更正:B7-H3 CAR T 细胞清除肝内胆管癌并诱导持久应答
Correction: B7-H3 CAR T cells eradicate intrahepatic cholangiocarcinoma and induce durable response.
英文原题:Cancer-associated fibroblast senescence and its relation with tumour-infiltrating lymphocytes and PD-L1 expressions in intrahepatic cholangiocarcinoma.
以 CAV1 水平为代表的细胞衰老,可能是 CAF 的标志物,并通过 Foxp3+ TIL 调控成为 ICC 的预后指标。
背景:癌症相关成纤维细胞(CAF)中的小窝蛋白1(CAV1)可根据癌症类型发挥促癌或抑癌作用。然而,其在肝内胆管癌(ICC)中的作用尚不明确。因此,本研究旨在探究ICC患者CAF中的CAV1与TIL(肿瘤浸润淋巴细胞)数量或PD-L1水平之间的关系。方法:连续纳入158例ICC患者。采用免疫组化分析CAF中CAV1、CD8+ TIL、Foxp3+ TIL以及癌细胞中的PD-L1水平,并评估其与临床病理因素和预后的关系,以及这些因素之间的相关性。结果:CAF中CAV1上调与总生存期(OS)较差(P<0.001)和无复发生存期较差(P=0.008)相关。临床病理因素与CA19-9高水平(P<0.001)、肿瘤分期较晚(P=0.046)和淋巴结转移(P=0.004)相关。CAV1水平与Foxp3+ TIL数量呈正相关(P=0.01)。CAV1水平与CD8+ TIL数量(P=0.80)及PD-L1水平(P=0.97)均无显著相关性。CD8+ TIL数量增加、Foxp3+ TIL数量减少与OS延长相关。多变量分析中,CAF内CAV1阳性表达(P=0.013)及CD8+ TIL数量减少(P=0.021)均为独立不良预后因素。结论:以CAV1水平代表的细胞衰老可能是CAF的标志物,并可通过调节Foxp3+ TIL成为ICC预后指标。CAF中的CAV1表达可能是ICC的治疗靶点。
BACKGROUND: Caveolin-1 (CAV1) in cancer-associated fibroblasts (CAFs) has pro- or anti-tumourigenic effect depending on the cancer type. However, its effect in intrahepatic carcinoma (ICC) remains unknown. Therefore, this study aimed to investigate the relationship between CAV1 in CAFs and tumour-infiltrating lymphocyte (TIL) numbers or PD-L1 levels in ICC patients. METHODS: Consecutive ICC patients (n = 158) were enrolled in this study. The levels of CAV1 in CAFs, CD8 + TILs, Foxp3+ TILs and PD-L1 in cancer cells were analysed using immunohistochemistry. Their association with the clinicopathological factors and prognosis were evaluated. The correlation between these factors was evaluated. RESULTS: CAV1 upregulation in CAFs was associated with a poor overall survival (OS) (P < 0.001) and recurrence-free survival (P = 0.008). Clinicopathological factors were associated with high CA19-9 levels (P < 0.001), advanced tumour stage (P = 0.046) and lymph node metastasis (P = 0.004). CAV1 level was positively correlated with Foxp3+ TIL numbers (P = 0.01). There were no significant correlations between CAV1 levels and CD8 + TIL numbers (P = 0.80) and PD-L1 levels (P = 0.97). An increased CD8 + TIL number and decreased Foxp3+ TIL number were associated with an increased OS. In multivariate analysis, positive CAV1 expression in CAFs (P = 0.013) and decreased CD8 + TIL numbers (P = 0.021) were independent poor prognostic factors. CONCLUSION: Cellular senescence, represented by CAV1 levels, may be a marker of CAFs and a prognostic indicator of ICC through Foxp3+ TIL regulation. CAV1 expression in CAFs can be a therapeutic target for ICC.
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