Department of Pediatrics, Affiliated Hospital of Jiangnan University, Wuxi, 214122, Jiangsu, China.
Laboratory of Genomic and Precision Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, Jiangsu, China.
BMC Med Genomics. 2023 Mar 27;16(1):61. doi: 10.1186/s12920-023-01489-9.
Solute Carrier Family 31 Member 1 (SLC31A1) has recently been identified as a cuproptosis-regulatory gene. Recent studies have indicated that SLC31A1 may play a role in colorectal and lung cancer tumorigenesis. However, the role of SLC31A1 and its cuproptosis-regulatory functions in multiple tumor types remains to be further elucidated.
Online websites and datasets such as HPA, TIMER2, GEPIA, OncoVar, and cProSite were used to extract data on SLC31A1 in multiple cancers. DAVID and BioGRID were used to conduct functional analysis and construct the protein-protein interaction (PPI) network, respectively. The protein expression data of SLC31A1 was obtained from the cProSite database.
The Cancer Genome Atlas (TCGA) datasets showed increased SLC31A1 expression in tumor tissues compared with non-tumor tissues in most tumor types. In patients with tumor types including adrenocortical carcinoma, low-grade glioma, or mesothelioma, higher SLC31A1 expression was associated with shorter overall survival and disease-free survival. S105Y was the most prevalent point mutation in SLC31A1 in TCGA pan-cancer datasets. Moreover, SLC31A1 expression was positively correlated with the infiltration of immune cells such as macrophages and neutrophils in tumor tissues in several tumor types. Functional enrichment analysis showed that SLC31A1 co-expressed genes were involved in protein binding, integral components of the membrane, metabolic pathways, protein processing, and endoplasmic reticulum. Copper Chaperone For Superoxide Dismutase, Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunit Alpha and Solute Carrier Family 31 Member 2 were copper homeostasis-regulated genes shown in the PPI network, and their expression was positively correlated with SLC31A1. Analysis showed there was a correlation between SLC31A1 protein and mRNA in various tumors.
These findings demonstrated that SLC31A1 is associated with multiple tumor types and disease prognosis. SLC31A1 may be a potential key biomarker and therapeutic target in cancers.
溶质载体家族 31 成员 1(SLC31A1)最近被确定为铜死亡调控基因。最近的研究表明,SLC31A1 可能在结直肠癌和肺癌的肿瘤发生中发挥作用。然而,SLC31A1 在多种肿瘤类型中的作用及其铜死亡调控功能仍有待进一步阐明。
使用 HPA、TIMER2、GEPIA、OncoVar 和 cProSite 等在线网站和数据集提取多种癌症中 SLC31A1 的数据。使用 DAVID 和 BioGRID 分别进行功能分析和构建蛋白质-蛋白质相互作用(PPI)网络。从 cProSite 数据库获取 SLC31A1 的蛋白质表达数据。
癌症基因组图谱(TCGA)数据集显示,大多数肿瘤类型中肿瘤组织的 SLC31A1 表达高于非肿瘤组织。在肾上腺皮质癌、低级别胶质瘤或间皮瘤等肿瘤类型的患者中,SLC31A1 表达较高与总生存期和无病生存期较短相关。在 TCGA 泛癌数据集中,SLC31A1 最常见的点突变是 S105Y。此外,SLC31A1 表达与几种肿瘤类型肿瘤组织中巨噬细胞和中性粒细胞等免疫细胞的浸润呈正相关。功能富集分析表明,SLC31A1 共表达基因参与蛋白质结合、膜的完整成分、代谢途径、蛋白质加工和内质网。PPI 网络中显示铜伴侣超氧化物歧化酶、磷脂酰肌醇-4,5-二磷酸 3-激酶催化亚单位α和溶质载体家族 31 成员 2 是铜稳态调节基因,它们的表达与 SLC31A1 呈正相关。分析表明,在各种肿瘤中,SLC31A1 蛋白与 mRNA 之间存在相关性。
这些发现表明 SLC31A1 与多种肿瘤类型和疾病预后相关。SLC31A1 可能是癌症中潜在的关键生物标志物和治疗靶标。