HOX genes and the NF-κB pathway: A convergence of developmental biology, inflammation and cancer biology

被引:54
作者
Pai, Priya [1 ]
Sukumar, Saraswati [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21231 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2020年 / 1874卷 / 02期
关键词
HOX; NF-KB; Inflammation; Cancer; Homeostasis; POLYCOMB TARGET GENES; BREAST-CANCER; TRANSCRIPTION FACTORS; MOLECULAR PATHWAYS; NEGATIVE REGULATOR; SUPPRESSOR-CELLS; EXPRESSION; GROWTH; ALPHA; ACTIVATION;
D O I
10.1016/j.bbcan.2020.188450
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
The roles of HOX transcription factors as oncogenes and tumor suppressor genes, and the NF-KB pathway in chronic inflammation, both leading to cancer are well-established. HOX transcription factors are members of an evolutionarily conserved family of proteins required for anteroposterior body axis patterning during embryonic development, and are often dysregulated in cancer. The NF-KB pathway aids inflammation and immunity but it is also important during embryonic development. It is frequently activated in both solid and hematological malignancies. NF-KB and HOX proteins can influence each other through mutual transcriptional regulation, protein-protein interactions, and regulation of upstream and downstream interactors. These interactions have important implications both in homeostasis and in disease. In this review, we summarize the role of HOX proteins in regulating inflammation in homeostasis and disease- with a particular emphasis on cancer. We also describe the relationship between HOX genes and the NF-KB pathway, and discuss potential therapeutic strategies.
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页数:11
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共 161 条
[21]   HOXA5 acts directly downstream of retinoic acid receptor β and contributes to retinoic acid-induced apoptosis and growth inhibition [J].
Chen, Hexin ;
Zhang, Huiping ;
Lee, Jishin ;
Liang, Xiaohui ;
Wu, Xinyan ;
Zhu, Tao ;
Lo, Pang-kuo ;
Zhang, Xiaokun ;
Sukumar, Saraswati .
CANCER RESEARCH, 2007, 67 (17) :8007-8013
[22]   Identification of transcriptional targets of HOXA5 [J].
Chen, HX ;
Rubin, E ;
Zhang, HP ;
Chung, S ;
Jie, CC ;
Garrett, E ;
Biswal, S ;
Sukumar, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (19) :19373-19380
[23]   HOXA5-induced apoptosis in breast cancer cells is mediated by caspases 2 and 8 [J].
Chen, HX ;
Chung, S ;
Sukumar, S .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (02) :924-935
[24]   Molecular Pathways: VCAM-1 as a Potential Therapeutic Target in Metastasis [J].
Chen, Qing ;
Massague, Joan .
CLINICAL CANCER RESEARCH, 2012, 18 (20) :5520-5525
[25]   Role of HOXA9 in leukemia: dysregulation, cofactors and essential targets [J].
Collins, C. T. ;
Hess, J. L. .
ONCOGENE, 2016, 35 (09) :1090-1098
[26]   The homeotic protein HOXC13 is a member of human DNA replication complexes [J].
Comelli, Laura ;
Marchetti, Laura ;
Arosio, Daniele ;
Riva, Silvano ;
Abdurashidova, Gulnara ;
Beltram, Fabio ;
Falaschi, Arturo .
CELL CYCLE, 2009, 8 (03) :454-459
[27]   A Hox Code Defines Spinocerebellar Neuron Subtype Regionalization [J].
Coughlan, Eamon ;
Garside, Victoria C. ;
Wong, Siew Fen Lisa ;
Liang, Huazheng ;
Kraus, Dominik ;
Karmakar, Kajari ;
Maheshwari, Upasana ;
Rijli, Filippo M. ;
Bourne, James ;
McGlinn, Edwina .
CELL REPORTS, 2019, 29 (08) :2408-+
[28]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[29]   Sustained Endothelial Expression of HoxA5 In Vivo Impairs Pathological Angiogenesis And Tumor Progression [J].
Cuevas, Ileana ;
Layman, Hans ;
Coussens, Lisa ;
Boudreau, Nancy .
PLOS ONE, 2015, 10 (03)
[30]   The MicroRNA hsa-let-7g Promotes Proliferation and Inhibits Apoptosis in Lung Cancer by Targeting HOXB1 [J].
Cui, Fenghe ;
Zhou, Qian ;
Xiao, Kuang ;
Ma, Shengwei .
YONSEI MEDICAL JOURNAL, 2020, 61 (03) :210-217