Ovarian cancer-derived copy number alterations signatures are prognostic in chemoradiotherapy-treated head and neck squamous cell carcinoma.
Adult
Aged
Aged, 80 and over
Biomarkers, Tumor
/ genetics
Biopsy
Chemoradiotherapy
Cisplatin
/ pharmacology
DNA Copy Number Variations
Datasets as Topic
Drug Resistance, Neoplasm
/ genetics
Female
Follow-Up Studies
Gene Expression Profiling
Head and Neck Neoplasms
/ genetics
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Netherlands
/ epidemiology
Ovarian Neoplasms
/ genetics
Prognosis
Progression-Free Survival
RNA-Seq
Retrospective Studies
Squamous Cell Carcinoma of Head and Neck
/ genetics
Transcriptome
/ genetics
Whole Genome Sequencing
HNSCC
chemoradiotherapy
cisplatin
copy number alterations
head and neck squamous cell carcinoma
prognosis
Journal
International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124
Informations de publication
Date de publication:
15 09 2020
15 09 2020
Historique:
received:
29
10
2019
revised:
17
01
2020
accepted:
11
02
2020
pubmed:
14
3
2020
medline:
15
4
2021
entrez:
14
3
2020
Statut:
ppublish
Résumé
DNA copy number alterations (CNAs) are frequent in cancer, and recently developed CNA signatures revealed their value in molecular tumor stratification for patient prognosis and platinum resistance prediction in ovarian cancer. Head and neck squamous cell carcinoma (HNSCC) is also characterized by high CNAs. In this study, we determined CNA in 173 human papilloma virus-negative HNSCC from a Dutch multicenter cohort by low-coverage whole genome sequencing and tested the prognostic value of seven cancer-derived CNA signatures for these cisplatin- and radiotherapy-treated patients. We find that a high CNA signature 1 (s1) score is associated with low values for all other signatures and better patient outcomes in the Dutch cohorts and The Cancer Genome Atlas HNSCC data set. High s5 and s7 scores are associated with increased distant metastasis rates and high s6 scores with poor overall survival. High cumulative cisplatin doses result in improved outcomes in chemoradiotherapy-treated HNSCC patients. Here we find that tumors high in s1 or low in s6 are most responsive to a change in cisplatin dose. High s5 values, however, significantly increase the risk for metastasis in patients with low cumulative cisplatin doses. Together this suggests that the processes causing these CNA signatures affect cisplatin response in HNSCC. In conclusion, CNA signatures derived from a different cancer type were prognostic and associated with cisplatin response in HNSCC, suggesting they represent underlying molecular processes that define patient outcome.
Identifiants
pubmed: 32167160
doi: 10.1002/ijc.32962
pmc: PMC7496441
doi:
Substances chimiques
Biomarkers, Tumor
0
Cisplatin
Q20Q21Q62J
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1732-1739Informations de copyright
© 2020 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
Références
Source Code Biol Med. 2016 Dec 15;11:13
pubmed: 27999612
Cancer Res. 2015 Sep 1;75(17):3543-53
pubmed: 26122845
Science. 2011 Aug 26;333(6046):1154-7
pubmed: 21798897
Nat Rev Cancer. 2018 May;18(5):269-282
pubmed: 29497144
Nat Commun. 2018 Aug 17;9(1):3292
pubmed: 30120226
Genome Res. 2014 Dec;24(12):2022-32
pubmed: 25236618
Nat Genet. 2018 Sep;50(9):1262-1270
pubmed: 30104763
Oral Oncol. 2018 Jul;82:195
pubmed: 29859830
Bioinformatics. 2019 Aug 15;35(16):2847-2849
pubmed: 30596895
Eur J Cancer. 2018 Mar;91:47-55
pubmed: 29331751
Radiother Oncol. 2009 Jul;92(1):4-14
pubmed: 19446902
Head Neck. 2004 Jun;26(6):485-93
pubmed: 15162349
Oncotarget. 2018 Apr 6;9(26):18198-18213
pubmed: 29719599
Nature. 2015 Jan 29;517(7536):576-82
pubmed: 25631445
Int J Cancer. 2019 Dec 1;145(11):3152-3162
pubmed: 31093971
Science. 2011 Aug 26;333(6046):1157-60
pubmed: 21798893
Nat Rev Cancer. 2011 Jan;11(1):9-22
pubmed: 21160525
Front Oncol. 2020 Jan 10;9:1470
pubmed: 31998639
Clin Cancer Res. 2016 Apr 15;22(8):2062-73
pubmed: 26603260
Cancer Res. 2019 Nov 1;79(21):5597-5611
pubmed: 31515237
Oral Oncol. 2018 Jun;81:35-44
pubmed: 29884412
Eur Arch Otorhinolaryngol. 2017 Oct;274(10):3757-3765
pubmed: 28755023
Cell. 2018 Apr 5;173(2):400-416.e11
pubmed: 29625055