The Role of p300 and TMPRSS2 in Prostate Cancer: Immunohistochemical Perspectives and Gleason Correlations.

Cancer diagnosis & prognosis Pub Date : 2025-05-03 eCollection Date: 2025-05-01 DOI:10.21873/cdp.10439
Charitomeni Gioukaki, Alexandros Georgiou, Panagiotis Sarantis, Kostas Palamaris, Andreas C Lazaris, Christos Alamanis, Georgia Eleni Thomopoulou
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Abstract

Background/aim: Transmembrane protease, serine 2 (TMPRSS2), and E1A-associated protein (p300) are important factors in prostate cancer (PCa) pathogenesis, playing significant roles in androgen receptor (AR) signaling and tumor progression. Despite their established role in PCa biology, their immunohistochemical alterations across different Gleason patterns and histological grades remain unclear. This experimental study aimed to assess TMPRSS2 and p300 expression in non-malignant and cancerous prostate tissues, correlating their localization and intensity with Gleason scores and tumor aggressiveness.

Materials and methods: A total of 58 paraffin-embedded prostate adenocarcinoma (PRAD) tissue sections from male patients who underwent radical prostatectomy, including low- and high-grade tumors and high-grade prostatic intraepithelial neoplasia (HGPIN), were analyzed. Immunohistochemistry (IHC) for TMPRSS2 and p300 was performed. Two independent pathologists conducted H-score assessments with complete interobserver concordance, evaluating staining intensity, localization, and expression patterns, correlating findings with Gleason scores and cancer stage.

Results: TMPRSS2 and p300 exhibited variable expression levels across all tissue samples. While TMPRSS2 expression increased in aggressive tumors, its staining intensity did not change significantly across different Gleason grades. p300 over-expression was significantly associated with aggressive tumors, particularly Gleason pattern 5 (p=0.011). High-grade tumors [Gleason ≥7(4+3)] demonstrated higher p300 expression compared to low-grade tumors [Gleason ≤7(3+4)], with minimal staining observed in Gleason score 6.

Conclusion: Expression patterns of TMPRSS2 and p300 correlate with PCa aggressiveness. These findings support the growing evidence suggesting their potential role as prognostic markers and therapeutic targets. The implementation of well-designed studies on a larger scale is of utmost importance, to draw safer conclusions.

p300和TMPRSS2在前列腺癌中的作用:免疫组织化学观点和Gleason相关性。
背景/目的:跨膜蛋白酶、丝氨酸2 (TMPRSS2)和e1a相关蛋白(p300)是前列腺癌(PCa)发病的重要因子,在雄激素受体(AR)信号传导和肿瘤进展中起重要作用。尽管它们在前列腺癌生物学中具有明确的作用,但它们在不同Gleason模式和组织学分级中的免疫组化改变仍不清楚。本实验研究旨在评估TMPRSS2和p300在非恶性和癌性前列腺组织中的表达,以及它们的定位和强度与Gleason评分和肿瘤侵袭性的关系。材料和方法:对行根治性前列腺切除术的男性患者的58例前列腺腺癌(PRAD)石蜡包埋组织切片进行分析,包括低级别肿瘤和高级别前列腺上皮内瘤变(HGPIN)。对TMPRSS2和p300进行免疫组化(IHC)检测。两名独立的病理学家进行了完全一致的h评分评估,评估染色强度、定位和表达模式,将结果与Gleason评分和癌症分期相关联。结果:TMPRSS2和p300在所有组织样本中表现出不同的表达水平。虽然TMPRSS2在侵袭性肿瘤中表达增加,但其染色强度在不同Gleason分级中没有明显变化。p300过表达与侵袭性肿瘤显著相关,尤其是Gleason模式5 (p=0.011)。高级别肿瘤[Gleason≥7(4+3)]与低级别肿瘤[Gleason≤7(3+4)]相比,p300的表达更高,Gleason评分为6时染色最少。结论:TMPRSS2和p300的表达模式与前列腺癌侵袭性相关。这些发现支持了越来越多的证据表明它们作为预后标志物和治疗靶点的潜在作用。为了得出更安全的结论,在更大范围内实施精心设计的研究是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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