EZH2和ARID1A表达在尿路上皮癌中的预后意义:免疫组织化学研究。

Pub Date : 2022-03-01 Epub Date: 2021-09-08 DOI:10.1080/01478885.2021.1973309
Reham Sameh, Naglaa Mostafa, Mohamed Ramadan, Samar AbdelRaouf, Khaled Abdelwahab
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引用次数: 0

摘要

尿路上皮癌(UC)中zeste同源物2 (EZH2)和富含at的相互作用结构域1A (ARID1A)表达的增强子尚未得到很好的研究。ARID1A是一种新的肿瘤抑制基因,编码一种在膀胱癌中发生突变的染色质重塑蛋白。zeste同源物2增强子(EZH2)是一种参与基因沉默的转录抑制因子。EZH2扩增已在几种恶性肿瘤中被报道。本研究分析了56例UC患者中EZH2和ARID1A的免疫组化表达,其中包括21例根治性膀胱切除术和35例经尿道肌纤维膀胱肿瘤切除术及辅助膀胱内卡介苗(BCG)免疫治疗。分析两种标志物对肿瘤复发和无复发生存(RFS)的预测作用。75%的病例EZH2标记物高表达,78.6%的病例ARID1A标记物低表达。EZH2高表达和ARID1A低表达与较高的肿瘤分级、分期、存在肌肉侵袭、淋巴结转移、存在合并原位癌(CIS)、较高的复发率和较短的RFS率显著相关。综上所述,EZH2和ARID1A在肿瘤的癌变和分化中发挥作用,可被认为是UC的独立预后因素,并可作为潜在的治疗靶点。
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Prognostic significance of EZH2 and ARID1A expression in urothelial carcinoma: an immunohistochemical study.

Enhancer of zeste homolog 2 (EZH2) and AT-rich interactive domain 1A (ARID1A) expression in urothelial carcinoma (UC) has not been well studied. ARID1A is a novel tumor suppressor gene coding for a chromatin remodeling protein that is mutated in urinary bladder cancer. The enhancer of zeste homolog 2 (EZH2) is a transcriptional repressor involved in gene silencing. Amplification of EZH2 has been reported in several malignancies. This study analyzed the immunohistochemical expression of EZH2 and ARID1A in 56 cases of UC that included (n = 21) cases of radical cystectomy and (n = 35) cases of transurethral resections of bladder tumor (TURBT) with muscle fibers and immunotherapy with adjuvant intravesical bacillus Calmette-Guerin (BCG). The predicting role of both markers for tumor recurrence and recurrence-free survival (RFS) was also analyzed. High EZH2 marker expression was observed in 75% of cases while 78.6% of cases had low ARID1A marker expression. There was a significant negative correlation between the two markers where high EZH2 and low ARID1A expression was significantly associated with higher tumor grade, stage, presence of muscle invasion, lymph node metastasis, presence of concomitant carcinoma in situ (CIS) and higher incidence of recurrence with shorter RFS rate. It was concluded that EZH2 and ARID1A play a role in tumor carcinogenesis and differentiation and could be considered as independent prognostic factors in UC and for use as a potential therapeutic target.

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