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

Soumya M. Turaga, Daniel J. Silver, Defne Bayik, Evi Paouri, Sen Peng, Adam Lauko, Tyler J. Alban, Nozha Borjini, Sarah Stanko, Ulhas P. Naik, Ruth A. Keri, James R. Connor, Jill S. Barnholtz-Sloan, Joshua B. Rubin, Michael Berens, Dimitrios Davalos, Justin D. Lathia

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)1591-1601
Number of pages11
JournalNeuro-oncology
Volume22
Issue number11
DOIs
StatePublished - Nov 1 2020

All Science Journal Classification (ASJC) codes

  • Oncology
  • Clinical Neurology
  • Cancer Research

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