CXCL14 suppresses human papillomavirus-associated head and neck cancer through antigen-specific CD8


Journal

Oncogene
ISSN: 1476-5594
Titre abrégé: Oncogene
Pays: England
ID NLM: 8711562

Informations de publication

Date de publication:
11 2019
Historique:
received: 01 02 2019
accepted: 26 05 2019
revised: 23 05 2019
pubmed: 17 8 2019
medline: 29 2 2020
entrez: 17 8 2019
Statut: ppublish

Résumé

Evasion of the host immune responses is critical for both persistent human papillomavirus (HPV) infection and associated cancer progression. We have previously shown that expression of the homeostatic chemokine CXCL14 is significantly downregulated by the HPV oncoprotein E7 during cancer progression. Restoration of CXCL14 expression in HPV-positive head and neck cancer (HNC) cells dramatically suppresses tumor growth and increases survival through an immune-dependent mechanism in mice. Although CXCL14 recruits natural killer (NK) and T cells to the tumor microenvironment, the mechanism by which CXCL14 mediates tumor suppression through NK and/or T cells remained undefined. Here we report that CD8

Identifiants

pubmed: 31417179
doi: 10.1038/s41388-019-0911-6
pii: 10.1038/s41388-019-0911-6
pmc: PMC6856418
mid: NIHMS1530690
doi:

Substances chimiques

CXCL14 protein, mouse 0
Chemokines, CXC 0
Histocompatibility Antigens Class I 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7166-7180

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM103548
Pays : United States
Organisme : NIDCR NIH HHS
ID : R01 DE026125
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI052066
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008730
Pays : United States

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Auteurs

Joseph A Westrich (JA)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado, USA.

Daniel W Vermeer (DW)

Cancer Biology Research Center, Sanford Research, Sioux Falls, SD, 57104, USA.

Alexa Silva (A)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

Stephanie Bonney (S)

Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

Jennifer N Berger (JN)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

Louis Cicchini (L)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

Robert O Greer (RO)

Departments of Pathology and Dermatology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.
Division of Oral and Maxillofacial Pathology, University of Colorado School of Dental Medicine, Aurora, CO, 80045, USA.

John I Song (JI)

Department of Otolaryngology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

David Raben (D)

Department of Radiation Oncology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

Jill E Slansky (JE)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA.

John H Lee (JH)

Chan Soon-Shiong Institute for Medicine, El Segundo, CA, 90245, USA.

William C Spanos (WC)

Cancer Biology Research Center, Sanford Research, Sioux Falls, SD, 57104, USA.

Dohun Pyeon (D)

Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, 80045, USA. dpyeon@msu.edu.
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI, 48824, USA. dpyeon@msu.edu.

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