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E2F7 可作为肺腺癌的潜在预后生物标志物。

E2F7 serves as a potential prognostic biomarker for lung adenocarcinoma.

机构信息

Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital and Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.

Translational Medicine Collaborative Innovation Center, Shenzhen People's Hospital (The Second Clinical Medical College, Jinan University; The First Affifiliated Hospital, Southern University of Science and Technology), Shenzhen, China.

出版信息

Medicine (Baltimore). 2024 Jan 19;103(3):e34342. doi: 10.1097/MD.0000000000034342.

DOI:10.1097/MD.0000000000034342
PMID:38241554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10798722/
Abstract

E2F transcription factors (E2Fs) are a family of transcription factors critical regulators of the cell cycle, apoptosis, and differentiation, thus influencing tumorigenesis. However, the specific roles of E2Fs in lung adenocarcinoma (LUAD) remain unclear. Data from The Cancer Genome Atlas (TCGA) were used. R version. 4.0.3 and multiple databases (TIMER, cBioportal, gene expression profile interaction analysis [GEPIA], LinkedOmics, and CancerSEA) were utilized to investigate mRNA expression, mutational analysis, prognosis, clinical correlations, co-expressed gene, pathway and network, and single-cell analyses. Immunohistochemistry (IHC) confirmed that E2F transcription factor 7 (E2F7) correlated with LUAD. Among the E2Fs, E2F7 was identified by constructing a prognostic model most significantly associated with overall survival (OS) in LUAD patients. The univariate and multivariate Cox regression analyses showed that E2F7, p-T stage, and p-TNM stage were closely related to OS and progression-free survival (PFS) (P < .05) in LUAD. E2F 7/8 were also identified as significantly associated with tumor stage in the GEPIA database. Compared with paracancerous tissues, E2F7 was up-regulated in LUAD by IHC, and E2F7 might be positively correlated with larger tumors and higher TNM stages. E2F7 may primarily regulate DNA repair, damage, and cell cycle processes and thus affect LUAD tumorigenesis, invasion, and metastasis by LinkedOmics and CancerSEA. E2F7 serves as a potential prognostic biomarker for LUAD.

摘要

E2F 转录因子(E2Fs)是细胞周期、细胞凋亡和分化的关键调节因子家族,因此影响肿瘤发生。然而,E2Fs 在肺腺癌(LUAD)中的具体作用仍不清楚。使用了来自癌症基因组图谱(TCGA)的数据。R 版本 4.0.3 和多个数据库(TIMER、cBioportal、基因表达谱交互分析[GEPIA]、LinkedOmics 和 CancerSEA)用于研究 mRNA 表达、突变分析、预后、临床相关性、共表达基因、途径和网络以及单细胞分析。免疫组织化学(IHC)证实 E2F 转录因子 7(E2F7)与 LUAD 相关。在 E2Fs 中,通过构建与 LUAD 患者总生存(OS)最显著相关的预后模型,确定 E2F7。单因素和多因素 Cox 回归分析显示,E2F7、p-T 期和 p-TNM 期与 OS 和无进展生存(PFS)密切相关(P<0.05)。在 GEPIA 数据库中,E2F7/8 也被确定与肿瘤分期显著相关。与癌旁组织相比,IHC 显示 LUAD 中 E2F7 上调,E2F7 可能与较大的肿瘤和更高的 TNM 分期呈正相关。E2F7 可能主要通过 LinkedOmics 和 CancerSEA 调节 DNA 修复、损伤和细胞周期过程,从而影响 LUAD 的肿瘤发生、侵袭和转移。E2F7 可作为 LUAD 的潜在预后生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb15/10798722/02b3e893e875/medi-103-e34342-g007.jpg
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本文引用的文献

1
Meiotic nuclear divisions 1 (MND1) fuels cell cycle progression by activating a KLF6/E2F1 positive feedback loop in lung adenocarcinoma.有丝分裂核分裂 1 (MND1) 通过激活肺腺癌中的 KLF6/E2F1 正反馈环为细胞周期进程提供燃料。
Cancer Commun (Lond). 2021 Jun;41(6):492-510. doi: 10.1002/cac2.12155. Epub 2021 Mar 18.
2
Circ-AASDH functions as the progression of early stage lung adenocarcinoma by targeting miR-140-3p to activate E2F7 expression.环状AASDH通过靶向miR-140-3p激活E2F7表达,在早期肺腺癌进展中发挥作用。
Transl Lung Cancer Res. 2021 Jan;10(1):57-70. doi: 10.21037/tlcr-20-1062.
3
CDK13 upregulation-induced formation of the positive feedback loop among circCDK13, miR-212-5p/miR-449a and E2F5 contributes to prostate carcinogenesis.
CDK13 上调诱导 circCDK13、miR-212-5p/miR-449a 和 E2F5 之间的正反馈环形成,促进前列腺癌发生。
J Exp Clin Cancer Res. 2021 Jan 4;40(1):2. doi: 10.1186/s13046-020-01814-5.
4
Re: A. Gordon Robertson, Clarice S. Groeneveld, Brian Jordan, et al. Identification of Differential Tumor Subtypes of T1 Bladder Cancer. Eur Urol;2020:533-7.回复:A. 戈登·罗伯逊、克拉丽斯·S. 格罗内维尔德、布莱恩·乔丹等。T1期膀胱癌不同肿瘤亚型的鉴定。《欧洲泌尿外科杂志》;2020年:第533 - 537页。
Eur Urol. 2020 Dec;78(6):e228-e229. doi: 10.1016/j.eururo.2020.09.016. Epub 2020 Sep 28.
5
Is an Estrogen-Responsive LncRNA That Drives Breast Cancer through the E2F1/RB1 Pathway.是一种雌激素反应性长非编码 RNA,通过 E2F1/RB1 通路驱动乳腺癌。
Cancer Res. 2020 Oct 15;80(20):4399-4413. doi: 10.1158/0008-5472.CAN-20-1031. Epub 2020 Aug 21.
6
TIMER2.0 for analysis of tumor-infiltrating immune cells.TIMER2.0 用于分析肿瘤浸润免疫细胞。
Nucleic Acids Res. 2020 Jul 2;48(W1):W509-W514. doi: 10.1093/nar/gkaa407.
7
SNHG7 Contributes to the Progression of Non-Small-Cell Lung Cancer via the SNHG7/miR-181a-5p/E2F7 Axis.SNHG7通过SNHG7/miR-181a-5p/E2F7轴促进非小细胞肺癌的进展。
Cancer Manag Res. 2020 May 7;12:3211-3222. doi: 10.2147/CMAR.S240964. eCollection 2020.
8
Circular RNA ABCB10 promotes non-small cell lung cancer progression by increasing E2F5 expression through sponging miR-584-5p.环状 RNA ABCB10 通过海绵吸附 miR-584-5p 增加 E2F5 表达促进非小细胞肺癌进展。
Cell Cycle. 2020 Jul;19(13):1611-1620. doi: 10.1080/15384101.2020.1761617. Epub 2020 May 18.
9
Downregulation of LINC00665 confers decreased cell proliferation and invasion via the miR-138-5p/E2F3 signaling pathway in NSCLC.下调 LINC00665 通过 miR-138-5p/E2F3 信号通路抑制非小细胞肺癌细胞的增殖和侵袭。
Biomed Pharmacother. 2020 Jul;127:110214. doi: 10.1016/j.biopha.2020.110214. Epub 2020 May 11.
10
Construction of a novel gene-based model for prognosis prediction of clear cell renal cell carcinoma.构建一种用于透明细胞肾细胞癌预后预测的新型基因模型。
Cancer Cell Int. 2020 Jan 28;20:27. doi: 10.1186/s12935-020-1113-6. eCollection 2020.