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本文引用的文献

1
Multiple regulatory intrinsically disordered motifs control FOXO4 transcription factor binding and function.多个调节性的无序基序控制 FOXO4 转录因子的结合和功能。
Cell Rep. 2021 Jul 27;36(4):109446. doi: 10.1016/j.celrep.2021.109446.
2
Actein Antagonizes Oral Squamous Cell Carcinoma Proliferation through Activating FoxO1.舞茸拮抗通过激活 FoxO1 抑制口腔鳞状细胞癌增殖。
Pharmacology. 2021;106(9-10):551-563. doi: 10.1159/000515601. Epub 2021 Jun 25.
3
Therapeutic strategies targeting FOXO transcription factors.靶向 FOXO 转录因子的治疗策略。
Nat Rev Drug Discov. 2021 Jan;20(1):21-38. doi: 10.1038/s41573-020-0088-2. Epub 2020 Nov 10.
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The role of ubiquitination and deubiquitination in cancer metabolism.泛素化和去泛素化在癌症代谢中的作用。
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Pitavastatin induces apoptosis in oral squamous cell carcinoma through activation of FOXO3a.培伐他汀通过激活 FOXO3a 诱导口腔鳞状细胞癌凋亡。
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FOXO transcription factor family in cancer and metastasis.叉头框转录因子家族与癌症和转移。
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7
Investigating the role and mechanism of microRNA-196a in oral squamous cell carcinoma by targeting FOXO1.通过靶向FOXO1研究微小RNA-196a在口腔鳞状细胞癌中的作用及机制。
Exp Ther Med. 2020 Jun;19(6):3707-3715. doi: 10.3892/etm.2020.8614. Epub 2020 Mar 19.
8
Exosome mediated miR-155 delivery confers cisplatin chemoresistance in oral cancer cells via epithelial-mesenchymal transition.外泌体介导的miR-155传递通过上皮-间质转化赋予口腔癌细胞顺铂化疗耐药性。
Oncotarget. 2020 Mar 31;11(13):1157-1171. doi: 10.18632/oncotarget.27531.
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MicroRNA Involvement in Signaling Pathways During Viral Infection.病毒感染期间微小RNA参与信号通路
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A Review of 1-Regulated Metabolic Diseases and Related Drug Discoveries.1-调节代谢疾病的综述及相关药物发现。
Cells. 2020 Jan 10;9(1):184. doi: 10.3390/cells9010184.

FOXO1:口腔鳞状细胞癌中的关键先驱因子。

FOXO1: a pivotal pioneer factor in oral squamous cell carcinoma.

作者信息

Remadevi Viji, Muraleedharan Parvathy, Sreeja Sreeharshan

机构信息

Cancer Research Program, Rajiv Gandhi Centre for Biotechnology Thiruvananthapuram, Kerala 695014, India.

Department of Botany, Mount Carmel College Autonomous Bengaluru, Karnataka 560001, India.

出版信息

Am J Cancer Res. 2021 Oct 15;11(10):4700-4710. eCollection 2021.

PMID:34765288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8569351/
Abstract

The transcription factor FOXO1 regulates cell cycle progression, apoptosis and oxidative stress. Interestingly, numerous studies have implicated their positive role in tumor suppression, angiogenesis and metastasis in oral squamous cell carcinoma (OSCC). Distinct post-transcriptional and post-translational modifications actuate the physiological role of FOXO1 in OSCC. Here, we evaluate the role of FOXO1 proteins in OSCC, their fundamental structure and the major players involved in FOXO1 regulation and how they are Pharmacologically modulated in OSCC. Finally, their role in regulating epithelial-mesenchymal transition (EMT), autophagy, stress tolerance and stemness, which would significantly aid in novel potential oversight for future research and thus developing strategies to prevent or reverse OSCC.

摘要

转录因子FOXO1调节细胞周期进程、细胞凋亡和氧化应激。有趣的是,大量研究表明其在口腔鳞状细胞癌(OSCC)的肿瘤抑制、血管生成和转移中发挥积极作用。不同的转录后和翻译后修饰激活了FOXO1在OSCC中的生理作用。在此,我们评估FOXO1蛋白在OSCC中的作用、其基本结构以及参与FOXO1调节的主要因子,以及它们在OSCC中是如何受到药理学调节的。最后,评估它们在调节上皮-间质转化(EMT)、自噬、应激耐受性和干性方面的作用,这将极大地有助于未来研究的新潜在监督,并从而制定预防或逆转OSCC的策略。