单细胞追踪揭示黑色素瘤 TIL 治疗过程中肿瘤反应性 T 细胞的可塑性
Single-cell tracking reveals tumor-reactive T cell plasticity during melanoma TIL therapy.
TIL(肿瘤浸润淋巴细胞)过继细胞治疗可在转移性黑色素瘤中诱导持久缓解,然而在体外扩增过程中及回输后,调控肿瘤反应性T细胞命运的克隆和转录动态仍知之甚少。
英文原题:Exploring the role and mechanisms of MAGEA4 in tumorigenesis, regulation, and immunotherapy.
MAGEA4是黑色素瘤相关抗原(MAGE)家族的一员,其特征是在多种肿瘤组织中高表达,而在正常组织中低表达,但睾丸和胎盘除外。
MAGEA4是黑色素瘤相关抗原(MAGE)家族的一员,其特征是在多种肿瘤组织中高表达,而在正常组织中低表达,睾丸和胎盘除外。其表达与癌症的不良预后相关。本综述总结了MAGEA4在癌症中的作用机制、调控功能及免疫治疗应用。MAGEA4通过多种途径促进肿瘤的发生和发展,包括肿瘤抑制因子P53的泛素化降解、细胞周期和凋亡的调控、DNA损伤修复的调节以及癌细胞存活能力的增强。通过与TRIM28形成复合物,MAGEA4通过P53降解加速肿瘤发展。TWIST1和BORIS等因素可上调MAGEA4的表达。MAGEA4与Miz-1、p53和RAD18等蛋白相互作用,参与基因转录调控和DNA损伤修复。通过稳定RAD18,MAGEA4促进Y家族DNA聚合酶的招募,使细胞在DNA损伤条件下继续复制,从而支持癌细胞的存活。基于MAGEA4的TCR-T细胞疗法和癌症疫苗显示出临床潜力。本文全面综述了MAGEA4的结构和功能,以及在实体瘤中的最新研究进展,为MAGEA4的临床转化及其在免疫治疗中的应用提供了理论基础。
MAGEA4 is a member of the Melanoma-Associated Antigen (MAGE) family, characterized by high expression in various tumor tissues but low expression in normal tissues, with the exception of testis and placenta. Its expression is associated with poor prognosis in cancer. This review summarizes the mechanisms of action, regulatory functions, and immunotherapeutic applications of MAGEA4 in cancer.MAGEA4 promotes tumor initiation and progression through multiple pathways, including ubiquitination and degradation of the tumor suppressor P53, regulation of cell cycle and apoptosis, modulation of DNA damage repair, and enhancement of cancer cell survival. By forming a complex with TRIM28, MAGEA4 accelerates tumor development via P53 degradation. Factors such as TWIST1 and BORIS can upregulate MAGEA4 expression. MAGEA4 interacts with proteins including Miz-1, p53, and RAD18, participating in gene transcription regulation and DNA damage repair. By stabilizing RAD18, MAGEA4 facilitates the recruitment of Y-family DNA polymerases, enabling cells to continue replication under DNA damage conditions and thus supporting cancer cell survival. MAGEA4-based TCR-T cell therapy and cancer vaccines show clinical potential. This article comprehensively reviews the structure and function of MAGEA4, as well as recent research progress in solid tumors, providing a theoretical foundation for the clinical translation of MAGEA4 and its application in immunotherapy.
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