Department of Basic Medical Sciences, College of Medicine, AlMaarefa University, Riyadh, Saudi Arabia.
Pathology Department, Faculty of Medicine, Mansoura University.
Appl Immunohistochem Mol Morphol. 2022;30(10):694-702. doi: 10.1097/PAI.0000000000001080. Epub 2022 Oct 24.
Despite diagnostic and therapeutic advances, hepatocellular carcinoma (HCC) remains a leading cause of morbidity/mortality worldwide. This retrospective study investigates the isolated and combined mini-chromosome maintenance complex component 3 (MCM3) and glypican-3 (GPC3) immunohistochemical (IHC) expression in HCC. A novel HCC immunosubtyping model based on combined MCM3/GPC3 expression is introduced and tested in comparison with prognostic variables and survival outcomes. Seventy-six HCC patients who underwent hepatectomy were enrolled. After the collection of clinicopathological, laboratory, and 3-year-survival data, IHC was applied to HCC tissue microarray-prepared sections using anti-MCM3 and GPC3. IHC scoring divided HCCs as: MCM3-high and MCM3-low expression, GPC3-positive and GPC3-negative expression, and combined scoring model immunosubtypes: MCM3-high/GPC3-positive; MCM3-low/GPC3-positive; MCM3-high/GPC3-negative, and MCM3-low/GPC3-negative. Statistical and Kaplan-Meier survival analyses were performed using SPSS version 23. MCM3 was expressed in 84.2% of HCCs. MCM3-high HCCs (60.5%) were significantly associated with lack of tumor capsulation, portal vein thrombosis, high grades, advanced stages, and Child-Pugh Scores B and C (all P≤0.05), and had a tendency for multiplicity, metastasis, solid growth pattern, shorter overall survival (OS) and disease-free survival (DFS). GPC3-positve HCCs (56.6%) were significantly associated with multiplicity and higher alfa-fetoprotein (all P≤0.05) with a tendency for shorter OS and DFS. Among all isolated and combined-expression immunosubtypes, MCM3-high/GPC3-positive HCCs had the worst prognosis and the shortest OS and DFS whereas MCM3-low/GPC3-negative immunosubtype showed the best prognosis and had the longest OS and DFS. MCM3 is defined as diagnostic, prognostic marker, and potential therapeutic target in HCC. The novel MCM3/GPC3 immunosubtyping model provides prognostic indications and stratification criteria for patients with HCC.
尽管在诊断和治疗方面取得了进展,但肝细胞癌(HCC)仍然是全球发病率和死亡率的主要原因。这项回顾性研究调查了孤立和联合微小染色体维持复合物成分 3(MCM3)和磷脂酰聚糖-3(GPC3)免疫组织化学(IHC)在 HCC 中的表达。引入了一种基于联合 MCM3/GPC3 表达的新型 HCC 免疫亚型模型,并与预后变量和生存结果进行了比较。纳入了 76 名接受肝切除术的 HCC 患者。在收集临床病理、实验室和 3 年生存数据后,使用抗 MCM3 和 GPC3 对 HCC 组织微阵列制备的切片进行了 IHC。免疫组化评分将 HCC 分为:MCM3 高表达和 MCM3 低表达、GPC3 阳性和 GPC3 阴性表达,以及联合评分模型免疫亚型:MCM3 高/GPC3 阳性;MCM3 低/GPC3 阳性;MCM3 高/GPC3 阴性和 MCM3 低/GPC3 阴性。使用 SPSS 版本 23 进行统计和 Kaplan-Meier 生存分析。MCM3 在 84.2%的 HCC 中表达。MCM3 高 HCC(60.5%)与缺乏肿瘤包膜、门静脉血栓形成、高分级、晚期、Child-Pugh 评分 B 和 C(均 P≤0.05)显著相关,且具有多发性、转移、实性生长模式、总生存期(OS)和无病生存期(DFS)缩短的趋势。GPC3 阳性 HCC(56.6%)与多发性和较高的甲胎蛋白(均 P≤0.05)显著相关,且 OS 和 DFS 缩短的趋势。在所有孤立和联合表达的免疫亚型中,MCM3 高/GPC3 阳性 HCC 的预后最差,OS 和 DFS 最短,而 MCM3 低/GPC3 阴性免疫亚型的预后最好,OS 和 DFS 最长。MCM3 被定义为 HCC 的诊断、预后标志物和潜在的治疗靶点。新型 MCM3/GPC3 免疫亚型模型为 HCC 患者提供了预后指标和分层标准。