The role of TXNIP in cancer: a fine balance between redox, metabolic, and immunological tumor control

被引:18
作者
Deng, Jinhai [1 ,2 ]
Pan, Teng [3 ]
Liu, Zaoqu [4 ]
McCarthy, Caitlin [1 ]
Vicencio, Jose M. [1 ]
Cao, Lulu [5 ,6 ]
Alfano, Giovanna [1 ]
Suwaidan, Ali Abdulnabi [1 ]
Yin, Mingzhu [2 ]
Beatson, Richard [1 ,7 ]
Ng, Tony [1 ,8 ,9 ]
机构
[1] Kings Coll London, Sch Canc & Pharmaceut Sci, Richard Dimbleby Lab Canc Res, London, England
[2] Chongqing Univ, Clin Res Ctr CRC, Clin Pathol Ctr CPC, Three Gorges Hosp, Chongqing, Peoples R China
[3] Shantou Univ, Longgang Dist Matern & Child Healthcare Hosp Shenz, Longgang Matern & Child Inst, Med Coll, Shenzhen 518172, Peoples R China
[4] Zhengzhou Univ, Dept Intervent Radiol, Affiliated Hosp 1, Zhengzhou, Peoples R China
[5] Peking Univ Peoples Hosp, Dept Rheumatol & Immunol, Beijing, Peoples R China
[6] Beijing Key Lab Rheumatism Mech & Immune Diag BZ01, Beijing, Peoples R China
[7] Univ Coll London UCL, Ctr Inflammat & Tissue Repair, Div Med, UCL Resp, Rayne 9 Bldg, London WC1E 6JF, England
[8] UCL, UCL Canc Inst, London, England
[9] Canc Res UK City London Ctr, London, England
关键词
THIOREDOXIN-INTERACTING-PROTEIN; UP-REGULATED PROTEIN-1; GENE-EXPRESSION; OXIDATIVE STRESS; D-ALLOSE; HEPATOCELLULAR-CARCINOMA; LUNG ADENOCARCINOMA; NLRP3; INFLAMMASOME; DENDRITIC CELLS; SMALL-MOLECULE;
D O I
10.1038/s41416-023-02442-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thioredoxin-interacting protein (TXNIP) is commonly considered a master regulator of cellular oxidation, regulating the expression and function of Thioredoxin (Trx). Recent work has identified that TXNIP has a far wider range of additional roles: from regulating glucose and lipid metabolism, to cell cycle arrest and inflammation. Its expression is increased by stressors commonly found in neoplastic cells and the wider tumor microenvironment (TME), and, as such, TXNIP has been extensively studied in cancers. In this review, we evaluate the current literature regarding the regulation and the function of TXNIP, highlighting its emerging role in modulating signaling between different cell types within the TME. We then assess current and future translational opportunities and the associated challenges in this area. An improved understanding of the functions and mechanisms of TXNIP in cancers may enhance its suitability as a therapeutic target.
引用
收藏
页码:1877 / 1892
页数:16
相关论文
共 229 条
[1]   Alternative Splicing and Cleavage of GLUT8 [J].
Alexander, Caroline M. ;
Martin, Joshua A. ;
Oxman, Elias ;
Kasza, Ildiko ;
Senn, Katherine A. ;
Dvinge, Heidi .
MOLECULAR AND CELLULAR BIOLOGY, 2021, 41 (01)
[2]   TXNIP in Metabolic Regulation: Physiological Role and Therapeutic Outlook [J].
Alhawiti, Naif Mohammad ;
Al Mahri, Saeed ;
Aziz, Mohammad Azhar ;
Malik, Shuja Shafi ;
Mohammad, Sameer .
CURRENT DRUG TARGETS, 2017, 18 (09) :1095-1103
[3]   TXNIP Switches Tracks toward a Terminal UPR [J].
Anthony, Tracy G. ;
Wek, Ronald C. .
CELL METABOLISM, 2012, 16 (02) :135-137
[4]   Endoplasmic reticulum stress signaling and chemotherapy resistance in solid cancers [J].
Avril, T. ;
Vauleron, E. ;
Chevet, E. .
ONCOGENESIS, 2017, 6 :e373-e373
[5]   Identification of thioredoxin-interacting protein 1 as a hypoxia-inducible factor 1α-induced gene in pancreatic cancer [J].
Baker, Amanda F. ;
Koh, Mei Y. ;
Williams, Ryan R. ;
James, Brian ;
Wang, Huamin ;
Tate, Wendy R. ;
Gallegos, Alfred ;
Von Hoff, Daniel D. ;
Han, Haiyong ;
Powis, Garth .
PANCREAS, 2008, 36 (02) :178-186
[6]   BCL6: Master Regulator of the Germinal Center Reaction and Key Oncogene in B Cell Lymphomagenesis [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
ADVANCES IN IMMUNOLOGY, VOL 105, 2010, 105 :193-210
[7]   Pancreatic cancers suppress negative feedback of glucose transport to reprogram chromatin for metastasis [J].
Bechard, Matthew E. ;
Smalling, Rana ;
Hayashi, Akimasa ;
Zhong, Yi ;
Word, Anna E. ;
Campbell, Sydney L. ;
Tran, Amanda V. ;
Weiss, Vivian L. ;
Iacobuzio-Donahue, Christine ;
Wellen, Kathryn E. ;
McDonald, Oliver G. .
NATURE COMMUNICATIONS, 2020, 11 (01)
[8]  
Boyer S, 2022, ELIFE, V11, DOI [10.7554/eLife.73796, 10.7554/eLife.73796.sa0, 10.7554/eLife.73796.sa1, 10.7554/eLife.73796.sa2]
[9]   Long non-coding RNA Gm15441 attenuates hepatic inflammasome activation in response to PPARA agonism and fasting [J].
Brocker, Chad N. ;
Kim, Donghwan ;
Melia, Tisha ;
Karri, Kritika ;
Velenosi, Thomas J. ;
Takahashi, Shogo ;
Aibara, Daisuke ;
Bonzo, Jessica A. ;
Levi, Moshe ;
Waxman, David J. ;
Gonzalez, Frank J. .
NATURE COMMUNICATIONS, 2020, 11 (01)
[10]   Endoplasmic Reticulum Stress Activates the Inflammasome via NLRP3-and Caspase-2-Driven Mitochondrial Damage [J].
Bronner, Denise N. ;
Abuaita, Basel H. ;
Chen, Xiaoyun ;
Fitzgerald, Katherine A. ;
Nunez, Gabriel ;
He, Yongqun ;
Yin, Xiao-Ming ;
O'Riordan, Mary X. D. .
IMMUNITY, 2015, 43 (03) :451-462