Mitochondrial Dysfunction in Cardiotoxicity Induced by BCR-ABL1 Tyrosine Kinase Inhibitors -Underlying Mechanisms, Detection, Potential Therapies

S Sun, J Qin, W Liao, X Gao, Z Shang, D Luo… - Cardiovascular …, 2023 - Springer
The advent of BCR-ABL tyrosine kinase inhibitors (TKIs) targeted therapy revolutionized the
treatment of chronic myeloid leukemia (CML) patients. Mitochondria are the key organelles …

Cardiovascular toxicity in antitumor therapy: biological and therapeutic insights

X Lin, X Ma, S Zhao, J Yao, L Han, Y Jing, X Xue - Trends in Cancer, 2024 - cell.com
The evolution of antitumor therapies has significantly improved cancer prognosis but has
concurrently resulted in cardiovascular toxicities. Understanding the biological mechanisms …

Designing novel BCR-ABL inhibitors for chronic myeloid leukemia with improved cardiac safety

M Pandrala, AAN Bruyneel, AP Hnatiuk… - Journal of medicinal …, 2022 - ACS Publications
Development of tyrosine kinase inhibitors (TKIs) targeting the BCR-ABL oncogene
constitutes an effective approach for the treatment of chronic myeloid leukemia (CML) and/or …

Integrated Stress Response Potentiates Ponatinib-Induced Cardiotoxicity

G Yan, Z Han, Y Kwon, J Jousma, SB Nukala… - Circulation …, 2024 - Am Heart Assoc
BACKGROUND: Mitochondrial dysfunction is a primary driver of cardiac contractile failure;
yet, the cross talk between mitochondrial energetics and signaling regulation remains …

Off-target pharmacological activity at various kinases: Potential functional and pathological side effects

JR Green, PKS Mahalingaiah… - … of Pharmacological and …, 2023 - Elsevier
In drug discovery, during the lead optimization and candidate characterization stages, novel
small molecules are frequently evaluated in a battery of in vitro pharmacology assays to …

[HTML][HTML] Empagliflozin mitigates ponatinib-induced cardiotoxicity by restoring the connexin 43-autophagy pathway

L Mattii, S Moscato, C Ippolito, E Polizzi, G Novo… - Biomedicine & …, 2024 - Elsevier
Background Empagliflozin (EMPA), a selective sodium-glucose cotransporter type 2
(SGLT2) inhibitor, has been shown to reduce major adverse cardiovascular events in …

The role of deubiquitinases in cardiac disease

X Zhan, Y Yang, Q Li, F He - Expert Reviews in Molecular Medicine, 2024 - cambridge.org
Deubiquitinases are a group of proteins that identify and digest monoubiquitin chains or
polyubiquitin chains attached to substrate proteins, preventing the substrate protein from …

Exploring the Potential of Azo Compounds in Leukemia Treatment: Synthesis and Characterization of New Derivatives with Dimedone and Meldrum's Acid End …

Y Güney, Ö Dilek, B Sezgin, T Tilki - ChemistrySelect, 2023 - Wiley Online Library
This scholarly investigation presents pioneering drug candidates for combating leukemia,
distinguished by reduced side effects and elevated efficacy. The study focuses on azo …

ThermoTargetMiner as a proteome integral solubility alteration target database for prospective drugs against lung cancer

H Lyu, H Gharibi, B Sokolova, A Voiland, B Nilsson… - bioRxiv, 2024 - biorxiv.org
Knowledge of the targets of therapeutic compounds is vital for understanding their action
mechanisms and side effects, but such valuable data is seldom available. The multiple …

Imidazole Based Novel Schiff Base: Synthesis, Characterization, Quantum Chemical Calculations, In Silico Investigation of ADMEt Properties and Molecular Docking …

Ö Dilek - Bitlis Eren Üniversitesi Fen Bilimleri Dergisi - dergipark.org.tr
The potential drug candidate novel Schiff base, 2-(((3-(4-methyl-1H-imidazol-1-yl)-5-
(trifluoromethyl) phenyl) imino) methyl) phenol (MITPIM) was synthesized by the reaction of …