Zhang Wentao, Ren Wen, Guo Shuyan, Han Haobo, Cai Weiwen, Bai Haowen, Li Long, Jiang Xiangyan, Zheng Xin, Zhang Tiansheng, Wang Yan, Ye Huili, Cao Hongtai, Shi Wengui, Zhou Huinian, Yu Zeyuan, Qin Long, Jiao Zuoyi
Cuiying Biomedical Research Center, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou, Gansu, China.
Department of General Surgery, The Second Hospital & Clinical Medical School, Lanzhou University, Gansu, China.
Cell Death Dis. 2025 Aug 8;16(1):597. doi: 10.1038/s41419-025-07905-5.
Gastric cancer (GC) is characterised by a dense stromal microenvironment, lack of therapeutic targets, and limited effective treatment options, collectively leading to a poor prognosis. Here, we identify UL16 binding protein 2 (ULBP2) as a potential therapeutic target in GC. Mechanistically, ULBP2 overexpression activates the TGF-β signalling pathway, promoting the activation of cancer-associated fibroblasts (CAFs) and tumor progression in GC. Furthermore, we developed ULBP2 CAR-T cells and assessed their therapeutic potential in GC cell lines, organoids, cell line-derived xenograft (CDX) and patient-derived xenograft (PDX) mouse models. We showed that ULBP2 CAR-T cells effectively eliminated GC cell lines and organoids and, either alone or in combination with an anti-PD-1 antibody, significantly inhibited tumor growth and prolonged survival in both CDX and PDX mouse models. In conclusion, ULBP2 contributes to GC progression by promoting TGF-β mediated CAF activation, which collectively reinforce the dense stromal microenvironment. Targeting ULBP2 suppresses tumor growth, reduces stromal deposition, and promotes T cell infiltration, thereby enhancing the efficacy of immunotherapy in GC.
胃癌(GC)的特征是存在致密的基质微环境、缺乏治疗靶点且有效治疗选择有限,这些因素共同导致预后不良。在此,我们确定UL16结合蛋白2(ULBP2)为胃癌的潜在治疗靶点。从机制上讲,ULBP2的过表达激活了转化生长因子-β(TGF-β)信号通路,促进了胃癌中癌相关成纤维细胞(CAF)的活化和肿瘤进展。此外,我们构建了ULBP2嵌合抗原受体T细胞(CAR-T),并在胃癌细胞系、类器官、细胞系来源的异种移植(CDX)和患者来源的异种移植(PDX)小鼠模型中评估了它们的治疗潜力。我们发现,ULBP2 CAR-T细胞有效地清除了胃癌细胞系和类器官,并且单独或与抗程序性死亡蛋白1(PD-1)抗体联合使用时,在CDX和PDX小鼠模型中均显著抑制了肿瘤生长并延长了生存期。总之,ULBP2通过促进TGF-β介导的CAF活化来促进胃癌进展,这共同强化了致密的基质微环境。靶向ULBP2可抑制肿瘤生长、减少基质沉积并促进T细胞浸润,从而增强胃癌免疫治疗的疗效。