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本文引用的文献

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Expressed HNSCC variants by HPV-status in a well-characterized Michigan cohort.在一个特征明确的密歇根队列中,按 HPV 状态表达的 HNSCC 变体。
Sci Rep. 2018 Jul 30;8(1):11458. doi: 10.1038/s41598-018-29599-w.
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Oxidative Phosphorylation as an Emerging Target in Cancer Therapy.氧化磷酸化作为癌症治疗的新兴靶点。
Clin Cancer Res. 2018 Jun 1;24(11):2482-2490. doi: 10.1158/1078-0432.CCR-17-3070. Epub 2018 Feb 2.
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The Human Papillomavirus E6 Oncoprotein Targets USP15 and TRIM25 To Suppress RIG-I-Mediated Innate Immune Signaling.人乳头瘤病毒E6癌蛋白靶向USP15和TRIM25以抑制RIG-I介导的天然免疫信号传导。
J Virol. 2018 Feb 26;92(6). doi: 10.1128/JVI.01737-17. Print 2018 Mar 15.
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HPV Integration in HNSCC Correlates with Survival Outcomes, Immune Response Signatures, and Candidate Drivers.HPV 整合与头颈部鳞状细胞癌的生存结局、免疫反应特征和候选驱动因素相关。
Mol Cancer Res. 2018 Jan;16(1):90-102. doi: 10.1158/1541-7786.MCR-17-0153. Epub 2017 Sep 19.
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Subtypes of HPV-Positive Head and Neck Cancers Are Associated with HPV Characteristics, Copy Number Alterations, PIK3CA Mutation, and Pathway Signatures.人乳头瘤病毒(HPV)阳性头颈癌的亚型与HPV特征、拷贝数改变、PIK3CA突变及通路特征相关。
Clin Cancer Res. 2016 Sep 15;22(18):4735-45. doi: 10.1158/1078-0432.CCR-16-0323. Epub 2016 Apr 18.
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Detecting Differentially Expressed Genes with RNA-seq Data Using Backward Selection to Account for the Effects of Relevant Covariates.利用反向选择检测RNA测序数据中的差异表达基因以考虑相关协变量的影响
J Agric Biol Environ Stat. 2015;20(4):577-597. doi: 10.1007/s13253-015-0226-1. Epub 2015 Oct 1.
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RNA-Enrich: a cut-off free functional enrichment testing method for RNA-seq with improved detection power.RNA-Enrich:一种用于RNA测序的无阈值功能富集测试方法,具有更高的检测能力。
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E6 viral protein ratio correlates with outcomes in human papillomavirus related oropharyngeal cancer.E6病毒蛋白比率与人类乳头瘤病毒相关口咽癌的预后相关。
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10
Regulation of the Wnt/β-Catenin Signaling Pathway by Human Papillomavirus E6 and E7 Oncoproteins.人乳头瘤病毒E6和E7癌蛋白对Wnt/β-连环蛋白信号通路的调控
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宿主转录组衍生的 HPV 致癌基因 E6*影响评分与头颈部癌症的致癌途径、肿瘤大小和生存存在显著关联。

Significant association between host transcriptome-derived HPV oncogene E6* influence score and carcinogenic pathways, tumor size, and survival in head and neck cancer.

机构信息

Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.

Kennedy Institute of Rheumatology, University of Oxford, United Kingdom.

出版信息

Head Neck. 2020 Sep;42(9):2375-2389. doi: 10.1002/hed.26244. Epub 2020 May 14.

DOI:10.1002/hed.26244
PMID:32406560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8052131/
Abstract

BACKGROUND

Human papillomavirus (HPV) oncogenes E6, E7, and shorter isoforms of E6 (E6*) are known carcinogenic factors in head and neck squamous cell carcinoma (HNSCC). Little is known regarding E6* functions.

METHODS

We analyzed RNA-seq data from 68 HNSCC HPV type 16-positive tumors to determine host genes and pathways associated with E6+E7 expression (E6E7) or the percent of full-length E6 (E6%FL). Influence scores of E6E7 and E6%FL were used to test for associations with clinical variables.

RESULTS

For E6E7, we recapitulated all major known affected pathways and revealed additional pathways. E6%FL was found to affect mitochondrial processes, and E6%FL influence score was significantly associated with overall survival and tumor size.

CONCLUSIONS

HPV E6E7 and E6* result in extensive, dose-dependent compensatory effects and dysregulation of key cancer pathways. The switch from E6 to E6* promotes oxidative phosphorylation, larger tumor size, and worse prognosis, potentially serving as a prognostic factor for HPV-positive HNSCC.

摘要

背景

人乳头瘤病毒(HPV)致癌基因 E6、E7 和 E6 的较短亚型(E6*)是头颈部鳞状细胞癌(HNSCC)的致癌因素。关于 E6* 的功能知之甚少。

方法

我们分析了 68 例 HPV 型 16 阳性 HNSCC 肿瘤的 RNA-seq 数据,以确定与 E6+E7 表达(E6E7)或全长 E6 的百分比(E6%FL)相关的宿主基因和途径。E6E7 和 E6%FL 的影响评分用于测试与临床变量的关联。

结果

对于 E6E7,我们重现了所有主要已知的受影响途径,并揭示了其他途径。发现 E6%FL 会影响线粒体过程,E6%FL 影响评分与总生存期和肿瘤大小显著相关。

结论

HPV E6E7 和 E6* 导致广泛的、剂量依赖性的补偿效应和关键癌症途径的失调。从 E6 到 E6* 的转变促进氧化磷酸化、更大的肿瘤大小和更差的预后,可能成为 HPV 阳性 HNSCC 的预后因素。