Lactate-Induced Lactylation Enhances BMAL1 Transcription and Nuclear Translocation, Promoting Bevacizumab Resistance in Glioblastoma through VEGFA

View at publisher
Authors: Fan Wang, Wenjun Liao, Caiyan Li, Rui Duan, Lvan Chen
Cited by: 1
References: 48

Abstract

PURPOSE: Resistance to bevacizumab (Bev) remains a major challenge in the management of glioblastoma multiforme (GBM). Our previous work indicated that brain and muscle ARNT-like 1 (BMAL1) participates in lactate metabolism in GBM and may be involved in the mechanisms underlying Bev resistance. However, the specific roles of BMAL1 and lactate in this process require further investigation. EXPERIMENTAL DESIGN: This study employed a comprehensive strategy combining in vitro GBM cell line models, patient-derived xenografts (PDX), and in vivo mouse studies. Functional assays (Cell Counting Kit-8 and 3D spheroid invasion), molecular techniques [chromatin immunoprecipitation-quantitative polymerase chain reaction, coimmunoprecipitation, and immunoprecipitation and mass spectrometry (IP-MS)], and biochemical analyses were performed to dissect the mechanism. The clinical relevance of our findings was validated in five independent GBM cohorts and through the analysis of human GBM tissues. RESULTS: We identified a previously unrecognized signaling axis in which lactate promotes BMAL1 expression via H3K18la modification at its promoter. In addition, lactate induces BMAL1 protein lactylation at lysine 123, which facilitates its nuclear translocation. IP-MS further showed that lactylated BMAL1 displays a strengthened interaction with tubulin alpha 1c (TUBA1C), a protein essential for its nuclear import. This lactylation-dependent BMAL1/TUBA1C complex subsequently enhances vascular endothelial growth factor A (VEGFA) transcription, thereby driving Bev resistance. Importantly, targeting this pathway either by silencing BMAL1, inhibiting lactate transporters, or introducing a lactylation-deficient BMAL1-K123 mutant effectively restored Bev sensitivity in vitro and in vivo. CONCLUSIONS: These findings reveal a novel mechanism through which lactate-mediated lactylation of BMAL1 promotes Bev resistance in GBM, supporting the lactate/BMAL1/TUBA1C/VEGFA axis as a promising therapeutic target for overcoming Bev resistance in patients with GBM.

Fields of Study & Subjects

Glioma Diagnosis and Treatment Cancer Hypoxia and Metabolism Histone Deacetylase Inhibitors Research

Publication details

Journal / source
Clinical Cancer Research
Publisher
American Association for Cancer Research (AACR)
Volume
32
Issue
15
Pages
3395–3409
Publication date
17 April 2026
Language
EN