# Loss of DIAPH3 accelerates glioma genesis in mice

## TL;DR

Removing DIAPH3 in mice speeds up the development of brain tumors by causing genetic instability and resistance to radiation.

## Contribution

This study reveals DIAPH3 as a tumor suppressor in glioma development through its role in genome stability and radiation resistance.

## Key findings

- Loss of DIAPH3 and TRP53 leads to earlier tumor formation and increased DNA damage in mice.
- DIAPH3 deficiency causes aneuploidy and genome instability, accelerating glioma progression.
- Glioma stem-like cells lacking DIAPH3 show resistance to ionizing radiation.

## Abstract

DIAPH3 is a master regulator of the cytoskeleton with key roles in cell division. In the mouse brain, DIAPH3-deficient neural stem cells exhibit abnormalities in karyokinesis and cytokinesis, leading to cell cycle arrest, aneuploidy, and mitotic catastrophe. Here, we investigated the role of DIAPH3 in glioma genesis in mouse models. We selectively deleted the Diaph3 and Trp53 genes in the mouse cerebral cortex and thoroughly analyzed single (Diaph3 cKO and Trp53 cKO) and double (dcKO) conditional knockout mice. The tumors appeared earlier in dcKO than in Trp53 cKO mice, and this was associated with increased whole chromosome copy number alterations, endogenous DNA damage, and shorter survival of dcKO mice. We performed a comparative transcriptomic analysis prior to the onset of tumors and identified changes in cancer gene signatures specifically in dcKO, suggesting that the loss of DIAPH3 hastens the tumorigenic process. We isolated cancer stem-like cells and assessed their sensitivity to ionizing radiation and found that DIAPH3 regulates the resistance of glioma stem-like cells to irradiation. Our data suggest that DIAPH3 has a tumor-suppressor function and that its deficiency promotes aneuploidy and genome instability, accelerating tumorigenesis and leading to early onset of high-grade diffuse glioma with DNA damage, and resistance to ionizing radiation.