Regulation of the master regulator FOXM1 in cancer

被引:304
作者
Liao, Guo-Bin [1 ]
Li, Xin-Zhe [1 ]
Zeng, Shuo [1 ]
Liu, Cheng [1 ]
Yang, Shi-Ming [1 ]
Yang, Li [1 ]
Hu, Chang-Jiang [1 ]
Bai, Jian-Ying [1 ]
机构
[1] Army Med Univ, Xinqiao Hosp, Dept Gastroenterol, Third Mil Med Univ, Chongqing 400037, Peoples R China
来源
CELL COMMUNICATION AND SIGNALING | 2018年 / 16卷
基金
中国国家自然科学基金;
关键词
FOXM1; Regulation; Transcriptional; Post-transcriptional; Post-translational; FORKHEAD BOX M1; TRANSCRIPTION FACTOR FOXM1; POSITIVE FEEDBACK LOOP; EPITHELIAL-MESENCHYMAL TRANSITION; HUMAN HEPATOCELLULAR-CARCINOMA; POTENTIAL PROGNOSTIC MARKER; HUMAN CERVICAL-CANCER; CELL LUNG-CANCER; TARGETING FOXM1; BREAST-CANCER;
D O I
10.1186/s12964-018-0266-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
FOXM1 (forkhead box protein M1) is a critical proliferation-associated transcription factor that is widely spatiotemporally expressed during the cell cycle. It is closely involved with the processes of cell proliferation, self-renewal, and tumorigenesis. In most human cancers, FOXM1 is overexpressed, and this indicates a poor prognosis for cancer patients. FOXM1 maintains cancer hallmarks by regulating the expression of target genes at the transcriptional level. Due to its potential role as molecular target in cancer therapy, FOXM1 was named the Molecule of the Year in 2010. However, the mechanism of FOXM1 dysregulation remains indistinct. A comprehensive understanding of FOXM1 regulation will provide novel insight for cancer and other diseases in which FOXM1 plays a major role. Here, we summarize the transcriptional regulation, post-transcriptional regulation and post-translational modifications of FOXM1, which will provide extremely important implications for novel strategies targeting FOXM1.
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页数:15
相关论文
共 137 条
[1]   Overexpression of FOXM1 Is a Potential Prognostic Marker in Male Breast Cancer [J].
Abdeljaoued, Syrine ;
Bettaieb, Ilhem ;
Nasri, Meher ;
Adouni, Olfa ;
Goucha, Aida ;
El Amine, Olfa ;
Boussen, Hammouda ;
Rahal, Khaled ;
Gamoudi, Amor .
ONCOLOGY RESEARCH AND TREATMENT, 2017, 40 (04) :167-172
[2]   Novel functions of FoxM1: from molecular mechanisms to cancer therapy [J].
Alvarez-Fernandez, Monica ;
Medema, Rene H. .
FRONTIERS IN ONCOLOGY, 2013, 3
[3]   Protein Phosphatase 2A (B55α) Prevents Premature Activation of Forkhead Transcription Factor FoxM1 by Antagonizing Cyclin A/Cyclin-dependent Kinase-mediated Phosphorylation [J].
Alvarez-Fernandez, Monica ;
Halim, Vincentius A. ;
Aprelia, Melinda ;
Mohammed, Shabaz ;
Medema, Rene H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (38) :33029-33036
[4]   A Systematic Screen for CDK4/6 Substrates Links FOXM1 Phosphorylation to Senescence Suppression in Cancer Cells [J].
Anders, Lars ;
Ke, Nan ;
Hydbring, Per ;
Choi, Yoon J. ;
Widlund, Hans R. ;
Chick, Joel M. ;
Zhai, Huili ;
Vidal, Marc ;
Gygi, Stephen P. ;
Braun, Pascal ;
Sicinski, Piotr .
CANCER CELL, 2011, 20 (05) :620-634
[5]   Pro-proliferative FoxM1 is a target of p53-mediated repression [J].
Barsotti, A. M. ;
Prives, C. .
ONCOGENE, 2009, 28 (48) :4295-4305
[6]   Long Noncoding RNAs: Cellular Address Codes in Development and Disease [J].
Batista, Pedro J. ;
Chang, Howard Y. .
CELL, 2013, 152 (06) :1298-1307
[7]   Foxm1 controls a pro-stemness microRNA network in neural stem cells [J].
Besharat, Zein Mersini ;
Abballe, Luana ;
Cicconardi, Francesco ;
Bhutkar, Arjun ;
Grassi, Luigi ;
Le Pera, Loredana ;
Moretti, Marta ;
Chinappi, Mauro ;
D'Andrea, Daniel ;
Mastronuzzi, Angela ;
Ianari, Alessandra ;
Vacca, Alessandra ;
De Smaele, Enrico ;
Locatelli, Franco ;
Po, Agnese ;
Miele, Evelina ;
Ferretti, Elisabetta .
SCIENTIFIC REPORTS, 2018, 8
[8]   Nucleophosmin Interacts with FOXM1 and Modulates the Level and Localization of FOXM1 in Human Cancer Cells [J].
Bhat, Uppoor G. ;
Jagadeeswaran, Ramasamy ;
Halasi, Marianna ;
Gartel, Andrei L. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (48) :41425-41433
[9]   A novel peptide, 9R-P201, strongly inhibits the viability, proliferation and migration of liver cancer HepG2 cells and induces apoptosis by down-regulation of FoxM1 expression [J].
Bi, Zhenfei ;
Liu, Wenrong ;
Ding, Ruofang ;
Wu, Yiran ;
Dou, Rongkun ;
Zhang, Wenwen ;
Yuan, Xue ;
Liu, Xinrong ;
Xiong, Lili ;
Guo, Zhiyun ;
Mao, Canquan .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2017, 796 :175-189
[10]   c-Myc and its target FoxM1 are critical downstream effectors of constitutive androstane receptor (CAR) mediated direct liver hyperplasia [J].
Blanco-Bose, William E. ;
Murphy, Mark J. ;
Ehninger, Armin ;
Offner, Sandra ;
Dubey, Christelle ;
Huang, Wendong ;
Moore, David D. ;
Trumpp, Andreas .
HEPATOLOGY, 2008, 48 (04) :1302-1311