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Tim-3 和 PD-1 表达在上尿路尿路上皮癌预后中的预后和临床病理学意义

英文原题:The prognostic and clinicopathological significance of Tim-3 and PD-1 expression in the prognosis of upper urinary tract urothelial carcinoma.

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The prognostic and clinicopathological significance of Tim-3 and PD-1 expression in the prognosis of upper urinary tract urothelial carcinoma.

PubMed 2021/07/28(内容时间) Urol Oncol Q2 · IF 2.8(JCR 2025)

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研究概要

我们证实,Tim-3 蛋白高表达可作为 UTUC 患者较早发生 IVR 和较短 OS 的指标,而 PD-1 高表达仅与较早发生 IVR 相关。我们发现,Tim-3 在肿瘤复发和进展中的作用比 PD-1 更重要。总体而言,我们的研究结果支持将 Tim-3 和 PD-1 作为提示患者生存不良的临床预后因素。Tim-3 单独或与 PD-1 联合,可能成为未来 UTUC 治疗的靶点,但仍需进一步的前瞻性研究。

研究思路结论见上方概要

上尿路尿路上皮癌(UTUC)是一种相对少见的疾病,报道的分子标志物很少。本研究评估了原发性UTUC中Tim-3和PD-1的表达及其对患者临床结局的影响。

采用免疫组化法检测101例UTUC患者石蜡包埋切片中Tim-3和PD-1蛋白的表达。H-score与临床病理结局及长期复发率和生存率进行相关性分析。

T细胞免疫球蛋白黏蛋白-3(Tim-3)蛋白在UTUC细胞中过表达,尤其是在TIL(肿瘤浸润淋巴细胞)(TILs)和内皮细胞中。我们发现95%(95/101)的UTUC组织存在Tim-3表达失调,其中44%(44/101)显示高表达。Tim-3高表达(H-score≥100)与晚期病理分级、晚期T分期和肿瘤复发显著相关(P=0.016、0.001和<0.001),并与较差的膀胱内无复发生存期(IRFS)和总生存期(OS)相关(P<0.001和0.003)。此外,本研究还评估了另一种免疫检查点分子——程序性死亡受体-1(PD-1)。在Tim-3低表达亚组患者中,PD-1高表达者比PD-1低表达者更常发生膀胱内复发(IVR)(P<0.001)。然而,在Tim-3高表达亚组中,PD-1表达水平对预后无影响。

展开英文摘要原文

Upper urinary tract urothelial carcinoma (UTUC) is a relatively uncommon disease with few reported molecular markers. This study evaluated Tim-3 and PD-1 expression in primary UTUC and its impact on patients' clinical outcomes.

Tim-3 and PD-1 protein expression was detected by immunohistochemistry in paraffin-embedded sections from 101 UTUC patients. The H-score was correlated with clinicopathologic outcomes and the long-term recurrence and survival rates.

T cell immunoglobulin mucin-3 (Tim-3) protein was overexpressed in UTUC cells, especially tumour-infiltrating lymphocytes (TILs) and endothelial cells. We found that 95% (95/101) of UTUC tissues had dysregulated Tim-3 expression, of which 44% (44/101) showed high expression. High Tim-3 expression (H-score≥100) was significantly correlated with advanced pathological grade, advanced T stage and tumour recurrence (P=0.016, 0.001 and < 0.001, respectively) and with poor intravesical recurrence-free survival (IRFS) and overall survival (OS) (P< 0.001 and 0.003). Moreover, another immune checkpoint molecule, programmed death receptor-1 (PD-1), was also assessed in our study. Among patients in the low Tim-3 expression subgroup, those with high PD-1 expression experienced intravesical recurrence (IVR) more often than those with low PD-1 expression (P< 0.001). However, the PD-1 expression level had no effect on prognosis in the high Tim-3 expression subgroup.

We confirmed that high Tim-3 protein expression can be used as an indicator of earlier IVR and shorter OS in patients with UTUC, while high expression of PD-1 is only related to earlier IVR. We showed that Tim-3 plays a more important role in tumour recurrence and progression than PD-1. Collectively, our findings support the use of Tim-3 and PD-1 as clinical prognostic factors indicating poor patient survival. Tim-3, alone or in combination with PD-1, could become a target for future UTUC therapies, but further prospective studies are needed.

论文信息

作者
Chen H、Wang M、Weng T、Wei Y、Liu C、Yang L、Ren K、Tang Y
第一作者单位
Department of Urology, Chengdu Second People's Hospital (Chengdu Third Clinical College Affiliated to Chongqing Medical University), Chengdu, China.China
通讯作者单位
Department of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China. Electronic address: wangm20201028@163.com.China
文献类型
综述
期刊
Urologic oncology2021 Nov
原文标识
PubMed 34330653 · DOI 10.1016/j.urolonc.2021.05.039