Author ORCID Identifier

Maria F. Gonzalez-Aponte: 0000-0002-8139-312X

Yotong Huang: 0000-0002-5200-8077

William A. Leidig: 0009-0008-3127-3905

Tatiana Simon: 0000-0001-5686-8798

Omar H. Butt: 0000-0003-2252-3673

Marc D. Ruben: 0000-0002-7893-0238

Albert H. Kim: 0000-0002-1751-8493

Joshua B. Rubin: 0000-0002-7395-1937

Erik D. Herzog: 0000-0001-7209-5174

Olivia J. Walch: 0000-0002-7881-6910

Document Type

Article

Publication Date

2025

Publication Title

Journal of Neuro-Oncology

Abstract

Purpose Recent studies show that glioblastoma (GBM) is more sensitive to temozolomide (TMZ) in the morning. In cells, inhibiting O6-Methylguanine-DNA-Methyltransferase (MGMT) abolished time-dependent TMZ efficacy, suggesting that circadian regulation of this DNA repair enzyme underlies daily TMZ sensitivity. Here, we tested the hypotheses that MGMT promoter methylation and protein abundance vary with time-of-day in GBM, resulting in daily rhythms in TMZ efficacy.

Methods We assessed daily rhythms in MGMT promoter methylation in GBM in vitro and retrospectively analyzed MGMT methylation status in human GBM biopsies collected at different times of day. Next, we measured MGMT and BMAL1 protein abundances in GBM cells collected at four-hour intervals. To understand the therapeutic implications of circadian variations in MGMT, we incorporated its daily rhythms into an in vitro mathematical model capturing interactions between MGMT, TMZ, and GBM DNA.

Results We found daily rhythms in MGMT promoter methylation and protein levels in GBM in vitro, and in patient biopsies peaking at midday. Further, MGMT protein levels peaked at CT4, corresponding to the time of maximal TMZ efficacy in vitro. When we incorporated cell-intrinsic circadian rhythms in MGMT protein into a mathematical model for GBM chemotherapy, we found that dosing when daily MGMT levels peaked and began to decline produced maximum DNA damage.

Conclusion Our findings suggest that the likelihood of diagnosis of MGMT promoter methylation may vary with time of biopsy in GBM. Furthermore, theoretical modeling predicts that efforts to deliver TMZ after the daily peak of MGMT activity, with exact time being dose-dependent, may significantly enhance its therapeutic efficacy.

Keywords

GBM, TMZ, MGMT, expression and promoter methylation, Chronotherapy, Chronodiagnosis

Volume

176

Issue

36

DOI

https://doi.org/10.1007/s11060-025-05242-3

Rights

© The Author(s) 2025

Version

Version of Record

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