The NF-κB/ALDH1A1 signaling is established as a key non-genetic mechanism of acquired EGFR-TKI resistance and a rational combination strategy to overcome it is provided.
Abstract
Acquired resistance to tyrosine kinase inhibitors (TKIs) remains a major clinical challenge in the treatment of EGFR-mutant non-small cell lung cancer (NSCLC). This study established TKI-resistant variants by integrating cell lines, lung cancer organoids (LCOs), and in vivo models, revealing the pivotal role of the NF-κB/ALDH1A1 signaling in mediating non-mutational TKI resistance. Resistant cells exhibited elevated RELA phosphorylation, enhanced ALDH1A1 expression and enzymatic activity, and stem-like properties. Mechanistically, NF-κB activation occurred as an early response to TKI exposure and promoted ALDH1A1 transcription via RELA. In turn, ALDH1A1 contributed to the sustained activation of NF-κB signaling, forming a self-reinforcing positive feedback loop. Genetic ALDH1A1 or RELA silencing reversed the resistant phenotype. Pharmacologically, treatment with an EGFR-TKI and the ALDH1A1 inhibitor disulfiram or the NF-κB-targeting agent EGCG synergistically restored the antitumor efficacy of TKIs both in vitro and in vivo. These findings establish the NF-κB/ALDH1A1 signaling as a key non-genetic mechanism of acquired EGFR-TKI resistance and provide a rational combination strategy to overcome it. Catalysis-dependent NF-κB–ALDH1A1 feedback loop drives non-mutational EGFR-TKI resistance. EGFR-TKI treatment suppresses EGFR signaling but rapidly induces NF-κB activation as an early event under TKI stress in EGFR-mutant NSCLC cells. Activated NF-κB (p-RELA) drives ALDH1A1 transcription, while ALDH1A1 enzymatic activity reinforces NF-κB signaling via IKKβ phosphorylation, forming a catalysis-dependent positive feedback loop that sustains stemness and promotes non-mutational TKI resistance. Disruption of this axis by inhibiting ALDH1A1 (DSF) or NF-κB (EGCG) restores TKI sensitivity. Catalysis-dependent NF-κB–ALDH1A1 feedback loop drives non-mutational EGFR-TKI resistance. EGFR-TKI treatment suppresses EGFR signaling but rapidly induces NF-κB activation as an early event under TKI stress in EGFR-mutant NSCLC cells. Activated NF-κB (p-RELA) drives ALDH1A1 transcription, while ALDH1A1 enzymatic activity reinforces NF-κB signaling via IKKβ phosphorylation, forming a catalysis-dependent positive feedback loop that sustains stemness and promotes non-mutational TKI resistance. Disruption of this axis by inhibiting ALDH1A1 (DSF) or NF-κB (EGCG) restores TKI sensitivity.
Findings for the first time identify CLOCK as a critical mediator of EGFR-TKIs resistance and a promising target to overcome EGFR-TKIs resistance in NSCLC.
Yan-Kang Li, Lin-Yu Han, Hui-Wen Luan et al.· Archives of Biochemistry and...· 0 citations
Pharmacologic suppression of IL20RB by APAP presents a novel therapeutic strategy, positioning IL20RB as a promising prognostic biomarker and therapeutic target in NSCLC.
Yang-Hao Wang, Guo-Yun Li, Wei-Zhou Wang et al.· Lung Cancer· 0 citations
A key role is found for NF-κB/Lipocalin 2 (LCN2)-signaling-pathway-induced ferroptosis in modulating cisplatin sensitivity of V600E-overexpressing CRC cells to cisplatin within a KRAS-mutant cellular background, implying LCN2 as a potential therapeutic target.
M. Feng, Xuesong Wu, Li Jiang et al.· Cancers· 0 citations
Target neutralization of SAA1 synergized robustly with osimertinib to reverse immunosuppressive remodeling and induce profound tumor regression in multiple preclinical models, highlighting SAA1 neutralization as a tractable combinatorial strategy to enhance EGFR-TKI efficacy in LUAD.
Jun-Kan Zhu, Shencheng Ren, Tao Cheng et al.· Journal of Experimental &...· 0 citations
IGF1R upregulates PD-L1 via the PI3K/AKT/NF-κB axis through direct NF-κB-mediated transcriptional activation, and PD-L1 serves as a critical downstream effector driving sorafenib resistance in HCC.
Tao Zhu, Chunmei Xie, Qianqian Shao et al.· Molecular Immunology· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.