Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.
Medical Laboratory Department, Faculty of Applied Medical Sciences, King Abdulaziz University, Saudi Arabia.
Libyan J Med. 2021 Dec;16(1):1994741. doi: 10.1080/19932820.2021.1994741.
The extracellular matrix (ECM) disruption and cytoskeleton reorganization are crucial events in tumor proliferation and invasion. E-Cadherin (E-CAD) is a member of cell adhesion molecules involved in cell-cell junctions and ECM stability. The loss of E-CAD expression is associated with cancer progression and metastasis. This retrospective study aimed to assess E-CAD protein expression in ovarian cancer (OC) tissues and to evaluate its prognostic value.
143 formalin-fixed and paraffin-embedded (FFPE) blocks of primary advanced stages OC were retrieved and used to construct Tissue microarrays. Automated immunohistochemistry technique was performed to evaluate E-CAD protein expression patterns in OC.
E-CAD protein expression was significantly correlated with OC histological subtype (p < 0.0001), while borderline significant correlations were observed with both tumor grade (p = 0.06) and stage (p = 0.07). Interestingly, Kaplan-Meier survival analysis showed that OC patients with membranous E-CAD expression survived longer than those with no E-CAD expression mainly those at advanced stages (p < 0.009). Further in silico analysis confirms the key roles of E-CAD in OC molecular functions.
we reported a prognosis value of membranous E-CAD in advanced stage OC patients. Further validation using larger cohorts is recommended to extract clinically relevant outcomes towards better OC management and individualized oncology.
细胞外基质(ECM)的破坏和细胞骨架的重组是肿瘤增殖和侵袭的关键事件。E-钙黏蛋白(E-CAD)是细胞黏附分子的成员,参与细胞-细胞连接和 ECM 的稳定性。E-CAD 表达的丧失与癌症的进展和转移有关。本回顾性研究旨在评估卵巢癌(OC)组织中 E-CAD 蛋白的表达,并评估其预后价值。
从 143 例福尔马林固定和石蜡包埋(FFPE)的原发性晚期 OC 组织块中检索并用于构建组织微阵列。采用自动化免疫组织化学技术评估 OC 中 E-CAD 蛋白的表达模式。
E-CAD 蛋白表达与 OC 的组织学亚型显著相关(p<0.0001),与肿瘤分级(p=0.06)和分期(p=0.07)也有显著的相关性。有趣的是,Kaplan-Meier 生存分析显示,具有膜性 E-CAD 表达的 OC 患者比没有 E-CAD 表达的患者存活时间更长,主要是在晚期患者中(p<0.009)。进一步的计算分析证实了 E-CAD 在 OC 分子功能中的关键作用。
我们报告了膜性 E-CAD 在晚期 OC 患者中的预后价值。建议使用更大的队列进行进一步验证,以提取对 OC 管理和个体化肿瘤学有临床意义的结果。