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孤立和联合 MCM3 和 Glypican-3 表达在肝细胞癌中的诊断和预后价值:一种新的免疫亚分型预后模型。

Diagnostic and Prognostic Value of Isolated and Combined MCM3 and Glypican-3 Expression in Hepatocellular Carcinoma: A Novel Immunosubtyping Prognostic Model.

机构信息

Department of Basic Medical Sciences, College of Medicine, AlMaarefa University, Riyadh, Saudi Arabia.

Pathology Department, Faculty of Medicine, Mansoura University.

出版信息

Appl Immunohistochem Mol Morphol. 2022;30(10):694-702. doi: 10.1097/PAI.0000000000001080. Epub 2022 Oct 24.

Abstract

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.

摘要

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。

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