8HZ8

Structure of PPIA in complex with the peptide of NRF2

8HZ8 の概要

• エントリーDOI: 10.2210/pdb8hz8/pdb
• 分子名称: Peptidyl-prolyl cis-trans isomerase A, N-terminally processed, NRF2 peptide (3 entities in total)
• 機能のキーワード: molrcular chperone, isomerase
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 18289.78

構造登録者

Wanyan, W.,Hui, M.,Jin, H.,Lu, W. (登録日: 2023-01-08, 公開日: 2024-03-13, 最終更新日: 2024-10-30)

主引用文献

Lu, W.,Cui, J.,Wang, W.,Hu, Q.,Xue, Y.,Liu, X.,Gong, T.,Lu, Y.,Ma, H.,Yang, X.,Feng, B.,Wang, Q.,Zhang, N.,Xu, Y.,Liu, M.,Nussinov, R.,Cheng, F.,Ji, H.,Huang, J.
PPIA dictates NRF2 stability to promote lung cancer progression.
Nat Commun, 15:4703-4703, 2024

PubMed Abstract: Nuclear factor erythroid 2-related factor 2 (NRF2) hyperactivation has been established as an oncogenic driver in a variety of human cancers, including non-small cell lung cancer (NSCLC). However, despite massive efforts, no specific therapy is currently available to target NRF2 hyperactivation. Here, we identify peptidylprolyl isomerase A (PPIA) is required for NRF2 protein stability. Ablation of PPIA promotes NRF2 protein degradation and blocks NRF2-driven growth in NSCLC cells. Mechanistically, PPIA physically binds to NRF2 and blocks the access of ubiquitin/Kelch Like ECH Associated Protein 1 (KEAP1) to NRF2, thus preventing ubiquitin-mediated degradation. Our X-ray co-crystal structure reveals that PPIA directly interacts with a NRF2 interdomain linker via a trans-proline 174-harboring hydrophobic sequence. We further demonstrate that an FDA-approved drug, cyclosporin A (CsA), impairs the interaction of NRF2 with PPIA, inducing NRF2 ubiquitination and degradation. Interestingly, CsA interrupts glutamine metabolism mediated by the NRF2/KLF5/SLC1A5 pathway, consequently suppressing the growth of NRF2-hyperactivated NSCLC cells. CsA and a glutaminase inhibitor combination therapy significantly retard tumor progression in NSCLC patient-derived xenograft (PDX) models with NRF2 hyperactivation. Our study demonstrates that targeting NRF2 protein stability is an actionable therapeutic approach to treat NRF2-hyperactivated NSCLC.

PubMed: 38830868
DOI: 10.1038/s41467-024-48364-4

実験手法

X-RAY DIFFRACTION (1.81 Å)