Translational Cancer Medicine Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Department of Pathology and Oral Pathology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Cancer Med. 2019 Nov;8(16):6995-7005. doi: 10.1002/cam4.2576. Epub 2019 Sep 27.
Matrix metalloproteinase 14 (MMP14), a membrane-associated matrix metalloproteinase, has been shown to influence the invasion and metastasis of several solid tumors. Prospero homeobox protein 1 (PROX1), involved in the development and cell fate determination, is also expressed in malignant diseases functioning either as a tumor-suppressing or oncogenic factor. In certain cancers PROX1 appears to transcriptionally suppress MMP14 expression. This study, therefore, aimed to explore the association between MMP14 and PROX1 and understand their potential as prognostic biomarkers in gastric cancer. The cohort consisted of 313 individuals operated for gastric adenocarcinoma between 2000 and 2009 in the Department of Surgery, Helsinki University Hospital. MMP14 and PROX1 expressions were studied using immunohistochemistry in the patient sample and using immunoblotting and immunofluorescence in gastric cancer cell lines. We generated survival curves using the Kaplan-Meier method, determining significance via the log-rank test. A high MMP14 expression associated with being ≥67 years (P = .041), while a positive nuclear PROX1 expression associated with tumors of a diffuse histological type (P = .041) and a high cytoplasmic PROX1 expression (P < .001). Five-year disease-specific survival among patients with a high MMP14 expression was 35.9% (95% confidence interval [CI] 24.9-46.9), compared to 45.3% (95% CI 38.0-52.6) for patients with a low MMP14 (P = .030). Survival was worse specifically among those with a high MMP14 and absent nuclear PROX1 expression (hazard ratio [HR] 1.65; 95% CI 1.09-2.51; P = .019). Thus, this study confirms that a high MMP14 expression predicts a worse survival in gastric cancer, revealing for the first time that survival is particularly worse when PROX1 is low.
基质金属蛋白酶 14(MMP14)是一种膜相关的基质金属蛋白酶,已被证明会影响几种实体瘤的侵袭和转移。Prospero 同源盒蛋白 1(PROX1)参与了发育和细胞命运决定,在恶性疾病中也有表达,它既可以作为肿瘤抑制因子,也可以作为致癌因子。在某些癌症中,PROX1 似乎转录抑制 MMP14 的表达。因此,本研究旨在探讨 MMP14 和 PROX1 之间的关联,并了解它们作为胃癌预后生物标志物的潜力。该队列由 2000 年至 2009 年在赫尔辛基大学医院外科接受胃腺癌手术的 313 名患者组成。在患者样本中使用免疫组织化学研究 MMP14 和 PROX1 的表达,在胃癌细胞系中使用免疫印迹和免疫荧光法。我们使用 Kaplan-Meier 方法生成生存曲线,通过对数秩检验确定显著性。高 MMP14 表达与≥67 岁有关(P=0.041),而核 PROX1 阳性表达与弥漫性组织学类型的肿瘤有关(P=0.041)和高细胞质 PROX1 表达(P<0.001)。高 MMP14 表达患者的 5 年疾病特异性生存率为 35.9%(95%置信区间 [CI] 24.9-46.9),而低 MMP14 表达患者的生存率为 45.3%(95% CI 38.0-52.6)(P=0.030)。特别是在高 MMP14 和核 PROX1 表达缺失的患者中,生存情况更差(风险比 [HR] 1.65;95% CI 1.09-2.51;P=0.019)。因此,本研究证实高 MMP14 表达预测胃癌生存较差,首次揭示当 PROX1 低表达时,生存情况尤其差。