Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
Department of General Surgery, Zhongshan Hospital, Fudan University, Shanghai, China.
Br J Cancer. 2022 Jan;126(1):100-108. doi: 10.1038/s41416-021-01607-3. Epub 2021 Nov 1.
T cell immunoglobulin and mucin domain-containing protein 3 (TIM3) is a crucial immune checkpoint and is considered as an emerging target for cancer treatment. However, the clinical significance and immune-related role of TIM3 cells in gastric cancer remain unknown. This study aimed to investigate the clinical significance of tumour-infiltrating TIM3 cells and their association with immune contexture in gastric cancer.
This study enrolled three cohorts, including 436 tumour tissue microarray specimens and 58 fresh tumour tissues of gastric cancer patients from Zhongshan Hospital, and 330 transcriptional data from The Cancer Genome Atlas. TIM3 cells and their association with CD8 T cells were evaluated by immunohistochemistry and flow cytometry analyses. Kaplan-Meier curves, Cox model and interaction test were performed to assess clinical outcomes.
Tumour-infiltrating TIM3 cells' high subgroups experienced poorer overall survival and disease-free survival and predicted inferior therapeutic responsiveness to fluorouracil-based adjuvant chemotherapy. TIM3 indicated CD8 T cell dysfunction, which impeded chemotherapeutic responsiveness. Besides, HAVCR2 messenger RNA expression was associated with specific molecular characteristics.
The abundance of tumour-infiltrating TIM3 cells could identify an immunoevasive subtype gastric cancer with CD8 T cell dysfunction, suggesting that TIM3 might serve as a promising target for immunotherapy in gastric cancer.
T 细胞免疫球蛋白和粘蛋白结构域蛋白 3(TIM3)是一种重要的免疫检查点,被认为是癌症治疗的新兴靶点。然而,TIM3 细胞在胃癌中的临床意义和免疫相关作用尚不清楚。本研究旨在探讨肿瘤浸润 TIM3 细胞的临床意义及其与胃癌免疫结构的关系。
本研究纳入了三个队列,包括来自中山医院的 436 例肿瘤组织微阵列标本和 58 例胃癌患者的新鲜肿瘤组织,以及来自癌症基因组图谱的 330 个转录组数据。通过免疫组织化学和流式细胞术分析评估 TIM3 细胞及其与 CD8 T 细胞的相关性。采用 Kaplan-Meier 曲线、Cox 模型和交互检验评估临床结局。
肿瘤浸润 TIM3 细胞高亚组的总生存期和无病生存期较差,且对氟尿嘧啶为基础的辅助化疗反应性较差。TIM3 提示 CD8 T 细胞功能障碍,阻碍了化疗的反应性。此外,HAVCR2 信使 RNA 的表达与特定的分子特征相关。
肿瘤浸润 TIM3 细胞的丰度可以识别出具有 CD8 T 细胞功能障碍的免疫逃避型胃癌,提示 TIM3 可能成为胃癌免疫治疗的有前途的靶点。