[HTML][HTML] The JNK signaling pathway in inflammatory skin disorders and cancer

MB Hammouda, AE Ford, Y Liu, JY Zhang - Cells, 2020 - mdpi.com
The c-Jun N-terminal kinases (JNKs), with its members JNK1, JNK2, and JNK3, is a
subfamily of (MAPK) mitogen-activated protein kinases. JNK signaling regulates a wide …

Targeting extracellular signal-regulated protein kinase 1/2 (ERK1/2) in cancer: an update on pharmacological small-molecule inhibitors

L Fu, S Chen, G He, Y Chen, B Liu - Journal of Medicinal …, 2022 - ACS Publications
Extracellular signal-regulated protein kinase 1/2 (ERK1/2), the only known substrate of
MEK1/2, is located downstream of the RAS-RAF-MEK-ERK (MAPK) pathway and is …

CDK2 and CDK4: Cell cycle functions evolve distinct, catalysis-competent conformations, offering drug targets

W Zhang, Y Liu, H Jang, R Nussinov - JACS Au, 2024 - ACS Publications
Cyclin-dependent kinases (CDKs), particularly CDK4 and CDK2, are crucial for cell cycle
progression from the Gap 1 (G1) to the Synthesis (S) phase by phosphorylating targets such …

Targeting ERK-MYD88 interaction leads to ERK dysregulation and immunogenic cancer cell death

F Virard, S Giraud, M Bonnet, L Magadoux… - Nature …, 2024 - nature.com
The quest for targeted therapies is critical in the battle against cancer. The RAS/MAP kinase
pathway is frequently implicated in neoplasia, with ERK playing a crucial role as the most …

Targeting a key protein-protein interaction surface on mitogen-activated protein kinases by a precision-guided warhead scaffold

ÁL Póti, D Bálint, A Alexa, P Sok, K Ozsváth… - Nature …, 2024 - nature.com
For mitogen-activated protein kinases (MAPKs) a shallow surface—distinct from the
substrate binding pocket—called the D (ocking)-groove governs partner protein binding …

Targeting SMAD-dependent signaling: considerations in epithelial and mesenchymal solid tumors

F Runa, G Ortiz-Soto, NR de Barros, JA Kelber - Pharmaceuticals, 2024 - mdpi.com
SMADs are the canonical intracellular effector proteins of the TGF-β (transforming growth
factor-β). SMADs translocate from plasma membrane receptors to the nucleus regulated by …

Structure-Guided Discovery and Preclinical Assessment of Novel (Thiophen-3-yl) aminopyrimidine Derivatives as Potent ERK1/2 Inhibitors

W Shuai, H **ao, P Yang, Y Zhang, F Bu… - Journal of Medicinal …, 2024 - ACS Publications
The RAS-RAF-MEK-ERK signaling cascade is abnormally activated in various tumors,
playing a crucial role in mediating tumor progression. As the key component at the terminal …

Development of 2′-aminospiro [pyrano [3, 2–c] quinoline]-3′-carbonitrile derivatives as non-ATP competitive Src kinase inhibitors that suppress breast cancer cell …

M Ramadan, YAMM Elshaier, AA Aly, M Abdel-Aziz… - Bioorganic …, 2021 - Elsevier
Src kinase activity controls diverse cellular functions, including cell growth, migration,
adhesion, and survival. It is de-regulated in several cancers, including breast cancer, where …

[HTML][HTML] Phosphorylation-Assisted Luciferase Complementation Assay Designed to Monitor Kinase Activity and Kinase-Domain-Mediated Protein–Protein Binding

ÁL Póti, L Dénes, K Papp, C Bató, Z Bánóczi… - International Journal of …, 2023 - mdpi.com
Protein kinases are key regulators of cell signaling and have been important therapeutic
targets for three decades. ATP-competitive drugs directly inhibit the activity of kinases but …

MR1 gene and protein expression are enhanced by inhibition of the extracellular signal-regulated kinase ERK

D Constantin, V Nosi, N Kehrer, A Vacchini… - Cancer Immunology …, 2024 - aacrjournals.org
The MHC class I–related molecule MR1 is ubiquitously expressed, is highly conserved
among mammals, and presents bacterial and endogenous antigens in tumor cells. These …