Zhang Hua, Sun Wenlong, Qiao Gaofeng, Zhao Bin, Liu Xiangyan, Zhu Feng
Department of Thoracic Surgery, Shandong Provincial Chest Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250013, China.
Department of Thoracic Surgery, Boxing People's Hospital of Shandong Province, Binzhou, Shandong 256500, China.
Gastroenterol Res Pract. 2020 Jul 31;2020:7641761. doi: 10.1155/2020/7641761. eCollection 2020.
Tripartite motif protein 36 (TRIM36) plays a tumor-suppressive role in prostate cancer. However, there is little information on the clinical relevance of TRIM36 expression in esophageal cancer (ESCA).
TRIM36 expression was analyzed by using The Cancer Genome Atlas (TCGA) ESCA dataset as well as by quantitative real-time polymerase chain reaction (PCR) and immunohistochemical (IHC) staining on samples from our hospital.
In the current study, the analysis of TCGA ESCA dataset suggested the decreased expression of TRIM36 in ESCA tissues. Further analyses on samples from our hospital demonstrated that TRIM36 was significantly downregulated in ESCA tissues than in the noncancerous controls at both the mRNA and protein levels. Moreover, gene set enrichment analysis on TCGA ESCA dataset suggested that TRIM36 expression was inversely correlated with the -catenin pathway. IHC staining data showed that 66.25% (53/80) and 51.25% (41/80) of ESCA cases had a low expression of TRIM36 and a high expression of -catenin, respectively. By Fisher's exact test, we found that TRIM36 protein expression was significantly correlated with tumor size ( = 0.0104), tumor stage ( = 0.0169), lymph node metastasis ( = 0.0021), vital status ( = 0.0443), and -catenin expression ( = 0.0329). These findings suggest the potential clinical significance of TRIM36 in ESCA. Kaplan-Meier and log-rank test demonstrated that a low expression of TRIM6 and a high expression of -catenin were associated with poor overall survival of ESCA patients.
Our study provides evidence for the prognostic value of TRIM36 in ESCA.
三联基序蛋白36(TRIM36)在前列腺癌中发挥肿瘤抑制作用。然而,关于TRIM36表达在食管癌(ESCA)中的临床相关性的信息很少。
使用癌症基因组图谱(TCGA)ESCA数据集以及通过定量实时聚合酶链反应(PCR)和免疫组织化学(IHC)染色分析我院样本中的TRIM36表达。
在本研究中,对TCGA ESCA数据集的分析表明TRIM36在ESCA组织中的表达降低。对我院样本的进一步分析表明,TRIM36在ESCA组织中的mRNA和蛋白质水平均显著低于非癌对照。此外,对TCGA ESCA数据集的基因集富集分析表明,TRIM36表达与β-连环蛋白途径呈负相关。IHC染色数据显示,分别有66.25%(53/80)和51.25%(41/80)的ESCA病例TRIM36低表达和β-连环蛋白高表达。通过Fisher精确检验,我们发现TRIM36蛋白表达与肿瘤大小(P = 0.0104)、肿瘤分期(P = 0.0169)、淋巴结转移(P = 0.0021)、生存状态(P = 0.0443)和β-连环蛋白表达(P = 0.0329)显著相关。这些发现提示TRIM36在ESCA中的潜在临床意义。Kaplan-Meier和对数秩检验表明,TRIM6低表达和β-连环蛋白高表达与ESCA患者的总生存期较差有关。
我们的研究为TRIM36在ESCA中的预后价值提供了证据。