FOXO3a and Its Regulators in Prostate Cancer

被引:35
作者
Habrowska-Gorczynska, Dominika Ewa [1 ]
Koziel, Marta Justyna [1 ]
Kowalska, Karolina [1 ]
Piastowska-Ciesielska, Agnieszka Wanda [1 ]
机构
[1] Med Univ Lodz, Dept Cell Cultures & Genom Anal, Zeligowskiego 7-9, PL-90752 Lodz, Poland
关键词
prostate cancer; foxo3a; Akt; proliferation; apoptosis; PROMOTES PROLIFERATION; TRANSCRIPTION FACTORS; APOPTOSIS; EXPRESSION; CELLS; PROGRESSION; METASTASIS; INHIBITION; INDUCTION; REPRESSES;
D O I
10.3390/ijms222212530
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Forkhead box O3 (FOXO3a) is a member of a subfamily of forkhead transcription factors involved in the basic processes within a cell, including proliferation, apoptosis, cell cycle regulation, and DNA damage. As a transcription factor, FOXO3a is involved in the response to cellular stress, UV radiation, or oxidative stress. Its regulation is based on the modification of proteins as well as regulation by other proteins, e.g., growth factors. FOXO3a is commonly deregulated in cancer cells, and its inactivation is associated with initiation and progression of tumorigenesis, suggesting its role as a tumor suppressor; however, its role is still disputed and seems to be dependent on upstream signaling. Nevertheless, FOXO3a serves as an interesting potential target in therapies as it is regulated during treatment with very common anti-cancer drugs such as paclitaxel, cisplatin, docetaxel, and doxorubicin. This review aims to update the reported role of FOXO3a in prostate cancer (PCa), with a focus on its regulators that might serve as potential therapeutic agents in PCa therapy.
引用
收藏
页数:10
相关论文
共 60 条
[1]   Cloning and characterization of three human forkhead genes that comprise an FKHR-like gene subfamily [J].
Anderson, MJ ;
Viars, CS ;
Czekay, S ;
Cavenee, WK ;
Arden, KC .
GENOMICS, 1998, 47 (02) :187-199
[2]   Molecular Basis of Prostate Cancer and Natural Products as Potential Chemotherapeutic and Chemopreventive Agents [J].
Bai, Bingke ;
Chen, Qianbo ;
Jing, Rui ;
He, Xuhui ;
Wang, Hongrui ;
Ban, Yanfei ;
Ye, Qi ;
Xu, Weiheng ;
Zheng, Chengjian .
FRONTIERS IN PHARMACOLOGY, 2021, 12
[3]  
Bao YH, 2017, EUR REV MED PHARMACO, V21, P4548
[4]   MicroRNA-590-3p promotes cell proliferation and invasion by targeting inositol polyphosphate 4-phosphatase type II in human prostate cancer cells [J].
Chen, Haiwen ;
Luo, Qidong ;
Li, Hongliang .
TUMOR BIOLOGY, 2017, 39 (03) :1-8
[5]   Synergistic effect of HIF-1 and FoxO3a trigger cardiomyocyte apoptosis under hyperglycemic ischemia condition [J].
Chen, Ya-Fang ;
Pandey, Sudhir ;
Day, Cecilia Hsuan ;
Chen, Yu-Feng ;
Jiang, Ai-Zhi ;
Ho, Tsung-Jung ;
Chen, Ray-Jade ;
Padma, Vijaya V. ;
Kuo, Wei-Wen ;
Huang, Chih-Yang .
JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (04) :3660-3671
[6]   MicroRNAs and prostate cancer [J].
Coppola, Valeria ;
De Maria, Ruggero ;
Bonci, Desiree .
ENDOCRINE-RELATED CANCER, 2010, 17 (01) :F1-F17
[7]   Glucose-Induced Oxidative Stress Reduces Proliferation in Embryonic Stem Cells via FOXO3A/β-Catenin-Dependent Transcription of p21cip1 [J].
Descalzo, Darcie L. McClelland ;
Satoorian, Tiffany S. ;
Walker, Lauren M. ;
Sparks, Nicole R. L. ;
Pulyanina, Polina Y. ;
zur Nieden, Nicole I. .
STEM CELL REPORTS, 2016, 7 (01) :55-68
[8]   Estrogen receptor β upregulates FOXO3a and causes induction of apoptosis through PUMA in prostate cancer [J].
Dey, P. ;
Stroem, A. ;
Gustafsson, J-A .
ONCOGENE, 2014, 33 (33) :4213-4225
[9]   Effect of MicroRNA-766 Promotes Proliferation, Chemoresistance, Migration, and Invasion of Breast Cancer Cells [J].
Duan, Xiumei ;
Liu, Xiaona ;
Cao, Yuqing ;
Li, Yuxin ;
Silayiding, Aidaeraili ;
Zhang, Li ;
Wang, Jiping .
CLINICAL BREAST CANCER, 2021, 21 (01) :E1-E17
[10]  
European Union©, CANC BURD STAT TREND