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IGF2BP3 过表达预示着膀胱癌预后不良,并与免疫浸润相关。

IGF2BP3 overexpression predicts poor prognosis and correlates with immune infiltration in bladder cancer.

机构信息

Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang, 330000, Jiangxi, China.

Department of Oncology, The First Affiliated Hospital of Nanchang University, Nanchang, 330000, Jiangxi, China.

出版信息

BMC Cancer. 2023 Feb 3;23(1):116. doi: 10.1186/s12885-022-10353-5.

Abstract

BACKGROUND

IGF2BP3 expression is associated with poor prognosis in cancers of multiple tissue origins. However, the precise mechanism of its co-carcinogenic action in bladder cancer is unknown.

METHODS

We aimed to demonstrate the relationship between IGF2BP3 expression and pan-cancer using The Cancer Genome Atlas (TCGA) database. We next validated IGF2BP3 expression in the Gene Expression Omnibus (GEO) database (GSE3167). Receiver operating characteristic (ROC) curve analysis was used to evaluate the diagnostic values of IGF2BP3. Cox and logistic regression were used to explore the factors affecting the prognosis. Protein-protein interactions (PPIs) network was constructed by STRING. Enrichment analyses were performed to infer involved pathways and functional categories of IGF2BP3 using the cluster Profiler package. We applied single-sample gene set enrichment analysis (ssGSEA) algorithm and TIMER database to evaluate the expression level of immune genes.

RESULTS

Pan-cancer analyses reveal that IGF2BP3 was higher in most cancer types, including bladder cancer, and the same results were found in GSE3167. The area under the ROC curve of IGF2BP3 was 0.736, which indicated that IGF2BP3 may be a potential diagnostic biomarker. High IGF2BP3 expression was associated with poorer overall survival (OS) (P = 0.015). For validation, we collected 95 bladder cancer samples and found that IGF2BP3 expression was higher in bladder cancer tissues than that in non-tumor bladder tissues by immunohistochemistry staining. We found a positive correlation between the expression level of IGF2BP3 and the clinical stage of bladder cancer. Immunocyte infiltration analysis showed that high IGF2BP3 expression was correlated with regulating the infiltration level of immune cell, including neutrophil cells and macrophages. IGF2BP3 promotes migration and invasion of bladder cancer cells, while IGF2BP3 inhibition had the opposite effects. Higher IGF2BP3 expression was closely associated with advanced TNM stage.

CONCLUSION

IGF2BP3 overexpression was related to disease progression and poor prognosis, as well as infiltration of immune cells in bladder cancer. IGF2BP3 can be a promising independent prognostic biomarker and potential treatment target for bladder cancer.

摘要

背景

IGF2BP3 的表达与多种组织来源的癌症的不良预后相关。然而,其在膀胱癌中的致癌作用的确切机制尚不清楚。

方法

我们旨在使用癌症基因组图谱(TCGA)数据库证明 IGF2BP3 表达与泛癌之间的关系。接下来,我们在基因表达综合数据库(GEO)数据库(GSE3167)中验证了 IGF2BP3 的表达。使用接收者操作特征(ROC)曲线分析评估 IGF2BP3 的诊断价值。Cox 和逻辑回归用于探索影响预后的因素。通过 STRING 构建蛋白质-蛋白质相互作用(PPI)网络。使用 cluster Profiler 软件包进行富集分析,以推断 IGF2BP3 涉及的途径和功能类别。我们应用单样本基因集富集分析(ssGSEA)算法和 TIMER 数据库来评估免疫基因的表达水平。

结果

泛癌分析显示,IGF2BP3 在大多数癌症类型中均升高,包括膀胱癌,在 GSE3167 中也得到了相同的结果。IGF2BP3 的 ROC 曲线下面积为 0.736,这表明 IGF2BP3 可能是一种潜在的诊断生物标志物。高 IGF2BP3 表达与总生存期(OS)较差相关(P=0.015)。为了验证,我们收集了 95 例膀胱癌样本,通过免疫组织化学染色发现 IGF2BP3 在膀胱癌组织中的表达高于非肿瘤膀胱癌组织。我们发现 IGF2BP3 的表达水平与膀胱癌的临床分期呈正相关。免疫细胞浸润分析表明,高 IGF2BP3 表达与调节免疫细胞浸润水平相关,包括中性粒细胞和巨噬细胞。IGF2BP3 促进膀胱癌细胞的迁移和侵袭,而 IGF2BP3 抑制则有相反的效果。较高的 IGF2BP3 表达与更晚期的 TNM 分期密切相关。

结论

IGF2BP3 的过表达与膀胱癌的疾病进展和不良预后以及免疫细胞浸润有关。IGF2BP3 可以成为膀胱癌有前途的独立预后生物标志物和潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7701/9896754/02cd9aaad24f/12885_2022_10353_Fig1_HTML.jpg

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