Do Anh Toan, Pham Quoc Thang, Nguyen Ngoc Minh Tam, Nguyen Phuc Nguyen, Bui Thi Thanh Tam, Ngo Quoc Dat
Department of Urology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.
Department of Pathology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.
Life (Basel). 2024 Dec 17;14(12):1670. doi: 10.3390/life14121670.
Bladder cancer (BC) presents significant molecular diversity, which affects both prognosis and treatment results. Immunohistochemistry (IHC) facilitates the identification of molecular subtypes and their relationships with clinicopathological features.
We performed an IHC analysis on tissue samples from 107 BC patients, evaluating the expression of markers GATA3, CD44, CK5/6, and CK20. We applied two methods to classify the tumor samples into basal and luminal subtypes. The relationships between these marker expressions, molecular subtypes, clinicopathological characteristics, and TILs were explored.
Most samples showed the expression of GATA3 and CD44, with notable correlations found between CD44 and CK5/6 as well as GATA3 and CK20. CD44 and CD20 expression were linked to a poorer prognosis. Additionally, the luminal and basal subtypes had distinct TIL patterns, which influenced overall survival. A poor prognosis was associated with the basal subtype with low TIL infiltration and the luminal subtype with high TIL infiltration.
Our study clarifies the molecular characteristics of BC, underlining the prognostic importance of CD44 expression and the role of TILs in influencing subtype-specific outcomes. IHC proves valuable in subtype identification and supports personalized treatment strategies.
膀胱癌(BC)呈现出显著的分子多样性,这会影响预后和治疗效果。免疫组织化学(IHC)有助于识别分子亚型及其与临床病理特征的关系。
我们对107例BC患者的组织样本进行了免疫组织化学分析,评估了标志物GATA3、CD44、CK5/6和CK20的表达。我们应用两种方法将肿瘤样本分为基底型和管腔型亚型。探讨了这些标志物表达、分子亚型、临床病理特征和肿瘤浸润淋巴细胞(TILs)之间的关系。
大多数样本显示GATA3和CD44表达,CD44与CK5/6以及GATA3与CK20之间存在显著相关性。CD44和CD20表达与较差的预后相关。此外,管腔型和基底型亚型具有不同的TIL模式,这影响了总生存期。预后不良与TIL浸润低的基底型亚型和TIL浸润高的管腔型亚型相关。
我们的研究阐明了BC的分子特征,强调了CD44表达的预后重要性以及TILs在影响亚型特异性结局中的作用。免疫组织化学在亚型识别中被证明是有价值的,并支持个性化治疗策略。