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SLC39A1(溶质载体家族 39 成员 1)表达降低预示着早期肝细胞癌患者预后不良。

Decreased SLC39A1 (Solute carrier family 39 member 1) expression predicts unfavorable prognosis in patients with early-stage hepatocellular carcinoma.

机构信息

Department of Gastroenterology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, China.

出版信息

Bioengineered. 2021 Dec;12(1):8147-8156. doi: 10.1080/21655979.2021.1987131.

Abstract

Solute carrier family 39, member 1 (SLC39A1) is a member of the zinc-iron permease family and located to the cell membrane, acting as a zinc uptake transporter. However, the clinical impacts of SLC39A1 in early-stage hepatocellular carcinoma (EHCC) have not been defined. In this research, we compared the differential expression of SLC39A1 in EHCC and normal tissues based on tissue microarray, and the clinical significance of SLC39A1 in EHCC was evaluated as well. Compared with adjacent tissues, SLC39A1 was remarkably decreased in paired EHCC tissues. Besides, decreased SLC39A1 expression was significantly associated with several clinic-pathological features and serum biochemical indicators. Furthermore, Kaplan-Meier analysis exhibited that both overall survival (OS) and relapse-free survival (RFS) of patients with low expression of SLC39A1 were notably poorer than that of patients with high expression. Moreover, Cox regression analyses revealed that low expression of SLC39A1 was an independent prognostic factor for OS in patients with EHCC. Subgroup analysis also revealed beneficiary populations benefiting from the prognostic evaluation using SLC39A1 expression. Collectively, we summarized that downregulated expression of SLC39A1 is a worse prognostic factor for patients with EHCC, which can be used as a promising diagnostic and prognostic biomarker for EHCC.

摘要

溶质载体家族 39,成员 1(SLC39A1)是锌铁渗透酶家族的成员,位于细胞膜上,作为锌摄取转运体。然而,SLC39A1 在早期肝细胞癌(EHCC)中的临床影响尚未确定。在这项研究中,我们基于组织微阵列比较了 SLC39A1 在 EHCC 和正常组织中的差异表达,并评估了 SLC39A1 在 EHCC 中的临床意义。与相邻组织相比,配对的 EHCC 组织中 SLC39A1 的表达明显降低。此外,SLC39A1 表达降低与多种临床病理特征和血清生化指标显著相关。此外,Kaplan-Meier 分析显示,SLC39A1 低表达患者的总生存(OS)和无复发生存(RFS)均明显差于 SLC39A1 高表达患者。此外,Cox 回归分析显示,SLC39A1 低表达是 EHCC 患者 OS 的独立预后因素。亚组分析还显示,SLC39A1 表达可作为 EHCC 患者预后评估的有益人群。综上所述,SLC39A1 的下调表达是 EHCC 患者预后较差的因素,可作为 EHCC 的有前途的诊断和预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3101/8806984/0aa6e6859dbc/KBIE_A_1987131_F0001_OC.jpg

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