A lipoprotein-responsive circular RNA, circCTCF, couples extracellular lipid availability to mTOR signaling via ACSL5 in triple-negative breast cancer.

Authors

Yuanyuan Zhang, Zhengyi Liu, Xuanyi Su, Xinyuan Hu, Qing Zhang, Huiyang Zhang, Duan Shicao, Linna Cheng, Xu Dong Zhang, Xiaoying Liu, Song Chen, Rick F Thorne

Published in

International journal of biological macromolecules. Pages 154368. Sep 08, 2026. Epub Sep 08, 2026.

Abstract

Triple-negative breast cancer (TNBC) is an aggressive subtype with limited therapeutic options. While metabolic reprogramming is a hallmark of cancer, most studies have focused on cell-intrinsic alterations in glucose and amino acid metabolism, with comparatively little attention paid to how cancer cells sense and respond to extracellular lipid availability. Here, through an unbiased transcriptomic and circRNA profiling screen under lipoprotein-deprived conditions, we identify circCTCF, a circular RNA derived from the CTCF gene, as a lipoprotein-responsive regulator of lipid metabolism and proliferation in TNBC. circCTCF is significantly downregulated upon lipid withdrawal, and its depletion impairs cell growth while promoting lipid droplet accumulation. Conversely, circCTCF overexpression enhances proliferation and suppresses lipid storage. Mechanistically, circCTCF binds the RNA-binding protein G3BP2 through its back-splice junction sequence to stabilize ACSL5 mRNA, thereby sustaining ACSL5 expression, phosphatidic acid (PA) levels, and mTOR signaling. ACSL5 overexpression rescues PA and mTOR activity in circCTCF-deficient cells, establishing a linear circCTCF-ACSL5-PA-mTOR axis. Furthermore, circCTCF associates with G3BP2-positive stress granules upon heat shock, suggesting a potential link between this metabolic axis and stress-induced RNA regulatory networks. Collectively, these findings establish circCTCF as a critical node coupling extracellular lipid cues to intracellular metabolic control and identify the circCTCF-ACSL5-PA-mTOR axis as a potential therapeutic vulnerability in TNBC.

PMID:
42710763
Bibliographic data and abstract were imported from PubMed on 09 Sep 2026.

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