Department of Oncology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China.
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China.
Int J Oncol. 2020 Jul;57(1):122-138. doi: 10.3892/ijo.2020.5048. Epub 2020 Apr 15.
SAC3 domain containing 1 (SAC3D1) has been reported to be involved in numerous types of cancer. However, the role of SAC3D1 in GC has not yet been elucidated. In the present study, the mRNA expression level of SAC3D1 between GC and normal tissues were assessed with a continuous variable meta‑analysis based on multiple datasets from public databases. The protein expression level of SAC3D1 in GC and normal tissues was assessed by an in‑house immunohistochemistry (IHC). The association between SAC3D1 expression and some clinical parameters was assessed based on the TCGA and IHC data. Survival analysis was performed to assess the association between SAC3D1 expression and the survival of GC patients. The co‑expressed genes of SAC3D1 were determined by integrating three online tools, and the enrichment analyses were performed to determine SAC3D1‑related pathways and hub co‑expressed genes. SAC3D1 was significantly upregulated in GC tumor tissues in comparison to normal tissues with the SMD being 0.45 (0.12, 0.79). The IHC results also indicated that SAC3D1 protein expression in GC tissues was markedly higher than in normal tissues. The SMD following the addition of the IHC data was 0.59 (0.11, 1.07). The protein levels of SAC3D1 were positively associated with the histological grade, T stage and N stage of GC (P<0.001). The TCGA data also revealed that the SAC3D1 mRNA level was significantly associated with the N stage (P<0.001). Moreover, prognosis analysis indicated that SAC3D1 was closely associated with the prognosis of patients with GC. Moreover, 410 co‑expressed genes of SAC3D1 were determined, and these genes were mainly enriched in the cell cycle. In total, 4 genes (CDK1, CCNB1, CCNB2 and CDC20) were considered key co‑expressed genes. On the whole, these findings demonstrate that SAC3D1 is highly expressed in GC and may be associated with the progression of GC.
SAC3 结构域包含 1 个(SAC3D1)已被报道参与多种类型的癌症。然而,SAC3D1 在 GC 中的作用尚未阐明。在本研究中,基于来自公共数据库的多个数据集,采用连续变量荟萃分析评估了 GC 和正常组织中 SAC3D1 的 mRNA 表达水平。采用内部免疫组织化学(IHC)评估了 GC 和正常组织中 SAC3D1 的蛋白表达水平。根据 TCGA 和 IHC 数据评估了 SAC3D1 表达与某些临床参数之间的关系。生存分析用于评估 SAC3D1 表达与 GC 患者生存之间的关系。通过整合三个在线工具确定了 SAC3D1 的共表达基因,并进行了富集分析以确定 SAC3D1 相关通路和枢纽共表达基因。与正常组织相比,GC 肿瘤组织中 SAC3D1 显著上调,SMD 为 0.45(0.12,0.79)。IHC 结果还表明,GC 组织中 SAC3D1 蛋白表达明显高于正常组织。加入 IHC 数据后的 SMD 为 0.59(0.11,1.07)。SAC3D1 蛋白水平与 GC 的组织学分级、T 分期和 N 分期呈正相关(P<0.001)。TCGA 数据还显示,SAC3D1 mRNA 水平与 N 分期显著相关(P<0.001)。此外,预后分析表明 SAC3D1 与 GC 患者的预后密切相关。此外,确定了 410 个 SAC3D1 的共表达基因,这些基因主要富集在细胞周期中。共有 4 个基因(CDK1、CCNB1、CCNB2 和 CDC20)被认为是关键共表达基因。总的来说,这些发现表明 SAC3D1 在 GC 中高度表达,可能与 GC 的进展有关。