[HTML][HTML] In vitro combinatorial anti-proliferative and immunosuppressive effects of Brucea javanica extract with CX-4945 and imatinib in human T-cell acute …

JI Jung, SY Kim, KY Park, K Sydara, SW Lee… - Biomedicine & …, 2018 - Elsevier
Since 1970, the isolated and identified components of Brucea javanica (L.) Merr. have been
known to contain anticancer effects, particularly antileukemic effect. In this study, the …

Protein Kinase CK2: at the crossroads of pathways controlling cell proliferation and survival

M Gabriel, DW Litchfield - Protein kinase CK2, 2013 - Wiley Online Library
Cells exist in a dynamic state; they require the ability to rapidly adapt to their constantly
changing environment. Responses to these changes are mediated by signal transduction …

Effects of CK2 inhibition in cultured fibroblasts from Type 1 Diabetic patients with or without nephropathy

E Iori, M Ruzzene, S Zanin, S Sbrignadello… - Growth …, 2015 - Taylor & Francis
CK2 is a multifunctional, pleiotropic protein kinase involved in the regulation of cell
proliferation and survival. Since fibroblasts from Type 1 Diabetes patients (T1DM) with …

Inhibitory properties of ATP-competitive coumestrol and boldine are correlated to different modulations of CK2 flexibility

R Battistutta, G Lolli - Journal of natural products, 2019 - ACS Publications
Casein kinase 2 (CK2) is an anti-apoptotic cancer-sustaining protein kinase. Its
crystallographic structures with the natural compounds coumestrol, a phytoestrogen, and …

Design, synthesis and biological evaluation of 2-aminopyrimidinones and their 6-aza-analogs as a new class of CK2 inhibitors

MO Chekanov, OV Ostrynska… - Journal of Enzyme …, 2014 - Taylor & Francis
In order to find the new potent CK2 inhibitors the 60 derivatives of 2-aminopyrimidinone and
their 6-aza-substituted analogs were synthesized and tested in vitro. Among them, the most …

Rational design of coumarin derivatives as CK2 inhibitors by improving the interaction with the hinge region

N Zhang, W Chen, Y Zhou, H Zhao… - Molecular …, 2016 - Wiley Online Library
Abstract Design of novel coumarin derivatives as CK2 inhibitors were attempted by targeting
the interaction with the hinge region. A set of substituents capable of forming a hydrogen …

[PDF][PDF] 蛋白激酶CK2 与人类恶性肿瘤

PK CK - pdfs.semanticscholar.org
恶性肿瘤严重威胁人类健康和生命, 影响社会经济的发展. 随着研究的深入,
恶性肿瘤发生发展机制, 生物学行为调控机理不断被揭示, 新的药物靶点陆续被发现 …

Unleashing the guardian: the targetable BCR-ABL/HAUSP/PML/PTEN network in chronic myeloid leukemia

A Morotti, D Torti, G Carra, C Panuzzo… - Current Drug …, 2017 - ingentaconnect.com
The complete eradication of Chronic Myeloid Leukemia is still challenging even in the era of
highly selective and potent BCR-ABL tyrosine kinase inhibitors (TKIs). The 'Achilles heel'of …

[PDF][PDF] Mecanismo de acción antineoplásico del CIGB-300, péptido inhibidor de la proteína quinasa CK2, en células de leucemia mieloide aguda

MR Menzoney - 2023 - accesoabierto.uh.cu
La leucemia mieloide aguda (LMA) es una neoplasia hematológica que se caracteriza por
la proliferación descontrolada de progenitores mieloides indiferenciados, y el desarrollo de …

[HTML][HTML] Modulation of immunosuppression by oligonucleotide-based molecules and small molecules targeting myeloid-derived suppressor cells

J Lim, A Lee, HG Lee, JS Lim - Biomolecules & Therapeutics, 2020 - ncbi.nlm.nih.gov
Myeloid-derived suppressor cells (MDSCs) are immature myeloid cells that exert
suppressive function on the immune response. MDSCs expand in tumor-bearing hosts or in …