• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

研究癌症中的POU3F4:表达模式、预后意义及在肿瘤免疫中的功能作用。

Investigating POU3F4 in cancer: Expression patterns, prognostic implications, and functional roles in tumor immunity.

作者信息

Chen Weiwei, Ji Yaya, Wang Rui, Ji Ruijie, Lin Yujian, Wu Yuhang, Liu Lehan, Sha Tianle, Li Wen, Zhang Lei, Yang Longfei, Zhang Xinhua, Song Jianxiang

机构信息

Department of Cardiothoracic Surgery, Affiliated Hospital 6 of Nantong University, Yancheng Third People's Hospital, The Yancheng School of Clinical Medicine of Nanjing Medical University, Yancheng, 224002, China.

Department of Radiotherapy, Affiliated Hospital 6 of Nantong University, Yancheng Third People's Hospital, The Yancheng School of Clinical Medicine of Nanjing Medical University, Yancheng, 224002, China.

出版信息

Heliyon. 2024 Dec 31;11(1):e41587. doi: 10.1016/j.heliyon.2024.e41587. eCollection 2025 Jan 15.

DOI:10.1016/j.heliyon.2024.e41587
PMID:39866492
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11760290/
Abstract

Research has demonstrated that POU3F4 is integral to various cancers, in addition to its significance in inner ear development, pancreatic differentiation, as well as neural stem cell differentiation. Nevertheless, comprehensive pan-cancer analyses focusing on POU3F4 remain limited. This study aims to assess the prognostic value of POU3F4 in thirty-three cancers and explore its immune-related functions. Based on data from The Cancer Genome Atlas (TCGA), Cancer Cell Line Encyclopedia (CCLE), Genotype-Tissue Expression (GTE), and Gene Set Cancer Analysis (GSCA), we employed various bioinformatics approaches to investigate the potential carcinogenic effects of POU3F4. Our study encompassed DNA methylation, RNA methylation, tumor mutation burden (TMB), mismatch repair (MMR) genes, microsatellite instability (MSI), the relationship between POU3F4 and prognosis, and immune cell infiltration (ICI) across different tumors. The analysis revealed that POU3F4 expression is typically low in most cancers but is elevated in breast invasive carcinoma, glioblastoma multiforme (GBM), liver hepatocellular carcinoma, and thyroid carcinoma, with the highest levels in GBM. Additionally, POU3F4 expression correlates with cancer prognosis, either positively or negatively. The expression of POU3F4 demonstrated significant associations with MSI in four cancers and TMB in six cancers. POU3F4 expression was significantly linked to DNA methylation in 13 cancer types and RNA methylation in most cancers. It also correlated with the tumor immune microenvironment, immune-related genes, immune checkpoint inhibitors, and drug resistance in various cancers. experiments demonstrated that POU3F4 enhances cell viability, proliferation, and migration in GBM. Our findings indicate that, given its critical role in carcinogenesis and tumor immunity, POU3F4 serves as a prognostic marker in diverse malignancies.

摘要

研究表明,POU3F4除了在内耳发育、胰腺分化以及神经干细胞分化中具有重要意义外,在多种癌症中也不可或缺。然而,针对POU3F4的全面泛癌分析仍然有限。本研究旨在评估POU3F4在33种癌症中的预后价值,并探索其免疫相关功能。基于来自癌症基因组图谱(TCGA)、癌细胞系百科全书(CCLE)、基因型-组织表达(GTE)和基因集癌症分析(GSCA)的数据,我们采用了各种生物信息学方法来研究POU3F4的潜在致癌作用。我们的研究涵盖了DNA甲基化、RNA甲基化、肿瘤突变负担(TMB)、错配修复(MMR)基因、微卫星不稳定性(MSI)、POU3F4与预后的关系以及不同肿瘤中的免疫细胞浸润(ICI)。分析显示,POU3F4在大多数癌症中的表达通常较低,但在乳腺浸润性癌、多形性胶质母细胞瘤(GBM)、肝细胞肝癌和甲状腺癌中升高,在GBM中水平最高。此外,POU3F4的表达与癌症预后呈正相关或负相关。POU3F4的表达在4种癌症中与MSI显著相关,在6种癌症中与TMB显著相关。POU3F4的表达在13种癌症类型中与DNA甲基化显著相关,在大多数癌症中与RNA甲基化显著相关。它还与各种癌症中的肿瘤免疫微环境、免疫相关基因、免疫检查点抑制剂和耐药性相关。实验表明,POU3F4可增强GBM中的细胞活力、增殖和迁移。我们的研究结果表明,鉴于其在致癌作用和肿瘤免疫中的关键作用,POU3F4可作为多种恶性肿瘤的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/0b4174ceb9e1/mmcfigs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/fcef076b90a4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/b3c3dcb07885/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/28518a07a067/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/d2932ed5e250/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/96310e59915a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/86e723134e61/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/6fbad87439d3/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/88da726f8fb3/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/3aa3904b906a/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/fa32e39b3415/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/6bf295dfce4d/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/58ac43006709/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/f63cd95003c0/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/65f9b7070d8e/gr14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/599f40b51b4f/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/0b4174ceb9e1/mmcfigs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/fcef076b90a4/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/b3c3dcb07885/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/28518a07a067/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/d2932ed5e250/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/96310e59915a/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/86e723134e61/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/6fbad87439d3/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/88da726f8fb3/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/3aa3904b906a/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/fa32e39b3415/gr10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/6bf295dfce4d/gr11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/58ac43006709/gr12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/f63cd95003c0/gr13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/65f9b7070d8e/gr14.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/599f40b51b4f/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8365/11760290/0b4174ceb9e1/mmcfigs2.jpg

相似文献

1
Investigating POU3F4 in cancer: Expression patterns, prognostic implications, and functional roles in tumor immunity.研究癌症中的POU3F4:表达模式、预后意义及在肿瘤免疫中的功能作用。
Heliyon. 2024 Dec 31;11(1):e41587. doi: 10.1016/j.heliyon.2024.e41587. eCollection 2025 Jan 15.
2
Ferredoxin 1 is a cuproptosis-key gene responsible for tumor immunity and drug sensitivity: A pan-cancer analysis.铁氧还蛋白1是一种与铜死亡相关的关键基因,负责肿瘤免疫和药物敏感性:一项泛癌分析。
Front Pharmacol. 2022 Sep 21;13:938134. doi: 10.3389/fphar.2022.938134. eCollection 2022.
3
Identification of SHCBP1 as a potential biomarker involving diagnosis, prognosis, and tumor immune microenvironment across multiple cancers.鉴定SHCBP1作为一种潜在的生物标志物,涉及多种癌症的诊断、预后及肿瘤免疫微环境。
Comput Struct Biotechnol J. 2022 Jun 18;20:3106-3119. doi: 10.1016/j.csbj.2022.06.039. eCollection 2022.
4
Pancancer analysis of the correlations of HS6ST2 with prognosis, tumor immunity, and drug resistance.泛癌分析 HS6ST2 与预后、肿瘤免疫和耐药性的相关性。
Sci Rep. 2023 Nov 6;13(1):19209. doi: 10.1038/s41598-023-46525-x.
5
[Pan-cancer analysis of ubiquitin-specific protease 7 and its expression changes in the carcinogenesis of scar ulcer].泛素特异性蛋白酶7的泛癌分析及其在瘢痕溃疡癌变中的表达变化
Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2023 Jun 20;39(6):518-526. doi: 10.3760/cma.j.cn501225-20230421-00137.
6
LncRNA WAC-AS1 expression in human tumors correlates with immune infiltration and affects prognosis.LncRNA WAC-AS1 在人类肿瘤中的表达与免疫浸润相关,并影响预后。
Hereditas. 2023 May 30;160(1):26. doi: 10.1186/s41065-023-00290-z.
7
Systematic Pan-Cancer Analysis Identifies TREM2 as an Immunological and Prognostic Biomarker.系统泛癌症分析鉴定 TREM2 为一种免疫和预后生物标志物。
Front Immunol. 2021 Feb 17;12:646523. doi: 10.3389/fimmu.2021.646523. eCollection 2021.
8
Siglec-9, a Putative Immune Checkpoint Marker for Cancer Progression Across Multiple Cancer Types.唾液酸结合免疫球蛋白样凝集素9(Siglec-9),一种可能与多种癌症进展相关的免疫检查点标志物。
Front Mol Biosci. 2022 Mar 17;9:743515. doi: 10.3389/fmolb.2022.743515. eCollection 2022.
9
Identifies microtubule-binding protein as a novel cancer biomarker associated with ferroptosis and tumor microenvironment.鉴定微管结合蛋白为一种与铁死亡和肿瘤微环境相关的新型癌症生物标志物。
Comput Struct Biotechnol J. 2022 Jun 24;20:3322-3335. doi: 10.1016/j.csbj.2022.06.046. eCollection 2022.
10
Immune Infiltration of MMP14 in Pan Cancer and Its Prognostic Effect on Tumors.基质金属蛋白酶14在泛癌中的免疫浸润及其对肿瘤的预后影响
Front Oncol. 2021 Sep 17;11:717606. doi: 10.3389/fonc.2021.717606. eCollection 2021.

引用本文的文献

1
A systematic review of natural products targeting Nrf2-Keap1-ARE pathway and their influence on neurodegenerative disorders.针对Nrf2-Keap1-ARE通路的天然产物及其对神经退行性疾病影响的系统综述。
Inflammopharmacology. 2025 Sep;33(9):5097-5111. doi: 10.1007/s10787-025-01917-5. Epub 2025 Sep 1.
2
Changes in tumor and cardiac metabolism upon immune checkpoint.免疫检查点作用下肿瘤和心脏代谢的变化
Basic Res Cardiol. 2025 Feb;120(1):133-152. doi: 10.1007/s00395-024-01092-8. Epub 2024 Dec 10.
3
Advances in nephroprotection: the therapeutic role of selenium, silver, and gold nanoparticles in renal health.

本文引用的文献

1
Data-mining-based biomarker evaluation and experimental validation of SHTN1 for bladder cancer.基于数据挖掘的膀胱癌生物标志物SHTN1评估及实验验证
Cancer Genet. 2024 Nov;288-289:43-53. doi: 10.1016/j.cancergen.2024.09.002. Epub 2024 Sep 7.
2
Identification of the novel exhausted T cell CD8 + markers in breast cancer.鉴定乳腺癌中新型耗竭 T 细胞 CD8+标志物。
Sci Rep. 2024 Aug 19;14(1):19142. doi: 10.1038/s41598-024-70184-1.
3
Sangerbox: A comprehensive, interaction-friendly clinical bioinformatics analysis platform.Sangerbox:一个全面的、用户交互友好的临床生物信息学分析平台。
肾保护的进展:硒、银和金纳米颗粒在肾脏健康中的治疗作用
Int Urol Nephrol. 2025 Feb;57(2):479-510. doi: 10.1007/s11255-024-04212-4. Epub 2024 Sep 23.
Imeta. 2022 Jul 8;1(3):e36. doi: 10.1002/imt2.36. eCollection 2022 Sep.
4
Pan-cancer genetic analysis of disulfidptosis-related gene set.泛癌症中二硫键相关基因集的遗传分析。
Cancer Genet. 2023 Nov;278-279:91-103. doi: 10.1016/j.cancergen.2023.10.001. Epub 2023 Oct 10.
5
Targeting MYC-driven lymphoma: lessons learned and future directions.靶向MYC驱动的淋巴瘤:经验教训与未来方向。
Cancer Drug Resist. 2023 Apr 12;6(2):205-222. doi: 10.20517/cdr.2022.127. eCollection 2023.
6
Expression and potential immune involvement of cuproptosis in kidney renal clear cell carcinoma.铜死亡在肾透明细胞癌中的表达及潜在免疫相关性。
Cancer Genet. 2023 Jun;274-275:21-25. doi: 10.1016/j.cancergen.2023.03.002. Epub 2023 Mar 15.
7
Prognostic Values of METTL3 and Its Roles in Tumor Immune Microenvironment in Pan-Cancer.METTL3在泛癌中的预后价值及其在肿瘤免疫微环境中的作用
J Clin Med. 2022 Dec 25;12(1):155. doi: 10.3390/jcm12010155.
8
KEGG for taxonomy-based analysis of pathways and genomes.KEGG 用于基于分类的途径和基因组分析。
Nucleic Acids Res. 2023 Jan 6;51(D1):D587-D592. doi: 10.1093/nar/gkac963.
9
Pan-cancer genetic analysis of cuproptosis and copper metabolism-related gene set.铜死亡及铜代谢相关基因集的泛癌基因分析
Front Oncol. 2022 Oct 6;12:952290. doi: 10.3389/fonc.2022.952290. eCollection 2022.
10
DNA methylation-regulated SNX20 overexpression correlates with poor prognosis, immune cell infiltration, and low-grade glioma progression.DNA 甲基化调控的 SNX20 过表达与不良预后、免疫细胞浸润和低级别胶质瘤进展相关。
Aging (Albany NY). 2022 Jun 27;14(12):5211-5222. doi: 10.18632/aging.204144.