肿瘤微环境生物标志物与胃肠道外间质瘤的增殖活性和免疫反应相关:探索不同年龄组的差异。

Valentin Tiberiu Moldovan, María Sajin, Leila Ali
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引用次数: 0

摘要

导言:胃肠道外间质瘤(EGISTs)是起源于卡贾尔样细胞的非胃肠道肉瘤。最近的研究表明,肿瘤微环境至关重要,并强调了瘤内白细胞群在恶性肿瘤中的重要性,这极大地影响了EGISTs的治疗策略:本研究旨在描述 EGISTs 肿瘤内白细胞群的特征,将增殖指数(ki67)与白细胞密度相关联,并研究年龄对增殖活性和免疫反应的影响:我们对 2007 年 1 月至 2020 年 6 月期间在 "维克多-巴贝斯 "国家病理研究所和布加勒斯特大学急诊医院就诊的 25 名 EGIST 患者进行了回顾性分析。在排除了5名患者后,共有19名患者纳入了本研究。免疫组化利用 CD5、CD20、CD45 和 ki67 抗体识别和评估瘤内淋巴细胞,并通过 QuPath 软件进行分析。统计分析包括Pearson相关性、Kruskal-Wallis检验和Bonferroni校正:结果:确诊为EGIST的患者平均年龄为51岁;不同形态类型的患者ki67表达各不相同。免疫组化显示了不同的肿瘤浸润淋巴细胞(TIL)密度,ki67与TIL-CD05/CD20阳性细胞之间存在显著关联。研究还发现了与年龄有关的相关性,这凸显了肿瘤微环境的复杂性:我们的研究结果强调了免疫微环境在 EGIST 中的作用,显示了 ki67 表达和 TIL 密度之间的显著相关性以及与年龄相关的关联性。这项研究加深了我们对 EGIST 病理生理学的理解,有助于我们进一步探索更好的治疗方法,并全面了解 EGISTs 的免疫反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumor Microenvironment Biomarkers Correlated with Proliferative Activity and Immune Response in Extragastrointestinal Stromal Tumors: Exploring Variations in Different Age Groups.

Introduction: Extra-gastrointestinal stromal tumors (EGISTs) are non-gastrointestinal sarcomas originating from Cajal-like cells. Recent studies show the tumor microenvironment is crucial and highlight the importance of intra-tumoral leukocyte populations in malignancies, which are greatly impacting treatment strategies in EGISTs.

Aim and objectives: This study aims to characterize intra-tumoral leukocyte populations in EGISTs, correlating proliferative index (ki67) with leukocyte density and examining age-related effects on proliferative activity and immune response.

Methods: We conducted a retrospective analysis on 25 patients with EGIST who came at "Victor Babes" National Institute of Pathology and Bucharest University Emergency Hospital between January 2007 and June 2020. After excluding five patients, a total of 19 subjects were included in the present study. Immunohistochemistry utilizing CD5, CD20, CD45 and ki67 antibodies identified and assessed intratumoral lymphocytes, analyzed via QuPath software. Statistical analyses included Pearson correlation, Kruskal-Wallis tests and Bonferroni corrections.

Results: The mean age of patients diagnosed with EGIST was 51 years; ki67 expression varied among morphological types. Immunohistochemistry revealed distinct tumor-infiltrating lymphocytes (TIL) densities with significant associations between ki67 and TIL-CD05/CD20 positive cells. Age-related correlations were noted, which highlighted complexities within the tumor microenvironment.

Conclusion: Our findings emphasize the role of the immune microenvironment in EGISTs, showing significant correlations between ki67 expression and TIL densities as well as age-related associations. This study enhances our understanding of EGIST pathophysiology, urging further exploration for improved therapeutic approaches and comprehensive insights into immune responses in EGISTs.

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