• 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

早期生长反应家族成员 1-4 在肝细胞癌中的研究现状:它们的生物学作用和诊断价值。

The Landscape of Early Growth Response Family Members 1-4 in Hepatocellular Carcinoma: Their Biological Roles and Diagnostic Utility.

机构信息

Department of General Surgery, Xiamen Fifth Hospital, Xiamen, China.

Medical Department, Xiamen Fifth Hospital, Xiamen, China.

出版信息

Dis Markers. 2022 Aug 22;2022:3144742. doi: 10.1155/2022/3144742. eCollection 2022.

DOI:10.1155/2022/3144742
PMID:36046377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9424002/
Abstract

The incidence of hepatocellular carcinoma (HCC), which is one of the most frequent types of cancer seen all over the world, is steadily growing from year to year. EGR genes are members of the early growth response (EGR) gene family. It has been shown that EGR genes play an increasingly essential role in the development of tumors and the progression of numerous malignancies. However, the possible diagnostic and prognostic roles of EGR genes in HCC have only been examined in a limited number of studies. Expression and methylation data on EGR family members were obtained from TCGA datasets. The prognostic values of EGR members were studied. Additionally, the correlations of EGR members with immune cells were assessed through the single-sample gene set enrichment analysis (ssGSEA). In this study, we found that the expression of EGR1, EGR2, EGR3, and EGR4 was distinctly decreased in HCC specimens compared with nontumor specimens. ROC assays confirmed that they have a strong ability in screening HCC specimens from nontumor specimens. According to the findings of Pearson's correlation, EGR1, EGR2, EGR3, and EGR4 were found to have a negative association with the methylation level. Survival study revealed that EGR1, EGR2, and EGR3 were associated with the clinical outcome of HCC patients. Immune cell enrichment analysis demonstrated that the expressions of all EGR members were positively related to the levels of most types of immune cells, such as macrophages, NK cells, B cells, T cells, eosinophils, and CD8 T cells. Overall, the current work demonstrated the expression mode and prognostic value of EGR members in HCC in a comprehensive manner, offering insights for further research of the EGR family as possible clinical biomarkers in HCC.

摘要

肝细胞癌(HCC)是世界上最常见的癌症类型之一,其发病率逐年稳步上升。EGR 基因是早期生长反应(EGR)基因家族的成员。已经表明,EGR 基因在肿瘤的发展和许多恶性肿瘤的进展中起着越来越重要的作用。然而,EGR 基因在 HCC 中的可能诊断和预后作用仅在少数研究中进行了检查。从 TCGA 数据集获得 EGR 家族成员的表达和甲基化数据。研究了 EGR 成员的预后价值。此外,通过单样本基因集富集分析(ssGSEA)评估了 EGR 成员与免疫细胞的相关性。在这项研究中,我们发现 EGR1、EGR2、EGR3 和 EGR4 的表达在 HCC 标本中明显低于非肿瘤标本。ROC 检测证实它们具有从非肿瘤标本中筛选 HCC 标本的强大能力。根据 Pearson 相关性的研究结果,发现 EGR1、EGR2、EGR3 和 EGR4 与甲基化水平呈负相关。生存研究表明 EGR1、EGR2 和 EGR3 与 HCC 患者的临床结局相关。免疫细胞富集分析表明,所有 EGR 成员的表达与大多数类型的免疫细胞(如巨噬细胞、NK 细胞、B 细胞、T 细胞、嗜酸性粒细胞和 CD8 T 细胞)的水平呈正相关。总体而言,本研究全面展示了 EGR 成员在 HCC 中的表达模式和预后价值,为进一步研究 EGR 家族作为 HCC 可能的临床生物标志物提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/230e3331d38d/DM2022-3144742.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/1a7d11c08f1f/DM2022-3144742.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/ce99055d7bed/DM2022-3144742.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/8eede0af7f3c/DM2022-3144742.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/f014d3592ab4/DM2022-3144742.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/230e3331d38d/DM2022-3144742.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/1a7d11c08f1f/DM2022-3144742.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/ce99055d7bed/DM2022-3144742.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/8eede0af7f3c/DM2022-3144742.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/f014d3592ab4/DM2022-3144742.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dac9/9424002/230e3331d38d/DM2022-3144742.005.jpg

相似文献

1
The Landscape of Early Growth Response Family Members 1-4 in Hepatocellular Carcinoma: Their Biological Roles and Diagnostic Utility.早期生长反应家族成员 1-4 在肝细胞癌中的研究现状:它们的生物学作用和诊断价值。
Dis Markers. 2022 Aug 22;2022:3144742. doi: 10.1155/2022/3144742. eCollection 2022.
2
An integrated pan-cancer analysis of identifying biomarkers about the EGR family genes in human carcinomas.基于 EGR 家族基因在人类癌症中鉴定生物标志物的综合泛癌分析。
Comput Biol Med. 2022 Sep;148:105889. doi: 10.1016/j.compbiomed.2022.105889. Epub 2022 Jul 30.
3
EGR1, EGR2, and EGR3 activate the expression of their coregulator NAB2 establishing a negative feedback loop in cells of neuroectodermal and epithelial origin.EGR1、EGR2 和 EGR3 激活其共调节剂 NAB2 的表达,在神经外胚层和上皮细胞中建立负反馈回路。
J Cell Biochem. 2010 Sep 1;111(1):207-17. doi: 10.1002/jcb.22690.
4
Redundant role for early growth response transcriptional regulators in thymocyte differentiation and survival.早期生长反应转录调节因子在胸腺细胞分化和存活中的多余作用。
J Immunol. 2007 Jun 1;178(11):6796-805. doi: 10.4049/jimmunol.178.11.6796.
5
Early growth response transcriptional regulators are dispensable for macrophage differentiation.早期生长反应转录调节因子对于巨噬细胞分化并非必需。
J Immunol. 2007 Mar 1;178(5):3038-47. doi: 10.4049/jimmunol.178.5.3038.
6
Modulation of early growth response (EGR) transcription factor-dependent gene expression by using recombinant adenovirus.利用重组腺病毒调节早期生长反应(EGR)转录因子依赖性基因表达。
Gene. 2000 Nov 27;258(1-2):63-9. doi: 10.1016/s0378-1119(00)00445-5.
7
Early growth response genes 2 and 3 induced by AP-1 and NF-κB modulate TGF-β1 transcription in NK1.1 CD4 NKG2D T cells.早期生长反应基因 2 和 3 通过 AP-1 和 NF-κB 诱导,调节 NK1.1 CD4 NKG2D T 细胞中的 TGF-β1 转录。
Cell Signal. 2020 Dec;76:109800. doi: 10.1016/j.cellsig.2020.109800. Epub 2020 Oct 1.
8
Comprehensive Landscape of ARID Family Members and Their Association with Prognosis and Tumor Microenvironment in Hepatocellular Carcinoma.ARID 家族成员的全面分析及其与肝细胞癌预后和肿瘤微环境的关系。
J Immunol Res. 2022 Mar 30;2022:1688460. doi: 10.1155/2022/1688460. eCollection 2022.
9
Study on the Prognostic Values of TTC36 Correlated with Immune Infiltrates and Its Methylation in Hepatocellular Carcinoma.探讨 TTC36 与肝癌免疫浸润及其甲基化相关的预后价值。
J Immunol Res. 2022 Jul 8;2022:7267131. doi: 10.1155/2022/7267131. eCollection 2022.
10
Transcription factor EGR-1 inhibits growth of hepatocellular carcinoma and esophageal carcinoma cell lines.转录因子EGR-1抑制肝癌和食管癌细胞系的生长。
World J Gastroenterol. 2002 Apr;8(2):203-7. doi: 10.3748/wjg.v8.i2.203.

引用本文的文献

1
EGR1 inhibits clear cell renal cell carcinoma proliferation and metastasis via the MAPK15 pathway.EGR1通过MAPK15途径抑制肾透明细胞癌的增殖和转移。
Oncol Res. 2025 Jan 16;33(2):347-356. doi: 10.32604/or.2024.056039. eCollection 2025.
2
To identify biomarkers associated with the transfer of diabetes combined with cancer in human genes using bioinformatics analysis.利用生物信息学分析鉴定与人类基因中糖尿病合并癌症转移相关的生物标志物。
Medicine (Baltimore). 2023 Sep 15;102(37):e35080. doi: 10.1097/MD.0000000000035080.

本文引用的文献

1
Roles of small extracellular vesicles in the development, diagnosis and possible treatment strategies for hepatocellular carcinoma (Review).小细胞外囊泡在肝细胞癌的发展、诊断及可能的治疗策略中的作用(综述)。
Int J Oncol. 2022 Aug;61(2). doi: 10.3892/ijo.2022.5381. Epub 2022 Jun 8.
2
Tumour-infiltrating B cells: immunological mechanisms, clinical impact and therapeutic opportunities.肿瘤浸润 B 细胞:免疫机制、临床影响和治疗机会。
Nat Rev Cancer. 2022 Jul;22(7):414-430. doi: 10.1038/s41568-022-00466-1. Epub 2022 Apr 7.
3
Targeting cancer metabolism in the era of precision oncology.
精准肿瘤学时代的肿瘤代谢靶向治疗。
Nat Rev Drug Discov. 2022 Feb;21(2):141-162. doi: 10.1038/s41573-021-00339-6. Epub 2021 Dec 3.
4
Diagnosis and prognosis models for hepatocellular carcinoma patient's management based on tumor mutation burden.基于肿瘤突变负荷的肝细胞癌患者管理的诊断和预后模型。
J Adv Res. 2021 Feb 9;33:153-165. doi: 10.1016/j.jare.2021.01.018. eCollection 2021 Nov.
5
Prognostic role of EGR1 in breast cancer: a systematic review.EGR1 在乳腺癌中的预后作用:系统评价。
BMB Rep. 2021 Oct;54(10):497-504. doi: 10.5483/BMBRep.2021.54.10.087.
6
EGR2-mediated regulation of mA reader IGF2BP proteins drive RCC tumorigenesis and metastasis via enhancing S1PR3 mRNA stabilization.EGR2介导的mA阅读器IGF2BP蛋白调控通过增强S1PR3 mRNA稳定性驱动肾细胞癌的肿瘤发生和转移。
Cell Death Dis. 2021 Jul 29;12(8):750. doi: 10.1038/s41419-021-04038-3.
7
EGR3-HDAC6-IL-27 Axis Mediates Allergic Inflammation and Is Necessary for Tumorigenic Potential of Cancer Cells Enhanced by Allergic Inflammation-Promoted Cellular Interactions.EGR3-HDAC6-IL-27 轴介导过敏炎症,并对过敏炎症促进的细胞相互作用增强的癌细胞的致瘤潜能是必需的。
Front Immunol. 2021 Jun 21;12:680441. doi: 10.3389/fimmu.2021.680441. eCollection 2021.
8
EGR1/2 Inhibits Papillary Thyroid Carcinoma Cell Growth by Suppressing the Expression of PTEN and BAX.EGR1/2通过抑制PTEN和BAX的表达来抑制甲状腺乳头状癌细胞的生长。
Biochem Genet. 2021 Dec;59(6):1544-1557. doi: 10.1007/s10528-021-10075-6. Epub 2021 May 10.
9
The Role of the Transcription Factor EGR1 in Cancer.转录因子EGR1在癌症中的作用。
Front Oncol. 2021 Mar 24;11:642547. doi: 10.3389/fonc.2021.642547. eCollection 2021.
10
CD8 T Cell Responses during HCV Infection and HCC.丙型肝炎病毒感染和肝癌过程中的CD8 T细胞反应
J Clin Med. 2021 Mar 2;10(5):991. doi: 10.3390/jcm10050991.