Research Centre for Molecular Pathology, Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Research Centre for Molecular Pathology, Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Pathol Res Pract. 2021 Jan;217:153313. doi: 10.1016/j.prp.2020.153313. Epub 2020 Dec 4.
Mitogen-activated protein kinase kinase 4 (MAP2K4) is a tumor suppressor in many cancers. However, its roles and action mechanisms in pancreatic ductal adenocarcinoma (PDAC) remain unclear. Here, we analyzed MAP2K4 and its downstream kinases (c-Jun N-terminal kinase (JNK) and p38) using immunohistochemical staining and their prognostic significances using univariate and multivariate Cox proportional hazards regression analysis in our PDAC cohort. Then, we validated MAP2K4/JNK/p38 mRNA levels and prognostic significances using The Cancer Genome Atlas (TCGA) database. Finally, we evaluated the effects of MAP2K4 on the proliferation and invasion of PDAC cells. MAP2K4, JNK, and p38 proteins were expressed in 97.3 % (72/74), 95.6 % (65/68), and 88.6 % (62/70) of the samples, respectively, and their levels in tumor tissues were significantly higher than those in normal ducts. MAP2K4 protein expression was lower in male patients (p = 0.028). In our PDAC cohort, advanced TNM stage, low MAP2K4, and high JNK protein levels were significant prognostic factors for poor overall survival (OS) based on a univariate survival analysis (p = 0.006, p < 0.001, and p = 0.004, respectively). N stage and MAP2K4 and JNK protein levels were independent prognostic factors for OS based on multivariate analysis. We then built a prognosis prediction nomogram combining the standard TNM staging system with MAP2K4 and JNK expression that had a Harrell's C-index of 0.645. The new prognosis prediction model effectively stratified the resected patients with PDAC, from both our cohort and TCGA database, into low- and high-risk groups. Finally, MAP2K4 overexpression inhibited pancreatic cancer cell proliferation and migration in vitro. This study shows that reduced protein and mRNA levels of MAP2K4 found in PDAC patients, coupled to in vitro effects observed, support the tumor suppressor role of MAP2K4 in PDAC. Importantly, combining MAP2K4 and JNK expression with the TNM staging system results in a better prediction of postoperative survival of patients with PDAC.
丝裂原活化蛋白激酶激酶 4(MAP2K4)在许多癌症中是一种肿瘤抑制因子。然而,其在胰腺导管腺癌(PDAC)中的作用和作用机制仍不清楚。在这里,我们使用免疫组织化学染色分析了 MAP2K4 及其下游激酶(c-Jun N 末端激酶(JNK)和 p38),并使用单变量和多变量 Cox 比例风险回归分析在我们的 PDAC 队列中分析了其预后意义。然后,我们使用癌症基因组图谱(TCGA)数据库验证了 MAP2K4/JNK/p38 mRNA 水平及其预后意义。最后,我们评估了 MAP2K4 对 PDAC 细胞增殖和侵袭的影响。MAP2K4、JNK 和 p38 蛋白在 74 例样本中的表达率分别为 97.3%(72/74)、95.6%(68/68)和 88.6%(70/70),且肿瘤组织中的表达水平明显高于正常导管组织。男性患者的 MAP2K4 蛋白表达水平较低(p = 0.028)。在我们的 PDAC 队列中,根据单因素生存分析,晚期 TNM 分期、低 MAP2K4 和高 JNK 蛋白水平是总生存期(OS)不良的显著预后因素(p = 0.006、p <0.001 和 p = 0.004)。基于多因素分析,N 期和 MAP2K4 和 JNK 蛋白水平是 OS 的独立预后因素。然后,我们构建了一个结合标准 TNM 分期系统与 MAP2K4 和 JNK 表达的预后预测列线图,其 Harrell's C 指数为 0.645。新的预后预测模型有效地将来自我们的队列和 TCGA 数据库的 PDAC 患者分为低风险和高风险组。最后,MAP2K4 过表达抑制了体外胰腺癌细胞的增殖和迁移。这项研究表明,在 PDAC 患者中发现的 MAP2K4 蛋白和 mRNA 水平降低,以及体外观察到的作用,支持 MAP2K4 在 PDAC 中的肿瘤抑制作用。重要的是,将 MAP2K4 和 JNK 表达与 TNM 分期系统相结合,可更好地预测 PDAC 患者术后的生存情况。