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生物信息学分析揭示 AKR1B1 在胃癌免疫浸润和临床结局中的重要作用。

Bioinformatics Analysis Reveals the Vital Role of AKR1B1 in Immune Infiltration and Clinical Outcomes of Gastric Cancer.

机构信息

Department of Oncology, Changhai Hospital, Second Military Medical University (Naval Medical University), Shanghai, China.

Department of Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing University, Nanjing, China.

出版信息

DNA Cell Biol. 2023 Jul;42(7):372-389. doi: 10.1089/dna.2022.0644. Epub 2023 Jun 7.

Abstract

Infiltrated immune cells are an important constitute of tumor microenvironment, which exert complex effects on gastric cancer (GC) pathogenesis and progression. By using weighted gene co-expression network analysis, integrating the data from The Cancer Genome Atlas-stomach adenocarcinoma and GSE62254, we identify Aldo-Keto Reductase Family 1 Member B (AKR1B1) as a hub gene for immune regulation in GC. Notably, AKR1B1 is associated with higher immune infiltration and worse histologic grade of GC. In addition, AKR1B1 is an independent factor for predicting the survival rate of GC patients. experiments further demonstrated that AKR1B1-overexpressed THP-1-derived macrophages promoted the proliferation and migration of GC cells. Taken together, AKR1B1 plays an important role in GC progression by regulating immune microenvironment, which could be a biomarker for predicting GC prognosis as well as a potential therapeutic target for GC treatment.

摘要

浸润免疫细胞是肿瘤微环境的重要组成部分,对胃癌(GC)的发病机制和进展有复杂的影响。通过使用加权基因共表达网络分析,整合来自癌症基因组图谱-胃腺癌和 GSE62254 的数据,我们鉴定出醛酮还原酶家族 1 成员 B(AKR1B1)是 GC 中免疫调节的关键基因。值得注意的是,AKR1B1 与 GC 更高的免疫浸润和更差的组织学分级相关。此外,AKR1B1 是预测 GC 患者生存率的独立因素。实验进一步表明,AKR1B1 过表达的 THP-1 衍生的巨噬细胞促进了 GC 细胞的增殖和迁移。综上所述,AKR1B1 通过调节免疫微环境在 GC 进展中发挥重要作用,它可以作为预测 GC 预后的生物标志物,也是 GC 治疗的潜在治疗靶点。

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