[HTML][HTML] CK1δ modulates the transcriptional activity of ERα via AIB1 in an estrogen-dependent manner and regulates ERα–AIB1 interactions

G Giamas, L Castellano, Q Feng… - Nucleic acids …, 2009 - ncbi.nlm.nih.gov
Oncogenesis in breast cancer often requires the overexpression of the nuclear receptor
coactivator AIB1/SRC-3 acting in conjunction with estrogen receptor-α (ERα) …

Unlocking New Avenues in Breast Cancer Treatment: The Synergy of Kinase Inhibitors and Immunotherapy

MJ Bravo, AM Burgos-Molina, M García-Aranda… - Cancers, 2023 - mdpi.com
Simple Summary Recent research has revealed a possible synergy between kinase
inhibitors and immunotherapy in the treatment of breast cancer. Kinase inhibitors can …

New halogenated constituents from Mangifera zeylanica Hook. f. and their potential anti-cancer effects in breast and ovarian cancer cells

MK Ediriweera, KH Tennekoon, A Adhikari… - Journal of …, 2016 - Elsevier
Abstract Ethnopharmacological relevence Mangifera zeylanica Hook. f.(Anacardiaceae) is a
plant endemic to Sri Lanka. Its bark has been used in traditional and Ayurvedic medicine for …

Integrin αvβ3 upregulates integrin‐linked kinase expression in human ovarian cancer cells via enhancement of ILK gene transcription

D Loessner, C Abou‐Ajram, A Benge… - Journal of cellular …, 2009 - Wiley Online Library
We previously showed that integrin αvβ3 overexpression and engagement by its ligand
vitronectin increased adhesion, motility, and proliferation of human ovarian cancer cells. In …

Redox mechanism, spectrophotometrical characterisation and voltammetric determination in serum samples of kinases inhibitor and anticancer drug dasatinib

CSH Jesus, VC Diculescu - Journal of Electroanalytical Chemistry, 2015 - Elsevier
The electrochemical oxidation mechanism of the anticancer drug and kinases inhibitor
dasatinib was studied by cyclic, differential pulse and square wave voltammetry using a …

Drugging the Plasmodium kinome: The benefits of academia–industry synergy

D Leroy, C Doerig - Trends in pharmacological sciences, 2008 - cell.com
Malaria remains a major killer in many parts of the world. Recently, the development of
nonprofit organisations aimed at fighting this deadly scourge incited academic and industrial …

Structure-based virtual screening of high-affinity ATP-competitive inhibitors against human lemur tyrosine kinase-3 (LMTK3) domain: a novel therapeutic target for …

H Sarma, VSK Mattaparthi - Interdisciplinary Sciences: Computational Life …, 2019 - Springer
Human lemur tyrosine kinase-3 (LMTK3) is an oncogenic kinase known to regulate ER-α
through phosphorylation and is considered to be a novel therapeutic target for breast …

Discovery of novel dual inhibitors of receptor tyrosine kinases EGFR and PDGFR-β related to anticancer drug resistance

T Fischer, A Najjar, F Totzke, C Schächtele… - Journal of Enzyme …, 2018 - Taylor & Francis
With ongoing resistance problems against the marketed EGFR inhibitors having a
quinazoline core scaffold there is a need for the development of novel inhibitors having a …

Synthesis, kinetics and cellular studies of new phenothiazine analogs as potent human-TLK inhibitors

D Johnson, J Hussain, S Bhoir… - Organic & …, 2023 - pubs.rsc.org
The alterations in the expression patterns of protein kinases often implicate human cancer
initiation and progression. Human tousled-like kinases (TLKs), both TLK1/1B and TLK2, are …

Design, synthesis and evaluation of acridone-2-carbohydrazide derivatives as p-AKT Ser473 kinase inhibitors

TT Yadav, MS Kumar, S Bajaj, M Yc - Future Medicinal Chemistry, 2023 - Future Science
Aim: A series of benzylidene-and phenylethylidene-substituted acridone-2-carbohydrazide
derivatives were designed, synthesized and evaluated for their cytotoxicity and response to …