Mechanistic basis of enzyme-targeted drugs

JG Robertson - Biochemistry, 2005 - ACS Publications
Enzymes offer unique opportunities for drug design that are not available to cell surface
receptors, nuclear hormone receptors, ion channels, transporters, and DNA. Here, we …

Adverse drug reactions of anticancer drugs derived from natural sources

D Tewari, P Rawat, PK Singh - Food and Chemical Toxicology, 2019 - Elsevier
Cancer, a life threatening disease adversely affects huge population worldwide. Naturally
derived drug discovery has emerged as a potential pathway in search of anticancers …

A marine terpenoid, heteronemin, induces both the apoptosis and ferroptosis of hepatocellular carcinoma cells and involves the ROS and MAPK pathways

WT Chang, YD Bow, PJ Fu, CY Li… - Oxidative medicine …, 2021 - Wiley Online Library
Hepatocellular carcinoma (HCC) is a leading cause of death, resulting in over 700 thousand
deaths annually worldwide. Chemotherapy is the primary therapeutic strategy for patients …

ABT-263: a potent and orally bioavailable Bcl-2 family inhibitor

C Tse, AR Shoemaker, J Adickes, MG Anderson… - Cancer research, 2008 - AACR
Overexpression of the prosurvival Bcl-2 family members (Bcl-2, Bcl-xL, and Mcl-1) is
commonly associated with tumor maintenance, progression, and chemoresistance. We …

Bambu and its applications in the discovery of active molecules against melanoma

IL Guidotti, A Neis, DP Martinez, FK Seixas… - Journal of Molecular …, 2023 - Elsevier
Purpose or objective Melanoma is one of the most dangerous forms of skin cancer and the
discovery of novel drugs is an ongoing effort. Quantitative Structure Activity Relationship …

Curcumin in cancer and inflammation: an in-depth exploration of molecular interactions, therapeutic potentials, and the role in disease management

DO Moon - International Journal of Molecular Sciences, 2024 - mdpi.com
This paper delves into the diverse and significant roles of curcumin, a polyphenolic
compound from the Curcuma longa plant, in the context of cancer and inflammatory …

Discovery of novel polycyclic heterocyclic derivatives from evodiamine for the potential treatment of triple-negative breast cancer

S Xu, H Yao, Y Qiu, M Zhou, D Li, L Wu… - Journal of Medicinal …, 2021 - ACS Publications
Evodiamine (Evo) is a quinazolinocarboline alkaloid found in Evodia rutaecarpa and
exhibits moderate antiproliferative activity. Herein, we report using a scaffold-hopping …

Selective topotecan delivery to cancer cells by targeted pH-sensitive mesoporous silica nanoparticles

M Martínez-Carmona, D Lozano, M Colilla… - RSC …, 2016 - pubs.rsc.org
Topotecan (TOP), a water-soluble derivative of camptothecin, is a potent antitumor agent
that is receiving growing attention for the treatment of several types of cancer. However, one …

[HTML][HTML] High glucose-induced oxidative stress accelerates myogenesis by altering SUMO reactions

X Liu, G Heras, VM Lauschke, J Mi, G Tian… - Experimental Cell …, 2020 - Elsevier
Skeletal muscle preservation is a dynamic process that involves constant repair and
regeneration. However, the regenerative capacity of muscle cells declines in hyperglycemia …

FTY720 inhibits tumor growth and enhances the tumor‐suppressive effect of topotecan in neuroblastoma by interfering with the sphingolipid signaling pathway

MH Li, T Hla, F Ferrer - Pediatric blood & cancer, 2013 - Wiley Online Library
Background Neuroblastoma (NB) is the most common extra‐cranial solid tumor in
childhood. Poor outcomes for children with advanced disease underscore the need for novel …