Single cell transcriptomic analysis of HPV16-infected epithelium identifies a keratinocyte subpopulation implicated in cancer
-
Published:2023-04-08
Issue:1
Volume:14
Page:
-
ISSN:2041-1723
-
Container-title:Nature Communications
-
language:en
-
Short-container-title:Nat Commun
Author:
Bedard Mary C., Chihanga Tafadzwa, Carlile Adrean, Jackson RobertORCID, Brusadelli Marion G., Lee Denis, VonHandorf Andrew, Rochman MarkORCID, Dexheimer Phillip J.ORCID, Chalmers JeffreyORCID, Nuovo Gerard, Lehn MariaORCID, Williams David E. J., Kulkarni Aditi, Carey Molly, Jackson Amanda, Billingsley Caroline, Tang Alice, Zender Chad, Patil Yash, Wise-Draper Trisha M., Herzog Thomas J., Ferris Robert L., Kendler Ady, Aronow Bruce J.ORCID, Kofron Matthew, Rothenberg Marc E.ORCID, Weirauch Matthew T., Van Doorslaer KoenraadORCID, Wikenheiser-Brokamp Kathryn A.ORCID, Lambert Paul F., Adam MikeORCID, Steven Potter S.ORCID, Wells Susanne I.ORCID
Abstract
AbstractPersistent HPV16 infection is a major cause of the global cancer burden. The viral life cycle is dependent on the differentiation program of stratified squamous epithelium, but the landscape of keratinocyte subpopulations which support distinct phases of the viral life cycle has yet to be elucidated. Here, single cell RNA sequencing of HPV16 infected compared to uninfected organoids identifies twelve distinct keratinocyte populations, with a subset mapped to reconstruct their respective 3D geography in stratified squamous epithelium. Instead of conventional terminally differentiated cells, an HPV-reprogrammed keratinocyte subpopulation (HIDDEN cells) forms the surface compartment and requires overexpression of the ELF3/ESE-1 transcription factor. HIDDEN cells are detected throughout stages of human carcinogenesis including primary human cervical intraepithelial neoplasias and HPV positive head and neck cancers, and a possible role in promoting viral carcinogenesis is supported by TCGA analyses. Single cell transcriptome information on HPV-infected versus uninfected epithelium will enable broader studies of the role of individual keratinocyte subpopulations in tumor virus infection and cancer evolution.
Funder
U.S. Department of Health & Human Services | NIH | National Institute of Environmental Health Sciences CancerFreeKids The BI05 Institute State of Arizona Improving Health TRIF U.S. Department of Health & Human Services | NIH | National Cancer Institute
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary
Reference94 articles.
1. zur Hausen, H. The search for infectious causes of human cancers: where and why (Nobel lecture). Angew. Chem. Int. Ed. Engl. 48, 5798–5808 (2009). 2. McBride, A. A. Human papillomaviruses: diversity, infection and host interactions. Nat. Rev. Microbiol. 20, 95–108 (2022). 3. Della Fera, A. N. et al. Persistent human papillomavirus infection. Viruses 13, 321 (2021). 4. Bosch, F. X. et al. The causal relation between human papillomavirus and cervical cancer. J. Clin. Pathol. 55, 244–265 (2002). 5. Serrano, B. et al. Epidemiology and burden of HPV-related disease. Best Pract. Res. Clin. Obstet. Gynaecol. 47, 14–26 (2018).
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|