Differential functions of ERK1 and ERK2 in lung metastasis processes in triple-negative breast cancer

M Gagliardi, MK Pitner, J Park, X Xie, H Saso… - Scientific reports, 2020 - nature.com
Triple-negative breast cancer (TNBC) is an aggressive form of breast cancer characterized
by metastasis, drug resistance and high rates of recurrence. With a lack or targeted …

Design, synthesis and biological evaluation of fused naphthofuro [3, 2-c] quinoline-6, 7, 12-triones and pyrano [3, 2-c] quinoline-6, 7, 8, 13-tetraones derivatives as …

AA Aly, EM El-Sheref, MEM Bakheet, MAE Mourad… - Bioorganic …, 2019 - Elsevier
Approximately 60% of human cancers exhibit enhanced activity of ERK1 and ERK2,
reflecting their multiple roles in tumor initiation and progression. Acquired drug resistance …

Vanadium Selenide Nanobelt Electrocatalyst for Dopamine-Selective Detection

S Chae, C Woo, GH Gu, TY Kim, J Jeon… - ACS Applied Nano …, 2023 - ACS Publications
Electrochemical dopamine (DA) detection has been extensively studied for the practical
diagnosis of neurological disorders. A major challenge in this system is to synthesize …

Functional built-in template directed siliceous fluorescent supramolecular vesicles as diagnostics

J Li, K Liu, H Chen, R Li, M Drechsler… - … Applied Materials & …, 2017 - ACS Publications
Functional template directed synthesis of hybrid siliceous fluorescent vesicle (HSFV) is
fabricated by using fluorescent vesicle as a built-in template. The template vesicle is the …

Modulating multi-functional ERK complexes by covalent targeting of a recruitment site in vivo

TS Kaoud, WH Johnson, ND Ebelt, A Piserchio… - Nature …, 2019 - nature.com
Recently, the targeting of ERK with ATP-competitive inhibitors has emerged as a potential
clinical strategy to overcome acquired resistance to BRAF and MEK inhibitor combination …

Structural and dynamic features of F-recruitment site driven substrate phosphorylation by ERK2

A Piserchio, V Ramakrishan, H Wang, TS Kaoud… - Scientific reports, 2015 - nature.com
The F-recruitment site (FRS) of active ERK2 binds F-site (Phe-x-Phe-Pro) sequences found
downstream of the Ser/Thr phospho-acceptor on cellular substrates. Here we apply NMR …

Quantification of ERK kinase activity in biological samples using differential sensing

D Zamora-Olivares, TS Kaoud, L Zeng… - ACS chemical …, 2019 - ACS Publications
The understanding of complex biological systems requires an ability to evaluate interacting
networks of genes, proteins, and cellular reactions. Enabling technologies that support the …

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 …

A real-time, fluorescence-based assay for Rho-associated protein kinase activity

MI Kelly, TJ Bechtel, DR Reddy, ED Hankore… - Analytica Chimica …, 2015 - Elsevier
Inhibitors of Rho-associated protein kinase (ROCK) enzymatic activity have been shown to
reduce the invasive phenotype observed in metastatic hepatocellular carcinoma (HCC). We …

Design and evaluation of a real-time activity probe for focal adhesion kinase

JR Beck, X Zhou, GR Casey, CI Stains - Analytica Chimica Acta, 2015 - Elsevier
Focal adhesion kinase (FAK) has been identified as a potential therapeutic target for the
treatment of metastatic cancers. Herein we describe the design, synthesis and optimization …