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基质免疫细胞中Siglec-15的表达与较低的膀胱肿瘤分期及较好的膀胱癌预后相关。

Stromal immune cells expression of Siglec-15 is associated with lower T stage and better prognosis of urinary bladder cancer.

作者信息

Chu Chengbiao, Fu Yao, Yang Jun, Fan Xiangshan, Shi Jiong

机构信息

Department of Pathology, Nanjing Drum Tower Hospital, Nanjing, China.

出版信息

Front Oncol. 2024 Dec 18;14:1437006. doi: 10.3389/fonc.2024.1437006. eCollection 2024.

Abstract

INTRODUCTION

Sialic acid-binding immunoglobulin-like lectin 15 (Siglec-15) is a novel immune checkpoint, similar to programmed death-ligand (PD-L1), and has emerged as a potential target for cancer immunotherapy. Until recently, little was known about the expression and role of Siglec-15 in bladder cancer (BC).

METHODS

In this study, we used immunohistochemical staining to assess the expression of Siglec-15 and PD-L1 in 69 primary BC samples and analyzed their relationship with clinicopathologic characters and prognosis.

RESULTS

The expression rates of Siglec-15 in the tumor cells, stromal immune cells, and both the tumor and stromal cells were 84.1% (58/69), 50.7% (35/69), and 44.9% (31/69), respectively. The PD-L1 expression rate was 52.2% (36/69), with a positive rate of 17.4% (12/69). PD-L1 expression was inversely correlated with Siglec-15 expression, but the statistical significance was not achieved ( = 0.072). Low stromal Siglec-15 expression was associated with advanced tumor stage ( = 0.010). PD-L1 expression was associated with tumor stage ( = 0.008) and perineural invasion (PNI) ( = 0.048). Kaplan-Meier survival curves showed that stromal Siglec-15 expression was associated with a better prognosis ( = 0.012), although it was not an independent prognostic factor after multivariate analysis ( = 0.236) .

DISCUSSION

This study revealed a high expression rate of Siglec-15 in BC and may provide valuable insights for patient selection in future clinical trials.

摘要

引言

唾液酸结合免疫球蛋白样凝集素15(Siglec-15)是一种新型免疫检查点,类似于程序性死亡配体(PD-L1),已成为癌症免疫治疗的潜在靶点。直到最近,关于Siglec-15在膀胱癌(BC)中的表达和作用仍知之甚少。

方法

在本研究中,我们使用免疫组织化学染色评估了69例原发性BC样本中Siglec-15和PD-L1的表达,并分析了它们与临床病理特征和预后的关系。

结果

Siglec-15在肿瘤细胞、基质免疫细胞以及肿瘤和基质细胞中的表达率分别为84.1%(58/69)、50.7%(35/69)和44.9%(31/69)。PD-L1表达率为52.2%(36/69),阳性率为17.4%(12/69)。PD-L1表达与Siglec-15表达呈负相关,但未达到统计学意义(P = 0.072)。基质Siglec-15低表达与肿瘤晚期相关(P = 0.010)。PD-L1表达与肿瘤分期(P = 0.008)和神经周围浸润(PNI)(P = 0.048)相关。Kaplan-Meier生存曲线显示,基质Siglec-15表达与较好的预后相关(P = 0.012),尽管在多因素分析后它不是独立的预后因素(P = 0.236)。

讨论

本研究揭示了Siglec-15在BC中的高表达率,并可能为未来临床试验中的患者选择提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f663/11688221/5e65c9543ee3/fonc-14-1437006-g001.jpg

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