成纤维细胞生长因子受体 (FGFR) 2 和 3 蛋白对浸润性尿路上皮膀胱癌的预后有影响吗?

Q3 Medicine
Iranian Journal of Pathology Pub Date : 2024-01-01 Epub Date: 2024-03-29 DOI:10.30699/IJP.2024.2012115.3180
Shereen Fathy Mahmoud, Nanis Shawky Holah, Alshimaa Mahmoud Alhanafy, Marwa Mohammed Serag El-Edien
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引用次数: 0

摘要

背景与目的:在埃及,膀胱癌在男性发病率中排名第二。作为酪氨酸激酶家族的一员,成纤维细胞生长因子受体(FGFR)失调与人类的一些恶性肿瘤有关。本研究旨在分析患者的临床病理数据,同时研究浸润性尿路上皮膀胱癌中 FGFR2 和 FGFR3 的免疫组化表达:这项回顾性横断面研究纳入了梅努菲亚大学医学院病理学系2009年至2020年的60例浸润性尿路上皮癌(UC)病例。所有活检组织均进行了表皮生长因子受体 2(FGFR2)和表皮生长因子受体 3(FGFR3)抗体染色。临床肿瘤科和核医学科对 44 例患者进行了治疗和随访,并获得了完整的临床数据:结果:晚期和高级别肿瘤与 FGFR2 阳性有明显相关性(P=0.048 和 0.044)。有硬脑膜周围侵犯的病例显示出更高的 FGFR2 阳性率(P=0.023)。FGFR3表达与淋巴结阳性之间存在明显的间接线性相关(r= -0.265,P=0.041):结论:FGFR2的高表达与不良预后参数相关,而FGFR3的高表达与良好预后参数相关。这些研究结果可能会突出表皮生长因子受体靶向治疗(表皮生长因子受体2拮抗剂和表皮生长因子受体3激动剂)对治疗尿路癌患者的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do Fibroblast Growth Factor Receptor (FGFR) 2 and 3 Proteins Play a Role in Prognosis of Invasive Urothelial Bladder Carcinoma?

Background & objective: Bladder carcinoma ranks second in prevalence among males in Egypt. As a family of tyrosine kinases, fibroblast growth factor receptor (FGFR) dysregulation has been linked to some malignancies in humans. The aim of this study is to analyze the clinicopathological data of patients while investigating FGFR2 and FGFR3 immunohistochemical expression in invasive urothelial bladder carcinoma.

Methods: This retrospective cross-sectional study included 60 invasive urothelial carcinoma (UC) cases in the Pathology department, Faculty of Medicine, Menoufia University, from 2009 to 2020. All biopsies were stained for FGFR2 and FGFR3 antibodies. Complete clinical data were available for 44 patients treated and followed in clinical oncology and nuclear medicine departments.

Results: Advanced stage and high grade are significantly correlated with FGFR2 positivity (P=0.048 and 0.044, respectively). Cases presented with Perineural invasion showed a higher percentage of FGFR2 (P=0.023). There is a significant indirect linear correlation between FGFR3 expression and lymph node positivity (r= -0.265, P=0.041).

Conclusion: A high FGFR2 expression could be associated with poor prognostic parameters, while high FGFR3 expression would be associated with good prognostic parameters. These findings might highlight the importance of FGFR-targeted therapy as a FGFR2 antagonist and FGFR3 agonist for the treatment of urothelial carcinoma patients.

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来源期刊
Iranian Journal of Pathology
Iranian Journal of Pathology Medicine-Pathology and Forensic Medicine
CiteScore
2.00
自引率
0.00%
发文量
99
审稿时长
20 weeks
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