolytic virotherapy improves immunotherapies targeting cancer stemness in glioblastoma.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
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。
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.
MEMBER ACCOUNT
登录成功会直接打开下一页。