JAM-A functions as a female microglial tumor suppressor in glioblastoma.


Journal

Neuro-oncology
ISSN: 1523-5866
Titre abrégé: Neuro Oncol
Pays: England
ID NLM: 100887420

Informations de publication

Date de publication:
26 11 2020
Historique:
pubmed: 28 6 2020
medline: 17 3 2021
entrez: 28 6 2020
Statut: ppublish

Résumé

Glioblastoma (GBM) is the most aggressive primary brain tumor and has a dismal prognosis. Previously, we identified that junctional adhesion molecule A (JAM-A), a cell adhesion molecule, is highly elevated in human GBM cancer stem cells and predicts poor patient prognosis. While JAM-A is also highly expressed in other cells in the tumor microenvironment, specifically microglia and macrophages, how JAM-A expression in these cells affects tumor growth has yet to be determined. The goal of this study was to understand the role of microenvironmental JAM-A in mediating GBM growth. Male and female wild-type (WT) and JAM-A-deficient mice were transplanted intracranially with the syngeneic glioma cell lines GL261 and SB28 and were assessed for differences in survival and microglial activation in tumors and in vitro. RNA-sequencing was performed to identify differentially regulated genes among all genotypes, and differences were validated in vitro and in vivo. We found that JAM-A-deficient female mice succumbed to GBM more quickly compared with WT females and JAM-A-deficient and male WT mice. Analysis of microglia in the tumors revealed that female JAM-A-deficient microglia were more activated, and RNA-sequencing identified elevated expression of Fizz1 and Ifi202b specifically in JAM-A-deficient female microglia. Our findings suggest that JAM-A functions to suppress pathogenic microglial activation in the female tumor microenvironment, highlighting an emerging role for sex differences in the GBM microenvironment and suggesting that sex differences extend beyond previously reported tumor cell-intrinsic differences.

Sections du résumé

BACKGROUND
Glioblastoma (GBM) is the most aggressive primary brain tumor and has a dismal prognosis. Previously, we identified that junctional adhesion molecule A (JAM-A), a cell adhesion molecule, is highly elevated in human GBM cancer stem cells and predicts poor patient prognosis. While JAM-A is also highly expressed in other cells in the tumor microenvironment, specifically microglia and macrophages, how JAM-A expression in these cells affects tumor growth has yet to be determined. The goal of this study was to understand the role of microenvironmental JAM-A in mediating GBM growth.
METHODS
Male and female wild-type (WT) and JAM-A-deficient mice were transplanted intracranially with the syngeneic glioma cell lines GL261 and SB28 and were assessed for differences in survival and microglial activation in tumors and in vitro. RNA-sequencing was performed to identify differentially regulated genes among all genotypes, and differences were validated in vitro and in vivo.
RESULTS
We found that JAM-A-deficient female mice succumbed to GBM more quickly compared with WT females and JAM-A-deficient and male WT mice. Analysis of microglia in the tumors revealed that female JAM-A-deficient microglia were more activated, and RNA-sequencing identified elevated expression of Fizz1 and Ifi202b specifically in JAM-A-deficient female microglia.
CONCLUSIONS
Our findings suggest that JAM-A functions to suppress pathogenic microglial activation in the female tumor microenvironment, highlighting an emerging role for sex differences in the GBM microenvironment and suggesting that sex differences extend beyond previously reported tumor cell-intrinsic differences.

Identifiants

pubmed: 32592484
pii: 5864028
doi: 10.1093/neuonc/noaa148
pmc: PMC7690368
doi:

Substances chimiques

Junctional Adhesion Molecule A 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

1591-1601

Subventions

Organisme : NCI NIH HHS
ID : R01 CA213843
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS083629
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA059366
Pays : United States
Organisme : NCI NIH HHS
ID : F32 CA243314
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007250
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS112526
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

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Auteurs

Soumya M Turaga (SM)

Department of Biological, Geological, and Environmental Sciences, Cleveland State University, Cleveland, Ohio.
Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Daniel J Silver (DJ)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio.

Defne Bayik (D)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio.

Evi Paouri (E)

Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Sen Peng (S)

Cancer and Cell Biology Division, TGen, Phoenix, Arizona.

Adam Lauko (A)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Tyler J Alban (TJ)

Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case, Western Reserve University, Cleveland, Ohio.

Nozha Borjini (N)

Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Sarah Stanko (S)

Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.

Ulhas P Naik (UP)

Cardeza Center for Vascular Biology, Department of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania.

Ruth A Keri (RA)

Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio.
Department of Pharmacology and Genetics and Genome Sciences, Case Western Reserve University, Cleveland, Ohio.

James R Connor (JR)

Department of Neurosurgery, Penn State College of Medicine, Hershey, Pennsylvania.

Jill S Barnholtz-Sloan (JS)

Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio.
Department of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio.

Joshua B Rubin (JB)

Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri.

Michael Berens (M)

Cancer and Cell Biology Division, TGen, Phoenix, Arizona.

Dimitrios Davalos (D)

Department of Neurosciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case, Western Reserve University, Cleveland, Ohio.

Justin D Lathia (JD)

Department of Biological, Geological, and Environmental Sciences, Cleveland State University, Cleveland, Ohio.
Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, Ohio.
Department of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case, Western Reserve University, Cleveland, Ohio.
Rose Ella Burkhardt Brain Tumor and Neuro-Oncology Center, Cleveland Clinic, Cleveland, Ohio.

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