Newcastle disease virus exploits Golgi stress and Golgiphagy to promote ferroptosis
: ferrous ions, GA: Golgi apparatus; GOLGA2/GM130: golgin A2; GPX4: glutathione peroxidase 4; GSH: glutathione; GSR: Golgi stress response; HCMV: human cytomegalovirus; HSV-1: herpes simplex virus 1; Lip-1: Liproxstatin-1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MDA: malondialdehyde; mtDNA: mitochondrial DNA; MTOR: mechanistic target of rapamycin kinase; NDV: Newcastle disease virus; NCOA4: nuclear receptor coactivator 4; PUFA: polyunsaturated fatty acid; ROS: reactive oxygen species; Rot: rotenone; SLC7A11: solute carrier family 7 member 11; SERPINH1/HSP47: serpin family H member 1; TFE3: transcription factor binding to IGHM enhancer 3; WT: wild-type.
Authors
- Xianjin Kan
- Guanglei Xie (ORCID: https://orcid.org/0000-0002-5911-004X)
- Chan Ding (ORCID: https://orcid.org/0000-0003-0216-2129)
- Yuan Yu (ORCID: https://orcid.org/0000-0001-5453-2377)
- Yuncong Yin
- Mengqing Yang
- Hui Jiang
Institutions
- Shanghai Jiao Tong University (CN)
- Westlake University (CN)
- Chinese Academy of Agricultural Engineering (CN)
- Yangzhou University (CN)
Publication Details
- Journal
- Autophagy
- Published
- 2026-04-10
- DOI
- https://doi.org/10.1080/15548627.2026.2653010
- Primary Topic
- Ferroptosis and cancer prognosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00