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

被引:196
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.
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页数:20
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共 339 条
  • [11] The Thr205 Phosphorylation Site within Respiratory Syncytial Virus Matrix (M) Protein Modulates M Oligomerization and Virus Production
    Bajorek, M.
    Caly, L.
    Tran, K. C.
    Maertens, G. N.
    Tripp, R. A.
    Bacharach, E.
    Teng, M. N.
    Ghildyal, R.
    Jans, D. A.
    [J]. JOURNAL OF VIROLOGY, 2014, 88 (11) : 6380 - 6393
  • [12] Mammalian FMRP S499 Is Phosphorylated by CK2 and Promotes Secondary Phosphorylation of FMRP
    Bartley, Christopher M.
    O'Keefe, Rachel A.
    Blice-Baum, Anna
    Mihailescu, Mihaela-Rita
    Gong, Xuan
    Miyares, Laura
    Karaca, Esra
    Bordey, Angelique
    [J]. ENEURO, 2016, 3 (06)
  • [13] Encephalomyocarditis Virus Leader Is Phosphorylated by CK2 and Syk as a Requirement for Subsequent Phosphorylation of Cellular Nucleoporins
    Basta, Holly A.
    Bacot-Davis, Valjean R.
    Ciomperlik, Jessica J.
    Palmenberg, Ann C.
    [J]. JOURNAL OF VIROLOGY, 2014, 88 (04) : 2219 - 2226
  • [14] Structural features underlying selective inhibition of protein kinase CK2 by ATP site-directed tetrabromo-2-benzotriazole
    Battistutta, R
    De Moliner, E
    Sarno, S
    Zanotti, G
    Pinna, LA
    [J]. PROTEIN SCIENCE, 2001, 10 (11) : 2200 - 2206
  • [15] Unprecedented Selectivity and Structural Determinants of a New Class of Protein Kinase CK2 Inhibitors in Clinical Trials for the Treatment of Cancer
    Battistutta, Roberto
    Cozza, Giorgio
    Pierre, Fabrice
    Papinutto, Elena
    Lolli, Graziano
    Sarno, Stefania
    O'Brien, Sean E.
    Siddiqui-Jain, Adam
    Haddach, Mustapha
    Anderes, Kenna
    Ryckman, David M.
    Meggio, Flavio
    Pinna, Lorenzo A.
    [J]. BIOCHEMISTRY, 2011, 50 (39) : 8478 - 8488
  • [16] CIGB-300, an anti-CK2 peptide, inhibits angiogenesis, tumor cell invasion and metastasis in lung cancer models
    Benavent Acero, Fernando
    Capobianco, Carla S.
    Garona, Juan
    Cirigliano, Stefano M.
    Perera, Yasser
    Urtreger, Alejandro J.
    Perea, Silvio E.
    Alonso, Daniel F.
    Farina, Hernan G.
    [J]. LUNG CANCER, 2017, 107 : 14 - 21
  • [17] Bender M, 2017, HELIYON, V3, DOI 10.1016/j.heliyon.2017.e00318
  • [18] IN VIVO MODULATION OF POLO-LIKE KINASES SUPPORTS A KEY ROLE FOR PLK2 IN SER129 α-SYNUCLEIN PHOSPHORYLATION IN MOUSE BRAIN
    Bergeron, M.
    Motter, R.
    Tanaka, P.
    Fauss, D.
    Babcock, M.
    Chiou, S. -S.
    Nelson, S.
    San Pablo, F.
    Anderson, J. P.
    [J]. NEUROSCIENCE, 2014, 256 : 72 - 82
  • [19] Demonstration of subcellular migration of CK2α localization from nucleus to sarco(endo)plasmic reticulum in mammalian cardiomyocytes under hyperglycemia
    Bitirim, Ceylan Verda
    Tuncay, Erkan
    Turan, Belma
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2018, 443 (1-2) : 25 - 36
  • [20] Protein kinase CK2 inhibition as a pharmacological strategy
    Borgo, Christian
    Ruzzene, Maria
    [J]. ADVANCES IN PROTEIN CHEMISTRY AND STRUCTURAL BIOLOGY, VOL 124: PROTEIN KINASES IN DRUG DISCOVERY, 2021, 124 : 23 - 46