Li Bingyu, Huang Larry, Huang Jialing, Li Jianhong
Department of Pathology, Icahn School of Medicine at Mount Sinai-Morningside/West, New York City, NY 10019, USA.
College of Arts and Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA.
Diagnostics (Basel). 2025 Aug 25;15(17):2144. doi: 10.3390/diagnostics15172144.
Hepatocellular carcinoma (HCC) remains a global health challenge due to molecular heterogeneity and frequent delayed diagnosis. This comprehensive review synthesizes recent immunohistochemistry (IHC) advancements for HCC diagnosis, prognostication, and therapeutic prediction. We systematically evaluate conventional markers, such as hepatocyte paraffin 1 (HepPar1), arginase-1 (Arg-1), and glypican-3 (GPC3), as well as emerging biomarkers, detailing their diagnostic sensitivities and specificities in HCC with varied tumor differentiation. Prognostic immunostaining markers, such as Ki-67 proliferation index and vascular endothelial growth factor (VEGF) overexpression, correlate with reduced 5-year survival, while novel immune checkpoint IHC markers (PD-L1 and CTLA-4) predict response to immunotherapy, particularly in advanced HCC. This work provides evidence-based recommendations for optimizing IHC utilization in clinical practice while identifying knowledge gaps in biomarker validation and standardization.
由于分子异质性和频繁的诊断延迟,肝细胞癌(HCC)仍然是一项全球性的健康挑战。这篇综述综合了肝细胞癌诊断、预后评估及治疗预测方面免疫组化(IHC)的最新进展。我们系统评估了传统标志物,如肝细胞石蜡1(HepPar1)、精氨酸酶-1(Arg-1)和磷脂酰肌醇蛋白聚糖-3(GPC3),以及新兴生物标志物,详细阐述了它们在不同肿瘤分化程度的肝细胞癌中的诊断敏感性和特异性。预后免疫染色标志物,如Ki-67增殖指数和血管内皮生长因子(VEGF)过表达,与5年生存率降低相关,而新型免疫检查点免疫组化标志物(PD-L1和CTLA-4)可预测免疫治疗反应,尤其是在晚期肝细胞癌中。这项工作为在临床实践中优化免疫组化的应用提供了循证建议,同时也指出了生物标志物验证和标准化方面的知识空白。