4级弥漫性胶质瘤中Tim-3和Rel-B表达的临床病理及预后意义。

Fatih Yilmaz, Evrim Yilmaz, Deniz Arik, Funda Canaz, Bulent Yildiz, Melek Akcay, Emre Ozkara, Cengiz Bal
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引用次数: 0

摘要

目的:本研究旨在探讨免疫检查点分子Tim-3和NF-κB亚基Rel-B在4级弥漫性胶质瘤样本中的临床病理和预后意义及其相互关系。材料和方法:回顾并记录2016年至2019年间诊断为4级弥漫性胶质瘤患者的人口学、放射学、预后和治疗数据。免疫组化法将Tim-3和Rel-B分别应用于石蜡包埋组织。将Tim-3的表达分为免疫反应密度评分(IDS) (Low, High)和表达百分比(12%,12%),Rel-B的表达分为阳性和阴性组。结果:检出4级弥漫性胶质瘤99例,其中IDH-1阳性8例。Tim-3仅在肿瘤组织周围和内部的免疫细胞中表达,并且仅在带有Rel-B的肿瘤细胞中表达。IDH-1阳性患者Tim-3 IDS水平较低(中位数为31.8),而IDH-1阴性患者Tim-3 IDS水平较高(中位数为158)(p=0.020)。Tim-3 IDS高组与Rel-B阳性呈显著相关(p=0.007)。在IDH-1阴性队列中,单因素分析显示较高的Tim-3表达百分比和较高的IDS与较好的总生存期(OS) (p=0.041和p=0.042)和无进展生存期(PFS) (p=0.023和p=0.029)相关,而在多因素分析中,较高的Tim-3表达百分比被发现是较好的OS (p=0.008)和PFS (p=0.022)的独立预测因子。Rel-B阳性患者的OS和PFS较长,但差异无统计学意义(p 0.05)。结论:Tim-3可能是一个很好的预后预测因子和候选治疗方法,特别是在IDH-1阴性的4级弥漫性胶质瘤患者中,然而,Rel-B需要更多病例的进一步研究。Tim-3和Rel-B表达之间的显著关系支持NF-κB与免疫检查点通路之间的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinicopathological and Prognostic Significance of Tim-3 and Rel-B Expressions in Grade 4 Diffuse Gliomas.

Aim: To assess the clinicopathological and prognostic significance of Tim-3, an immune checkpoint molecule, and Rel-B, an NF-?B subunit, in grade 4 diffuse glioma samples and their relationship with each other.

Material and methods: The demographic, radiologic, treatment, and prognostic data of patients diagnosed with grade 4 diffuse glioma between 2016 and 2019 were reviewed and recorded. Tim-3 and Rel-B were applied to the paraffin-embedded tissues by immunohistochemistry method. Tim-3 expression was grouped as immunoreactivity density score (IDS) (Low, High) and expression percentage ( < 12%, > 12%), while Rel-B expression was divided into positive and negative groups.

Results: Ninety-nine grade 4 diffuse glioma samples were detected, 8 of which were IDH-1 positive. Tim-3 was expressed only in immune cells around and inside the tumoral tissue, and expression was detected only in tumoral cells with Rel-B. Tim-3 IDS was found at lower levels (median 31.8) in IDH-1 positive cases and higher (median 158) in IDH-1 negative ones (p=0.020). A significant correlation was found between the Tim-3 IDS high group and Rel-B positivity (p=0.007). In the IDH-1 negative cohort, the univariate analysis revealed higher Tim-3 expression percentage and higher IDS were associated with better overall survival (OS) (p=0.041 and p=0.042 respectively) and progression-free survival (PFS) (p=0.023 and p=0.029 respectively), while in the multivariate analysis higher Tim-3 expression percentage was found to be an independent predictor for better OS (p=0.008) and PFS (p=0.022). Rel-B positive cases exhibited longer OS and PFS but the result was not statistically significant (p > 0.05).

Conclusion: Tim-3 can be a good prognostic predictor and treatment candidate, especially in patients with IDH-1 negative grade 4 diffuse gliomas however, further studies with more cases are needed for Rel-B. The significant relationship between Tim-3 and Rel-B expressions supported the interaction between NF-?B and immune checkpoint pathways.

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