Oncogenic role of FOXM1 in human prostate cancer (Review)

被引:2
作者
Lee, Da Young [1 ]
Chun, Jung Nyeo [1 ,2 ]
So, Insuk [1 ,2 ]
Jeon, Ju-Hong [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Physiol & Biomed Sci, Coll Med, 103 Daehak Ro, Seoul 03080, South Korea
[2] Seoul Natl Univ, Inst Human Environm Interface Biol, Seoul 03080, South Korea
基金
新加坡国家研究基金会;
关键词
FOXM1; prostate cancer; oncogene; FORKHEAD BOX M1; EXPRESSION; TRANSCRIPTION; PROGRESSION; INHIBITION; STATISTICS; TRAMP;
D O I
10.3892/or.2023.8674
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is the leading cause of cancer-related mortality among men worldwide. In particular, castration-resistant prostate cancer presents a formidable clinical challenge and emphasizes the need to develop novel therapeutic strategies. Forkhead box M1 (FOXM1) is a multifaceted transcription factor that is implicated in the acquisition of the multiple cancer hallmark capabilities in prostate cancer cells, including sustaining proliferative signaling, resisting cell death and the activation of invasion and metastasis. Elevated FOXM1 expression is frequently observed in prostate cancer, and in particular, FOXM1 overexpression is closely associated with poor clinical outcomes in patients with prostate cancer. In the present review, recent advances in the understanding of the oncogenic role of deregulated FOXM1 expression in prostate cancer were highlighted. In addition, the molecular mechanisms by which FOXM1 regulates prostate cancer development and progression were described, thereby providing knowledge and a conceptual framework for FOXM1. The present review also provided valuable insight into the inherent challenges associated with translating biomedical knowledge into effective therapeutic strategies for prostate cancer.
引用
收藏
页数:9
相关论文
共 62 条
[1]   Cross-Species Regulatory Network Analysis Identifies a Synergistic Interaction between FOXM1 and CENPF that Drives Prostate Cancer Malignancy [J].
Aytes, Alvaro ;
Mitrofanova, Antonina ;
Lefebvre, Celine ;
Alvarez, Mariano J. ;
Castillo-Martin, Mireia ;
Zheng, Tian ;
Eastham, James A. ;
Gopalan, Anuradha ;
Pienta, Kenneth J. ;
Shen, Michael M. ;
Califano, Andrea ;
Abate-Shen, Cory .
CANCER CELL, 2014, 25 (05) :638-651
[2]   Underlying Features of Prostate Cancer-Statistics, Risk Factors, and Emerging Methods for Its Diagnosis [J].
Berenguer, Cristina V. V. ;
Pereira, Ferdinando ;
Camara, Jose S. ;
Pereira, Jorge A. M. .
CURRENT ONCOLOGY, 2023, 30 (02) :2300-2321
[3]   In silico, in vitro and in vivo studies: Dibutyl phthalate promotes prostate cancer cell proliferation by activating Forkhead Box M1 and remission after Natura-α pretreatment [J].
Bu, Hengtao ;
Tang, Sensheng ;
Liu, Guiting ;
Miao, Chenkui ;
Zhou, Xiang ;
Yang, Haiwei ;
Liu, Bianjiang .
TOXICOLOGY, 2023, 488
[4]   Current therapy and drug resistance in metastatic castration-resistant prostate cancer [J].
Cai, Maoping ;
Song, Xian-Lu ;
Li, Xin-An ;
Chen, Mingkun ;
Guo, Jiading ;
Yang, Dong Hua ;
Chen, Zhanghui ;
Zhao, Shan-Chao .
DRUG RESISTANCE UPDATES, 2023, 68
[5]   Foxm1 Expression in Prostate Epithelial Cells Is Essential for Prostate Carcinogenesis [J].
Cai, Yuqi ;
Balli, David ;
Ustiyan, Vladimir ;
Fulford, Logan ;
Hiller, Andrea ;
Misetic, Vinko ;
Zhang, Yufang ;
Paluch, Andrew M. ;
Waltz, Susan E. ;
Kasper, Susan ;
Kalin, Tanya V. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (31) :22527-22541
[6]   Forkhead Box Transcription Factors: Double-Edged Swords in Cancer [J].
Castaneda, Maria ;
den Hollander, Petra ;
Mani, Sendurai A. .
CANCER RESEARCH, 2022, 82 (11) :2057-2065
[7]   Gene expression profiles of prostate cancer reveal involvement of multiple molecular pathways in the metastatic process [J].
Chandran, Uma R. ;
Ma, Changqing ;
Dhir, Rajiv ;
Bisceglia, Michelle ;
Lyons-Weiler, Maureen ;
Liang, Wenjing ;
Michalopoulos, George ;
Becich, Michael ;
Monzon, Federico A. .
BMC CANCER, 2007, 7 (1)
[8]   SPDEF Inhibits Prostate Carcinogenesis by Disrupting a Positive Feedback Loop in Regulation of the Foxm1 Oncogene [J].
Cheng, Xin-Hua ;
Black, Markaisa ;
Ustiyan, Vladimir ;
Le, Tien ;
Fulford, Logan ;
Sridharan, Anusha ;
Medvedovic, Mario ;
Kalinichenko, Vladimir V. ;
Whitsett, Jeffrey A. ;
Kalin, Tanya V. .
PLOS GENETICS, 2014, 10 (09)
[9]   FOXM1 in Cancer: Interactions and Vulnerabilities [J].
Gartel, Andrei L. .
CANCER RESEARCH, 2017, 77 (12) :3135-3139
[10]   Aromatic monophenols from cinnamon bark act as proteasome inhibitors by upregulating ER stress, suppressing FoxM1 expression, and inducing apoptosis in prostate cancer cells [J].
Gopalakrishnan, Srividya ;
Ismail, Ayesha .
PHYTOTHERAPY RESEARCH, 2021, 35 (10) :5781-5794