Identification of autophagy‐related gene and lncRNA signatures in the prognosis of HNSCC

Objective The aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC). Subjects and methods Differentially expressed autophagy‐related genes and autophagy‐related lncRNAs were identified by compari...

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Published inOral diseases Vol. 29; no. 1; pp. 138 - 153
Main Authors Li, Qilin, Wang, Jing, Meng, Xinyao, Chen, Weimin, Feng, Jiexiong, Mao, Jing
Format Journal Article
LanguageEnglish
Published Denmark Wiley Subscription Services, Inc 01.01.2023
Subjects
Autophagy
Autophagy - genetics
Cancer
Gene Expression Regulation, Neoplastic
Gene set enrichment analysis
Genes
Head & neck cancer
Head and neck carcinoma
Head and Neck Neoplasms - genetics
HNSCC
Humans
long non‐coding RNA
Medical prognosis
Non-coding RNA
Prognosis
RNA, Long Noncoding - genetics
Squamous cell carcinoma
Squamous Cell Carcinoma of Head and Neck - genetics
long non-coding RNA
autophagy
prognosis
HNSCC
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Abstract Objective The aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC). Subjects and methods Differentially expressed autophagy‐related genes and autophagy‐related lncRNAs were identified by comparing pare‐carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR‐lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR‐lncRNAs. Results Six ARGs and thirteen AR‐lncRNAs were identified in the ARG and AR‐lncRNA signatures, and overall survival (OS) in the high‐risk group was significantly shorter than the low‐risk group. ROC analysis showed the ARG and AR‐lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy‐related pathways are mainly enriched in the high‐risk group. Conclusions These findings indicated that our ARG signature and AR‐lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.
AbstractList The aim of this study was to identify prognostic autophagy-related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC).OBJECTIVEThe aim of this study was to identify prognostic autophagy-related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC).Differentially expressed autophagy-related genes and autophagy-related lncRNAs were identified by comparing pare-carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR-lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR-lncRNAs.SUBJECTS AND METHODSDifferentially expressed autophagy-related genes and autophagy-related lncRNAs were identified by comparing pare-carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR-lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR-lncRNAs.Six ARGs and thirteen AR-lncRNAs were identified in the ARG and AR-lncRNA signatures, and overall survival (OS) in the high-risk group was significantly shorter than the low-risk group. ROC analysis showed the ARG and AR-lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy-related pathways are mainly enriched in the high-risk group.RESULTSSix ARGs and thirteen AR-lncRNAs were identified in the ARG and AR-lncRNA signatures, and overall survival (OS) in the high-risk group was significantly shorter than the low-risk group. ROC analysis showed the ARG and AR-lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy-related pathways are mainly enriched in the high-risk group.These findings indicated that our ARG signature and AR-lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.CONCLUSIONSThese findings indicated that our ARG signature and AR-lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.
ObjectiveThe aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC).Subjects and methodsDifferentially expressed autophagy‐related genes and autophagy‐related lncRNAs were identified by comparing pare‐carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR‐lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR‐lncRNAs.ResultsSix ARGs and thirteen AR‐lncRNAs were identified in the ARG and AR‐lncRNA signatures, and overall survival (OS) in the high‐risk group was significantly shorter than the low‐risk group. ROC analysis showed the ARG and AR‐lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy‐related pathways are mainly enriched in the high‐risk group.ConclusionsThese findings indicated that our ARG signature and AR‐lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.
The aim of this study was to identify prognostic autophagy-related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC). Differentially expressed autophagy-related genes and autophagy-related lncRNAs were identified by comparing pare-carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR-lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR-lncRNAs. Six ARGs and thirteen AR-lncRNAs were identified in the ARG and AR-lncRNA signatures, and overall survival (OS) in the high-risk group was significantly shorter than the low-risk group. ROC analysis showed the ARG and AR-lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy-related pathways are mainly enriched in the high-risk group. These findings indicated that our ARG signature and AR-lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.
Objective The aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma (HNSCC). Subjects and methods Differentially expressed autophagy‐related genes and autophagy‐related lncRNAs were identified by comparing pare‐carcinoma and carcinoma samples of HNSCC. And then, we constructed an ARG and an AR‐lncRNA signature risk score. Receiver operating characteristic (ROC) curve analyses were performed to assess the prognostic prediction capacity. Gene Set Enrichment Analysis (GSEA) and Gene Ontology (GO) functional annotation were used to analysis the functions of ARGs and AR‐lncRNAs. Results Six ARGs and thirteen AR‐lncRNAs were identified in the ARG and AR‐lncRNA signatures, and overall survival (OS) in the high‐risk group was significantly shorter than the low‐risk group. ROC analysis showed the ARG and AR‐lncRNA signatures have excellent ability of predicting the total OS of patients with HNSCC. What's more, GSEA and GO functional annotation proved that autophagy‐related pathways are mainly enriched in the high‐risk group. Conclusions These findings indicated that our ARG signature and AR‐lncRNA signature could be considered to predict the prognosis of patients with HNSCC and provide a deep understanding of the biological mechanisms of autophagy in HNSCC.
Author Chen, Weimin
Li, Qilin
Mao, Jing
Feng, Jiexiong
Wang, Jing
Meng, Xinyao
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Cites_doi 10.1111/jcmm.14394
10.1016/j.oraloncology.2013.10.003
10.7150/thno.44251
10.1245/s10434‐019‐07287‐x
10.3322/caac.21492
10.1186/s13046‐018‐0993‐y
10.1002/hed.25172
10.1016/j.eururo.2015.01.005
10.1038/s41420‐020‐00294‐y
10.1172/JCI73941
10.1042/BSR20181367
10.1089/hgtb.2019.115
10.1016/j.arcmed.2020.09.009
10.1016/j.ygeno.2020.11.017
10.1186/s12943‐017‐0756‐y
10.1200/JCO.2012.44.0164
10.4161/auto.23486
10.1080/13543784.2019.1581172
10.1016/j.eururo.2014.06.053
10.1111/odi.12254
10.1590/1414‐431x20187080
10.1016/j.oraloncology.2015.12.007
10.4161/auto.32200
10.3390/cells9041063
10.1186/s12885‐020‐07303‐4
10.1111/odi.13355
10.1016/j.canlet.2018.03.024
10.7150/thno.34887
10.3322/caac.21551
10.1038/cdd.2016.111
10.15252/embj.201593596
10.1016/S1470‐2045(19)30306‐7
10.1080/15384047.2019.1617571
10.1007/978‐3‐319‐43580‐0_18
10.1186/s12967‐020‐02323‐x
10.1016/j.ygeno.2020.10.008
10.1038/s41571‐019‐0227‐z
10.1158/0008‐5472.CAN‐17‐1077
10.18632/aging.102716
10.1038/s41586‐020‐1996‐3
10.1016/j.lungcan.2015.07.008
10.3748/wjg.v17.i19.2389
10.1080/15548627.2020.1826690
10.12659/MSM.910773
10.1016/j.canlet.2019.02.052
10.1038/s41388‐017‐0046‐6
10.1038/s41388‐019‐0973‐5
10.1186/s12935‐017‐0463‐1
10.1080/15548627.2019.1639302
10.1080/15548627.2015.1017184
10.1038/emboj.2012.151
10.1097/MD.0000000000021163
10.1002/ijc.28847
10.1111/odi.13045
10.1186/s40425‐019‐0662‐5
10.1186/s13046‐019‐1343‐4
10.1200/JCO.19.03156
10.1186/s12935‐020‐01267‐y
10.2147/CMAR.S253575
10.3322/caac.21565
10.4161/auto.7.7.15454
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Keywords long non-coding RNA
autophagy
prognosis
HNSCC
Language English
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References 2020; 20
2019; 12
2019; 15
2019; 16
2020; 12
2020; 99
2020; 10
2011; 17
2014; 66
2016; 35
2013; 9
2020; 18
2020; 6
2019; 20
2020; 51
2015; 136
2017; 77
2019; 23
2019; 26
2020; 9
2019; 69
2020; 578
2019; 28
2015; 90
2014; 50
2018; 37
2014; 10
2017; 206
2019; 7
2019; 9
2018; 425
2019; 30
2015; 125
2017; 24
2015; 11
2016; 54
2020; 39
2019; 39
2019; 38
2020; 38
2012; 31
2011; 7
2018; 68
2018; 24
2015; 67
2018; 17
2019; 41
2017; 17
2020
2013; 31
2015; 21
2020; 26
2018; 51
2020; 113
2018; 10
2019; 451
e_1_2_9_31_1
e_1_2_9_52_1
e_1_2_9_50_1
e_1_2_9_10_1
e_1_2_9_35_1
e_1_2_9_56_1
e_1_2_9_12_1
e_1_2_9_33_1
e_1_2_9_54_1
e_1_2_9_39_1
e_1_2_9_16_1
e_1_2_9_37_1
e_1_2_9_58_1
e_1_2_9_18_1
e_1_2_9_41_1
e_1_2_9_64_1
e_1_2_9_20_1
e_1_2_9_62_1
e_1_2_9_22_1
e_1_2_9_45_1
e_1_2_9_24_1
e_1_2_9_43_1
e_1_2_9_8_1
e_1_2_9_6_1
e_1_2_9_4_1
e_1_2_9_60_1
e_1_2_9_2_1
e_1_2_9_26_1
e_1_2_9_49_1
e_1_2_9_28_1
e_1_2_9_47_1
e_1_2_9_30_1
e_1_2_9_53_1
e_1_2_9_51_1
e_1_2_9_11_1
e_1_2_9_34_1
e_1_2_9_57_1
e_1_2_9_13_1
e_1_2_9_32_1
e_1_2_9_55_1
Cui L. (e_1_2_9_14_1) 2019; 12
e_1_2_9_15_1
e_1_2_9_38_1
e_1_2_9_17_1
e_1_2_9_36_1
e_1_2_9_19_1
e_1_2_9_42_1
Xu W. (e_1_2_9_59_1) 2018; 10
e_1_2_9_63_1
e_1_2_9_40_1
e_1_2_9_61_1
e_1_2_9_21_1
e_1_2_9_46_1
e_1_2_9_23_1
e_1_2_9_44_1
e_1_2_9_7_1
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e_1_2_9_29_1
References_xml – volume: 31
  start-page: 543
  issue: 5
  year: 2013
  end-page: 550
  article-title: Deintensification candidate subgroups in human papillomavirus‐related oropharyngeal cancer according to minimal risk of distant metastasis
  publication-title: Journal of Clinical Oncology
– volume: 206
  start-page: 233
  year: 2017
  end-page: 242
  article-title: Predictive factors for outcome and quality of life in HPV‐positive and HPV‐negative HNSCC
  publication-title: Recent Results in Cancer Research
– volume: 17
  start-page: 6
  issue: 1
  year: 2018
  article-title: STAT3‐induced lncRNA HAGLROS overexpression contributes to the malignant progression of gastric cancer cells via mTOR signal‐mediated inhibition of autophagy
  publication-title: Molecular Cancer
– volume: 12
  start-page: 2989
  issue: 8
  year: 2019
  end-page: 2996
  article-title: The autophagy‐related genes Beclin1 and LC3 in the prognosis of pancreatic cancer
  publication-title: International Journal of Clinical and Experimental Pathology
– volume: 50
  start-page: 19
  issue: 1
  year: 2014
  end-page: 26
  article-title: Combination antiangiogenic therapy and radiation in head and neck cancers
  publication-title: Oral Oncology
– volume: 99
  issue: 30
  year: 2020
  article-title: An autophagy‐related model of 4 key genes for predicting prognosis of patients with laryngeal cancer
  publication-title: Medicine (Baltimore)
– volume: 77
  start-page: 6679
  issue: 23
  year: 2017
  end-page: 6691
  article-title: Secretory autophagy in cancer‐associated fibroblasts promotes head and neck cancer progression and offers a novel therapeutic target
  publication-title: Cancer Research
– volume: 578
  start-page: 449
  issue: 7795
  year: 2020
  end-page: 454
  article-title: Loss of p53 drives neuron reprogramming in head and neck cancer
  publication-title: Nature
– volume: 12
  start-page: 1843
  issue: 2
  year: 2020
  end-page: 1856
  article-title: Long non‐coding RNA PSMA3‐AS1 promotes malignant phenotypes of esophageal cancer by modulating the miR‐101/EZH2 axis as a ceRNA
  publication-title: Aging (Albany NY)
– volume: 7
  start-page: 184
  issue: 1
  year: 2019
  article-title: The Society for Immunotherapy of Cancer consensus statement on immunotherapy for the treatment of squamous cell carcinoma of the head and neck (HNSCC)
  publication-title: Journal for ImmunoTherapy of Cancer
– volume: 9
  start-page: 1063
  issue: 4
  year: 2020
  article-title: The role of autophagy in pancreatic cancer: From bench to the dark bedside
  publication-title: Cells
– volume: 136
  start-page: 1494
  issue: 7
  year: 2015
  end-page: 1503
  article-title: Treatment de‐escalation in HPV‐positive oropharyngeal carcinoma: Ongoing trials, critical issues and perspectives
  publication-title: International Journal of Cancer
– volume: 10
  start-page: 1895
  issue: 11
  year: 2014
  end-page: 1905
  article-title: Vacuolin‐1 potently and reversibly inhibits autophagosome‐lysosome fusion by activating RAB5A
  publication-title: Autophagy
– volume: 51
  issue: 6
  year: 2018
  article-title: LncRNA HULC mediates radioresistance via autophagy in prostate cancer cells
  publication-title: Brazilian Journal of Medical and Biological Research
– volume: 38
  start-page: 2427
  issue: 21
  year: 2020
  end-page: 2437
  article-title: Safety and efficacy of pembrolizumab with chemoradiotherapy in locally advanced head and neck squamous cell carcinoma: A phase IB study
  publication-title: Journal of Clinical Oncology
– volume: 69
  start-page: 7
  issue: 1
  year: 2019
  end-page: 34
  article-title: Cancer statistics, 2019
  publication-title: CA: A Cancer Journal for Clinicians
– volume: 451
  start-page: 34
  year: 2019
  end-page: 47
  article-title: Blocking autophagy flux promotes interferon‐alpha‐mediated apoptosis in head and neck squamous cell carcinoma
  publication-title: Cancer Letters
– volume: 17
  start-page: 2389
  issue: 19
  year: 2011
  end-page: 2396
  article-title: CXCR4/SDF‐1 axis is involved in lymph node metastasis of gastric carcinoma
  publication-title: World Journal of Gastroenterology
– volume: 23
  start-page: 4711
  issue: 7
  year: 2019
  end-page: 4722
  article-title: Wnt3a promotes radioresistance via autophagy in squamous cell carcinoma of the head and neck
  publication-title: Journal of Cellular and Molecular Medicine
– volume: 7
  start-page: 760
  issue: 7
  year: 2011
  end-page: 770
  article-title: The acquisition of resistance to TNFalpha in breast cancer cells is associated with constitutive activation of autophagy as revealed by a transcriptome analysis using a custom microarray
  publication-title: Autophagy
– volume: 24
  start-page: 212
  issue: 2
  year: 2017
  end-page: 224
  article-title: The lncRNA HOTAIRM1 regulates the degradation of PML‐RARA oncoprotein and myeloid cell differentiation by enhancing the autophagy pathway
  publication-title: Cell Death and Differentiation
– volume: 6
  start-page: 59
  year: 2020
  article-title: Development and validation of prognostic index based on autophagy‐related genes in patient with head and neck squamous cell carcinoma
  publication-title: Cell Death Discovery
– volume: 54
  start-page: 1
  year: 2016
  end-page: 6
  article-title: The role of autophagy in squamous cell carcinoma of the head and neck
  publication-title: Oral Oncology
– volume: 24
  start-page: 8250
  year: 2018
  end-page: 8263
  article-title: Functional long noncoding RNAs (lncRNAs) in clear cell kidney carcinoma revealed by reconstruction and comprehensive analysis of the lncRNA‐miRNA‐mRNA regulatory network
  publication-title: Medical Science Monitor
– volume: 113
  start-page: 1166
  issue: 1
  year: 2020
  end-page: 1175
  article-title: Development and validation of a novel survival model for head and neck squamous cell carcinoma based on autophagy‐related genes
  publication-title: Genomics
– volume: 9
  start-page: 5134
  issue: 18
  year: 2019
  end-page: 5148
  article-title: C‐myc/miR‐150/EPG5 axis mediated dysfunction of autophagy promotes development of non‐small cell lung cancer
  publication-title: Theranostics
– volume: 69
  start-page: 363
  issue: 5
  year: 2019
  end-page: 385
  article-title: Cancer treatment and survivorship statistics, 2019
  publication-title: CA: A Cancer Journal for Clinicians
– volume: 113
  start-page: 767
  issue: 1
  year: 2020
  end-page: 777
  article-title: A risk signature of three autophagy‐related genes for predicting lower grade glioma survival is associated with tumor immune microenvironment
  publication-title: Genomics
– volume: 38
  start-page: 340
  issue: 1
  year: 2019
  article-title: TFEB‐driven autophagy potentiates TGF‐beta induced migration in pancreatic cancer cells
  publication-title: Journal of Experimental & Clinical Cancer Research
– volume: 11
  start-page: 503
  issue: 3
  year: 2015
  end-page: 515
  article-title: Binding of the pathogen receptor HSP90AA1 to avibirnavirus VP2 induces autophagy by inactivating the AKT‐MTOR pathway
  publication-title: Autophagy
– volume: 68
  start-page: 394
  issue: 6
  year: 2018
  end-page: 424
  article-title: Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
  publication-title: CA: A Cancer Journal for Clinicians
– volume: 41
  start-page: 511
  issue: 2
  year: 2019
  end-page: 521
  article-title: Prognosis of subglottic carcinoma: Is it really worse?
  publication-title: Head and Neck
– volume: 17
  start-page: 99
  year: 2017
  article-title: Correction to: The role of ppargamma and autophagy in ros production, lipid droplets biogenesis and its involvement with colorectal cancer cells modulation
  publication-title: Cancer Cell International
– volume: 15
  start-page: 1850
  issue: 10
  year: 2019
  end-page: 1851
  article-title: SLC3A2/CD98hc, autophagy and tumor radioresistance: A link confirmed
  publication-title: Autophagy
– volume: 10
  start-page: 11549
  issue: 25
  year: 2020
  end-page: 11561
  article-title: CXCR4 induces cell autophagy and maintains EBV latent infection in EBVaGC
  publication-title: Theranostics
– volume: 51
  start-page: 860
  issue: 8
  year: 2020
  end-page: 867
  article-title: Development of a prognostic signature based on autophagy‐related genes for head and neck squamous cell carcinoma
  publication-title: Archives of Medical Research
– volume: 37
  start-page: 320
  issue: 1
  year: 2018
  article-title: Novel role of miR‐133a‐3p in repressing gastric cancer growth and metastasis via blocking autophagy‐mediated glutaminolysis
  publication-title: Journal of Experimental & Clinical Cancer Research
– volume: 39
  start-page: 151
  issue: 1
  year: 2020
  end-page: 163
  article-title: ALK(ATI) interacts with c‐Myc and promotes cancer stem cell‐like properties in sarcoma
  publication-title: Oncogene
– volume: 20
  start-page: e404
  issue: 8
  year: 2019
  end-page: e416
  article-title: Radioimmunotherapy for the treatment of head and neck cancer
  publication-title: The Lancet Oncology
– volume: 39
  start-page: BSR20181367
  issue: 6
  year: 2019
  article-title: Suppression of lncRNA RMRP ameliorates oxygen‐glucose deprivation/re‐oxygenation‐induced neural cells injury by inhibiting autophagy and PI3K/Akt/mTOR‐mediated apoptosis
  publication-title: Bioscience Reports
– volume: 16
  start-page: 669
  issue: 11
  year: 2019
  end-page: 683
  article-title: The changing therapeutic landscape of head and neck cancer
  publication-title: Nature Reviews. Clinical Oncology
– volume: 28
  start-page: 351
  issue: 4
  year: 2019
  end-page: 363
  article-title: Investigational multitargeted kinase inhibitors in development for head and neck neoplasms
  publication-title: Expert Opinion on Investigational Drugs
– volume: 35
  start-page: 866
  issue: 8
  year: 2016
  end-page: 880
  article-title: USP19 modulates autophagy and antiviral immune responses by deubiquitinating Beclin‐1
  publication-title: EMBO Journal
– volume: 26
  start-page: 259
  issue: 2
  year: 2020
  end-page: 269
  article-title: The role of autophagy in the pathogenesis of periodontal disease
  publication-title: Oral Diseases
– volume: 67
  start-page: 913
  issue: 5
  year: 2015
  end-page: 924
  article-title: EAU guidelines on renal cell carcinoma: 2014 update
  publication-title: European Urology
– volume: 10
  start-page: 1229
  issue: 4
  year: 2018
  end-page: 1236
  article-title: Rab5a suppresses autophagy to promote drug resistance in cancer cells
  publication-title: American Journal of Translational Research
– volume: 12
  start-page: 5277
  year: 2020
  end-page: 5283
  article-title: LncRNA PSMA3‐AS1 promotes lung cancer growth and invasion via sponging MiR‐4504
  publication-title: Cancer Management and Research
– volume: 9
  start-page: 612
  issue: 4
  year: 2013
  end-page: 614
  article-title: PERK‐ing up autophagy during MYC‐induced tumorigenesis
  publication-title: Autophagy
– volume: 30
  start-page: 226
  issue: 6
  year: 2019
  end-page: 234
  article-title: LINC00958 accelerates cell proliferation and migration in non‐small cell lung cancer through JNK/c‐JUN signaling
  publication-title: Human Gene Therapy Methods
– volume: 20
  start-page: 178
  year: 2020
  article-title: Identification and validation of an individualized autophagy‐clinical prognostic index in gastric cancer patients
  publication-title: Cancer Cell International
– volume: 26
  start-page: 1165
  issue: 6
  year: 2020
  end-page: 1174
  article-title: Autophagy inhibits TLR4‐mediated invasiveness of oral cancer cells via the NF‐kappaB pathway
  publication-title: Oral Diseases
– volume: 20
  start-page: 797
  issue: 1
  year: 2020
  article-title: Prognostic significance of autophagy‐related genes within esophageal carcinoma
  publication-title: BMC Cancer
– volume: 66
  start-page: 936
  issue: 5
  year: 2014
  end-page: 948
  article-title: Systematic evaluation of the prognostic impact and intratumour heterogeneity of clear cell renal cell carcinoma biomarkers
  publication-title: European Urology
– volume: 31
  start-page: 2852
  issue: 13
  year: 2012
  end-page: 2868
  article-title: Pex3‐anchored Atg36 tags peroxisomes for degradation in Saccharomyces cerevisiae
  publication-title: EMBO Journal
– volume: 37
  start-page: 1142
  issue: 9
  year: 2018
  end-page: 1158
  article-title: Dual role of autophagy in hallmarks of cancer
  publication-title: Oncogene
– start-page: 1
  year: 2020
  end-page: 18
  article-title: Secretory autophagy machinery and vesicular trafficking are involved in HMGB1 secretion
  publication-title: Autophagy
– volume: 26
  start-page: 2294
  issue: 7
  year: 2019
  end-page: 2303
  article-title: All‐exon TP53 sequencing and protein phenotype analysis accurately predict clinical outcome after surgical treatment of head and neck squamous cell carcinoma
  publication-title: Annals of Surgical Oncology
– volume: 20
  start-page: 1270
  issue: 9
  year: 2019
  end-page: 1280
  article-title: LINC00958 regulated miR‐627‐5p/YBX2 axis to facilitate cell proliferation and migration in oral squamous cell carcinoma
  publication-title: Cancer Biology & Therapy
– volume: 90
  start-page: 98
  issue: 1
  year: 2015
  end-page: 105
  article-title: Increased expression of transcription factor EB (TFEB) is associated with autophagy, migratory phenotype and poor prognosis in non‐small cell lung cancer
  publication-title: Lung Cancer
– volume: 18
  start-page: 160
  issue: 1
  year: 2020
  article-title: Development of an autophagy‐related gene expression signature for prognosis prediction in prostate cancer patients
  publication-title: Journal of Translational Medicine
– volume: 425
  start-page: 1
  year: 2018
  end-page: 12
  article-title: CXCR4‐mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance
  publication-title: Cancer Letters
– volume: 125
  start-page: 42
  issue: 1
  year: 2015
  end-page: 46
  article-title: The role for autophagy in cancer
  publication-title: Journal of Clinical Investigation
– volume: 21
  start-page: 283
  issue: 3
  year: 2015
  end-page: 291
  article-title: Role of autophagy in head and neck cancer and therapeutic resistance
  publication-title: Oral Diseases
– ident: e_1_2_9_30_1
  doi: 10.1111/jcmm.14394
– ident: e_1_2_9_23_1
  doi: 10.1016/j.oraloncology.2013.10.003
– ident: e_1_2_9_56_1
  doi: 10.7150/thno.44251
– ident: e_1_2_9_33_1
  doi: 10.1245/s10434‐019‐07287‐x
– ident: e_1_2_9_4_1
  doi: 10.3322/caac.21492
– ident: e_1_2_9_61_1
  doi: 10.1186/s13046‐018‐0993‐y
– volume: 10
  start-page: 1229
  issue: 4
  year: 2018
  ident: e_1_2_9_59_1
  article-title: Rab5a suppresses autophagy to promote drug resistance in cancer cells
  publication-title: American Journal of Translational Research
– ident: e_1_2_9_11_1
  doi: 10.1002/hed.25172
– ident: e_1_2_9_38_1
  doi: 10.1016/j.eururo.2015.01.005
– ident: e_1_2_9_17_1
  doi: 10.1038/s41420‐020‐00294‐y
– ident: e_1_2_9_57_1
  doi: 10.1172/JCI73941
– ident: e_1_2_9_63_1
  doi: 10.1042/BSR20181367
– ident: e_1_2_9_41_1
  doi: 10.1089/hgtb.2019.115
– ident: e_1_2_9_29_1
  doi: 10.1016/j.arcmed.2020.09.009
– ident: e_1_2_9_51_1
  doi: 10.1016/j.ygeno.2020.11.017
– ident: e_1_2_9_8_1
  doi: 10.1186/s12943‐017‐0756‐y
– ident: e_1_2_9_47_1
  doi: 10.1200/JCO.2012.44.0164
– ident: e_1_2_9_15_1
  doi: 10.4161/auto.23486
– ident: e_1_2_9_55_1
  doi: 10.1080/13543784.2019.1581172
– ident: e_1_2_9_20_1
  doi: 10.1016/j.eururo.2014.06.053
– ident: e_1_2_9_52_1
  doi: 10.1111/odi.12254
– ident: e_1_2_9_6_1
  doi: 10.1590/1414‐431x20187080
– ident: e_1_2_9_12_1
  doi: 10.1016/j.oraloncology.2015.12.007
– ident: e_1_2_9_39_1
  doi: 10.4161/auto.32200
– ident: e_1_2_9_19_1
  doi: 10.3390/cells9041063
– ident: e_1_2_9_5_1
  doi: 10.1186/s12885‐020‐07303‐4
– ident: e_1_2_9_34_1
  doi: 10.1111/odi.13355
– ident: e_1_2_9_26_1
  doi: 10.1016/j.canlet.2018.03.024
– ident: e_1_2_9_36_1
  doi: 10.7150/thno.34887
– ident: e_1_2_9_53_1
  doi: 10.3322/caac.21551
– ident: e_1_2_9_9_1
  doi: 10.1038/cdd.2016.111
– ident: e_1_2_9_28_1
  doi: 10.15252/embj.201593596
– ident: e_1_2_9_31_1
  doi: 10.1016/S1470‐2045(19)30306‐7
– ident: e_1_2_9_7_1
  doi: 10.1080/15384047.2019.1617571
– volume: 12
  start-page: 2989
  issue: 8
  year: 2019
  ident: e_1_2_9_14_1
  article-title: The autophagy‐related genes Beclin1 and LC3 in the prognosis of pancreatic cancer
  publication-title: International Journal of Clinical and Experimental Pathology
– ident: e_1_2_9_22_1
  doi: 10.1007/978‐3‐319‐43580‐0_18
– ident: e_1_2_9_25_1
  doi: 10.1186/s12967‐020‐02323‐x
– ident: e_1_2_9_37_1
  doi: 10.1016/j.ygeno.2020.10.008
– ident: e_1_2_9_13_1
  doi: 10.1038/s41571‐019‐0227‐z
– ident: e_1_2_9_46_1
  doi: 10.1158/0008‐5472.CAN‐17‐1077
– ident: e_1_2_9_49_1
  doi: 10.18632/aging.102716
– ident: e_1_2_9_2_1
  doi: 10.1038/s41586‐020‐1996‐3
– ident: e_1_2_9_18_1
  doi: 10.1016/j.lungcan.2015.07.008
– ident: e_1_2_9_62_1
  doi: 10.3748/wjg.v17.i19.2389
– ident: e_1_2_9_32_1
  doi: 10.1080/15548627.2020.1826690
– ident: e_1_2_9_64_1
  doi: 10.12659/MSM.910773
– ident: e_1_2_9_60_1
  doi: 10.1016/j.canlet.2019.02.052
– ident: e_1_2_9_54_1
  doi: 10.1038/s41388‐017‐0046‐6
– ident: e_1_2_9_58_1
  doi: 10.1038/s41388‐019‐0973‐5
– ident: e_1_2_9_3_1
  doi: 10.1186/s12935‐017‐0463‐1
– ident: e_1_2_9_16_1
  doi: 10.1080/15548627.2019.1639302
– ident: e_1_2_9_24_1
  doi: 10.1080/15548627.2015.1017184
– ident: e_1_2_9_44_1
  doi: 10.1038/emboj.2012.151
– ident: e_1_2_9_40_1
  doi: 10.1097/MD.0000000000021163
– ident: e_1_2_9_43_1
  doi: 10.1002/ijc.28847
– ident: e_1_2_9_27_1
  doi: 10.1111/odi.13045
– ident: e_1_2_9_10_1
  doi: 10.1186/s40425‐019‐0662‐5
– ident: e_1_2_9_21_1
  doi: 10.1186/s13046‐019‐1343‐4
– ident: e_1_2_9_48_1
  doi: 10.1200/JCO.19.03156
– ident: e_1_2_9_50_1
  doi: 10.1186/s12935‐020‐01267‐y
– ident: e_1_2_9_35_1
  doi: 10.2147/CMAR.S253575
– ident: e_1_2_9_42_1
  doi: 10.3322/caac.21565
– ident: e_1_2_9_45_1
  doi: 10.4161/auto.7.7.15454
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Snippet Objective The aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell...
The aim of this study was to identify prognostic autophagy-related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell carcinoma...
ObjectiveThe aim of this study was to identify prognostic autophagy‐related genes and lncRNAs to predict clinical outcomes in head and neck squamous cell...
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wiley
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StartPage 138
SubjectTerms Autophagy
Autophagy - genetics
Cancer
Gene Expression Regulation, Neoplastic
Gene set enrichment analysis
Genes
Head & neck cancer
Head and neck carcinoma
Head and Neck Neoplasms - genetics
HNSCC
Humans
long non‐coding RNA
Medical prognosis
Non-coding RNA
Prognosis
RNA, Long Noncoding - genetics
Squamous cell carcinoma
Squamous Cell Carcinoma of Head and Neck - genetics
Title Identification of autophagy‐related gene and lncRNA signatures in the prognosis of HNSCC
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fodi.13889
https://www.ncbi.nlm.nih.gov/pubmed/33901303
https://www.proquest.com/docview/2755408496
https://www.proquest.com/docview/2518969500
Volume 29
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