USP13 facilitates a ferroptosis-to-autophagy switch by activation of the NFE2L2/NRF2-SQSTM1/p62-KEAP1 axis dependent on the KRAS signaling pathway

被引:5
作者
Chen, Ling [1 ,2 ,3 ,4 ]
Ning, Jieling [4 ,5 ]
Li, Linghu [1 ,2 ,3 ,4 ]
Tang, Jun [1 ,2 ,3 ,4 ]
Liu, Na [6 ,7 ]
Long, Yao [1 ,2 ,3 ,4 ]
Sun, Jingyue [1 ,2 ,3 ,4 ]
Lv, Cairui [1 ,2 ,3 ,4 ]
Shi, Ying [1 ,2 ,3 ,4 ]
Tao, Tania [1 ,2 ,3 ,4 ]
Xiao, Desheng [3 ,8 ]
Cao, Ya [4 ]
Wang, Xiang [9 ]
Liu, Shuang [10 ]
Li, Guangjian [11 ]
Zhang, Bin [5 ]
Tao, Yongguang [1 ,2 ,3 ,4 ,8 ,9 ]
机构
[1] Cent South Univ, Hunan Canc Hosp, Hunan Key Lab Canc Metab, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Affiliated Canc Hosp, Xiangya Sch Med, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Dept Pathol, 87 Xiangya Rd, Changsha 410008, Hunan, Peoples R China
[4] Cent South Univ, Canc Res Inst, NHC Key Lab Carcinogenesis, Key Lab Carcinogenesis & Canc Invas,Minist Educ, Changsha, Hunan, Peoples R China
[5] Cent South Univ, Sch Basic Med, Dept Histol & Embryol, 172 Tongzipo Rd, Changsha 410013, Peoples R China
[6] Cent South Univ, Xiangya Hosp, Dept Neurosurg, Postdoctoral Res Workstat, Changsha, Chin, Myanmar
[7] Cent South Univ, Xiangya Hosp, Hunan Int Sci & Technol Cooperat Base Brain Tumor, Changsha, Hunan, Peoples R China
[8] Cent South Univ, Sch Basic Med, Dept Pathol, Changsha, Peoples R China
[9] Cent South Univ, Xiangya Hosp 2, Dept Thorac Surg, Hunan Key Lab Early Diag & Precis Therapy Lung Can, Changsha, Hunan, Peoples R China
[10] Cent South Univ, Natl Clin Res Ctr Geriatr Disorders, Dept Oncol,Inst Med Sci, Changsha, Hunan, Peoples R China
[11] Kunming Med Univ, Affiliated Hosp 3, Yunnan Canc Hosp, Dept Thorac Surg 1, Kunming, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Autophagy; ferroptosis; LUAD; SQSTM1; USP13; TRANSCRIPTION FACTOR NRF2; OXIDATIVE STRESS; SELECTIVE AUTOPHAGY; PROTEIN; DEGRADATION; P62/SQSTM1; REDOX; RAS; EXPRESSION; MECHANISM;
D O I
10.1080/15548627.2024.2410619
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macroautophagy/autophagyis a lysosomal-regulated degradation process that participates incellular stress and then promotes cell survival or triggers celldeath. Ferroptosis was initially described as anautophagy-independent, iron-regulated, nonapoptotic cell death.However, recent studies have revealed that autophagy is positivelyassociated with sensitivity to ferroptosis. Nonetheless, themolecular mechanisms by which these two types of regulated cell death(RCD) modulate each other remain largely unclear. Here, we screened85 deubiquitinating enzymes (DUBs) and found that overexpression ofUSP13 (ubiquitin specific peptidase 13) could significantlyupregulate NFE2L2/NRF2 (NFE2 like bZIP transcription factor 2)protein levels. In addition, in 39 cases of KRAS-mutated lungadenocarcinoma (LUAD), we found that approximately 76% of USP13overexpression is positively correlated with NFE2L2 overexpression.USP13 interacts with and catalyzes the deubiquitination of thetranscription factor NFE2L2. Additionally, USP13 depletion promotesan autophagy-to-ferroptosis switch invitro andin xenograft tumor mouse models, through the activation of theNFE2L2-SQSTM1/p62 (sequestosome 1)-KEAP1 axis in KRAS mutant cellsand tumor tissues. Hence, targeting USP13 effectively switchedautophagy-to-ferroptosis, thereby inhibiting KRAS (KRASproto-oncogene, GTPase) mutant LUAD, suggesting the therapeuticpromise of combining autophagy and ferroptosis in the KRAS-mutantLUAD.Abbreviation: ACSL4: acyl-CoA synthetase long-chain family member 4; ACTB: actin beta; AL: autolysosomes; AP: autophagosomes; BCL2L1/BCL-xL: BCL2 like 1; CCK8: Cell Counting Kit-8; CQ: chloroquine; CUL3: cullin 3; DMSO: dimethyl sulfoxide; DOX: doxorubicin; DUB: deubiquitinating enzyme; Ferr-1: ferrostatin-1; GPX4: glutathione peroxidase 4; GSEA: gene set enrichment analysis; 4HNE: 4-hydroxynonenal; IKE: imidazole ketone erastin; KEAP1: kelch like ECH associated protein 1; KRAS: KRAS proto-oncogene, GTPase; LCSC: lung squamous cell carcinoma; IF: immunofluorescence; LUAD: lung adenocarcinoma; Lys05: Lys01 trihydrochloride; MAPK1/ERK2/p42: mitogen-activated protein kinase 1; MAPK3/ERK1/p44; MTOR: mechanistic target of rapamycin kinase; NFE2L2/NRF2: NFE2 like bZIP transcription factor, 2; NQO1: NAD(P)H quinone dehydrogenase 1; PG: phagophore; RCD: regulated cell death; RAPA: rapamycin; ROS: reactive oxygen species; SLC7A11/xCT: solute carrier family 7 member 11; SQSTM1/p62: sequestosome 1; TEM: transmission electron microscopy; TUBB/beta-tubulin: tubulin, beta; UPS: ubiquitin-proteasome system; USP13: ubiquitin specific peptidase 13.
引用
收藏
页码:565 / 582
页数:18
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