Human Endogenous Retrovirus Type K Promotes Proliferation and Confers Sensitivity to Antiretroviral Drugs in Merlin-Negative Schwannoma and Meningioma.


Journal

Cancer research
ISSN: 1538-7445
Titre abrégé: Cancer Res
Pays: United States
ID NLM: 2984705R

Informations de publication

Date de publication:
15 01 2022
Historique:
received: 20 11 2020
revised: 04 03 2021
accepted: 15 11 2021
pubmed: 3 12 2021
medline: 19 2 2022
entrez: 2 12 2021
Statut: ppublish

Résumé

Deficiency of the tumor suppressor Merlin causes development of schwannoma, meningioma, and ependymoma tumors, which can occur spontaneously or in the hereditary disease neurofibromatosis type 2 (NF2). Merlin mutations are also relevant in a variety of other tumors. Surgery and radiotherapy are current first-line treatments; however, tumors frequently recur with limited treatment options. Here, we use human Merlin-negative schwannoma and meningioma primary cells to investigate the involvement of the endogenous retrovirus HERV-K in tumor development. HERV-K proteins previously implicated in tumorigenesis were overexpressed in schwannoma and all meningioma grades, and disease-associated CRL4

Identifiants

pubmed: 34853069
pii: 0008-5472.CAN-20-3857
doi: 10.1158/0008-5472.CAN-20-3857
doi:

Substances chimiques

Anti-Retroviral Agents 0
NF2 protein, human 0
Neurofibromin 2 0
Viral Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

235-247

Subventions

Organisme : Medical Research Council
ID : G0701018
Pays : United Kingdom
Organisme : Medical Research Council
ID : G1100578
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/N004272/1
Pays : United Kingdom

Informations de copyright

©2021 American Association for Cancer Research.

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Auteurs

Emmanuel A Maze (EA)

School of Biomedical Sciences, Faculty of Health: Medicine, Dentistry and Human Sciences, University of Plymouth, Plymouth, United Kingdom.

Bora Agit (B)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

Shona Reeves (S)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

David A Hilton (DA)

Department of Cellular and Anatomical Pathology, University Hospitals Plymouth NHS Trust, Derriford, Plymouth, Devon, United Kingdom.

David B Parkinson (DB)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

Liyam Laraba (L)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

Emanuela Ercolano (E)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

Kathreena M Kurian (KM)

Department of Neuropathology, Brain Tumour Research Group, Frenchay Hospital, University of Bristol, Bristol, United Kingdom.

C Oliver Hanemann (CO)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom.

Robert D Belshaw (RD)

School of Biomedical Sciences, Faculty of Health: Medicine, Dentistry and Human Sciences, University of Plymouth, Plymouth, United Kingdom. sylwia.ammoun@plymouth.ac.uk rbelshaw@kean.edu.
Department of Biology, College of Science and Technology, Wenzhou-Kean University, Wenzhou, Zhejiang Province, China.

Sylwia Ammoun (S)

Peninsula Medical School, Faculty of Health: Medicine, Dentistry and Human Sciences, Plymouth University, Plymouth, United Kingdom. sylwia.ammoun@plymouth.ac.uk rbelshaw@kean.edu.

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