Protein kinase CK2: a potential therapeutic target for diverse human diseases

被引:227
作者
Borgo, Christian [1 ]
D'Amore, Claudio [1 ]
Sarno, Stefania [1 ]
Salvi, Mauro [1 ]
Ruzzene, Maria [1 ,2 ]
机构
[1] Univ Padua, Dept Biomed Sci, Padua, Italy
[2] Univ Padua, Inst Neurosci, CNR, Padua, Italy
关键词
NF-KAPPA-B; ALPHA-SYNUCLEIN PHOSPHORYLATION; UNFAVORABLE PROGNOSTIC MARKER; LYMPHOBLASTIC-LEUKEMIA CELLS; CK2-ALPHA CATALYTIC SUBUNIT; STRUCTURE-BASED DESIGN; 2 INHIBITOR CX-4945; CASEIN KINASE; UP-REGULATION; GENE-EXPRESSION;
D O I
10.1038/s41392-021-00567-7
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
CK2 is a constitutively active Ser/Thr protein kinase, which phosphorylates hundreds of substrates, controls several signaling pathways, and is implicated in a plethora of human diseases. Its best documented role is in cancer, where it regulates practically all malignant hallmarks. Other well-known functions of CK2 are in human infections; in particular, several viruses exploit host cell CK2 for their life cycle. Very recently, also SARS-CoV-2, the virus responsible for the COVID-19 pandemic, has been found to enhance CK2 activity and to induce the phosphorylation of several CK2 substrates (either viral and host proteins). CK2 is also considered an emerging target for neurological diseases, inflammation and autoimmune disorders, diverse ophthalmic pathologies, diabetes, and obesity. In addition, CK2 activity has been associated with cardiovascular diseases, as cardiac ischemia-reperfusion injury, atherosclerosis, and cardiac hypertrophy. The hypothesis of considering CK2 inhibition for cystic fibrosis therapies has been also entertained for many years. Moreover, psychiatric disorders and syndromes due to CK2 mutations have been recently identified. On these bases, CK2 is emerging as an increasingly attractive target in various fields of human medicine, with the advantage that several very specific and effective inhibitors are already available. Here, we review the literature on CK2 implication in different human pathologies and evaluate its potential as a pharmacological target in the light of the most recent findings.
引用
收藏
页数:20
相关论文
共 339 条
[91]  
FIRZLAFF J M, 1989, New Biologist, V1, P44
[92]   Kinases, tails and more: Regulation of PTEN function by phosphorylation [J].
Fragoso, Rita ;
Barata, Joao T. .
METHODS, 2015, 77-78 :75-81
[93]   An AUTS2-Polycomb complex activates gene expression in the CNS [J].
Gao, Zhonghua ;
Lee, Pedro ;
Stafford, James M. ;
von Schimmelmann, Melanie ;
Schaefer, Anne ;
Reinberg, Danny .
NATURE, 2014, 516 (7531) :349-+
[94]   ASSOCIATION OF ELEVATED PROTEIN-KINASE CK2 ACTIVITY WITH AGGRESSIVE-BEHAVIOR OF SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK [J].
GAPANY, M ;
FAUST, RA ;
TAWFIC, S ;
DAVIS, A ;
ADAMS, GL ;
AHMED, K .
MOLECULAR MEDICINE, 1995, 1 (06) :659-666
[95]   Protein Kinase CK2: An Emerging Regulator of Immunity [J].
Gibson, Sara A. ;
Benveniste, Etty N. .
TRENDS IN IMMUNOLOGY, 2018, 39 (02) :82-85
[96]   Protein kinase CK2α subunit over-expression correlates with metastatic risk in breast carcinomas: Quantitative immunohistochemistry in tissue microarrays [J].
Giusiano, Sophie ;
Cachet, Claude ;
Filhol, Odile ;
Duchemin-Pelletier, Eve ;
Secq, Veronique ;
Bonnier, Pascal ;
Carcopino, Xavier ;
Boubli, Leon ;
Birnbaum, Daniel ;
Garcia, Stephane ;
Iovanna, Juan ;
Charpin, Colette .
EUROPEAN JOURNAL OF CANCER, 2011, 47 (05) :792-801
[97]   Inhibition of protein kinase CK2 leads to a modulation of androgen receptor dependent transcription in prostate cancer cells [J].
Goetz, Claudia ;
Bachmann, Christa ;
Montenarh, Mathias .
PROSTATE, 2007, 67 (02) :125-134
[98]   Improved ATM kinase inhibitor KU-60019 radiosensitizes glioma cells, compromises insulin, AKT and ERK prosurvival signaling, and inhibits migration and invasion [J].
Golding, Sarah E. ;
Rosenberg, Elizabeth ;
Valerie, Nicholas ;
Hussaini, Isa ;
Frigerio, Mark ;
Cockcroft, Xiaoling F. ;
Chong, Wei Yee ;
Hummersone, Marc ;
Rigoreau, Laurent ;
Menear, Keith A. ;
O'Connor, Mark J. ;
Povirk, Lawrence F. ;
van Meter, Timothy ;
Valerie, Kristoffer .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (10) :2894-2902
[99]   A SARS-CoV-2 protein interaction map reveals targets for drug repurposing [J].
Gordon, David E. ;
Jang, Gwendolyn M. ;
Bouhaddou, Mehdi ;
Xu, Jiewei ;
Obernier, Kirsten ;
White, Kris M. ;
O'Meara, Matthew J. ;
Rezelj, Veronica V. ;
Guo, Jeffrey Z. ;
Swaney, Danielle L. ;
Tummino, Tia A. ;
Huttenhain, Ruth ;
Kaake, Robyn M. ;
Richards, Alicia L. ;
Tutuncuoglu, Beril ;
Foussard, Helene ;
Batra, Jyoti ;
Haas, Kelsey ;
Modak, Maya ;
Kim, Minkyu ;
Haas, Paige ;
Polacco, Benjamin J. ;
Braberg, Hannes ;
Fabius, Jacqueline M. ;
Eckhardt, Manon ;
Soucheray, Margaret ;
Bennett, Melanie J. ;
Cakir, Merve ;
McGregor, Michael J. ;
Li, Qiongyu ;
Meyer, Bjoern ;
Roesch, Ferdinand ;
Vallet, Thomas ;
Mac Kain, Alice ;
Miorin, Lisa ;
Moreno, Elena ;
Naing, Zun Zar Chi ;
Zhou, Yuan ;
Peng, Shiming ;
Shi, Ying ;
Zhang, Ziyang ;
Shen, Wenqi ;
Kirby, Ilsa T. ;
Melnyk, James E. ;
Chorba, John S. ;
Lou, Kevin ;
Dai, Shizhong A. ;
Barrio-Hernandez, Inigo ;
Memon, Danish ;
Hernandez-Armenta, Claudia .
NATURE, 2020, 583 (7816) :459-+
[100]   Preclinical efficacy of CIGB-300, an anti-CK2 peptide, on breast cancer metastasic colonization [J].
Gottardo, Maria F. ;
Capobianco, Carla S. ;
Sidabra, Johanna E. ;
Garona, Juan ;
Perera, Yasser ;
Perea, Silvio E. ;
Alonso, Daniel F. ;
Farina, Hernan G. .
SCIENTIFIC REPORTS, 2020, 10 (01)