[HTML][HTML] Doxorubicin, DNA torsion, and chromatin dynamics

F Yang, SS Teves, CJ Kemp, S Henikoff - Biochimica et Biophysica Acta …, 2014 - Elsevier
Doxorubicin is one of the most important anti-cancer chemotherapeutic drugs, being widely
used for the treatment of solid tumors and acute leukemias. The action of doxorubicin and …

Genotoxicity of non-covalent interactions: DNA intercalators

LR Ferguson, WA Denny - Mutation Research/Fundamental and Molecular …, 2007 - Elsevier
This review provides an update on the mutagenicity of intercalating chemicals, as carried out
over the last 17 years. The most extensively studied DNA intercalating agents are acridine …

[HTML][HTML] Doxorubicin enhances nucleosome turnover around promoters

F Yang, CJ Kemp, S Henikoff - Current Biology, 2013 - cell.com
Doxorubicin is an anthracycline DNA intercalator that is among the most commonly used
anticancer drugs [1]. Doxorubicin causes DNA double-strand breaks in rapidly dividing cells …

Single molecule tracking based drug screening

D Watanabe, M Hiroshima, M Yasui, M Ueda - Nature Communications, 2024 - nature.com
The single-molecule tracking of transmembrane receptors in living cells has provided
significant insights into signaling mechanisms, such as mobility and clustering upon their …

[HTML][HTML] Resistance mechanism of acute myeloid leukemia cells against daunorubicin and cytarabine: a literature review

EY Arwanih, M Louisa, I Rinaldi, SI Wanandi - Cureus, 2022 - ncbi.nlm.nih.gov
Acute myeloid leukemia (AML) is a hematological malignancy commonly found in adult
patients. Low overall survival and resistance to therapy are the main issues in AML. The first …

Design, synthesis and biological evaluation of novel perimidine o-quinone derivatives as non-intercalative topoisomerase II catalytic inhibitors

DC Zhou, YT Lu, YW Mai, C Zhang, J Xia, PF Yao… - Bioorganic …, 2019 - Elsevier
For the development of novel anticancer agents, we designed and synthesized a total of 37
perimidine o-quinone derivatives containing the o-quinone group at the A or B ring and …

Dual inhibition: a novel promising pharmacological approach for different disease conditions

S Patyar, A Prakash, B Medhi - Journal of Pharmacy and …, 2011 - academic.oup.com
To overcome the problems associated with polypharmacy, which include medication non
compliance, adverse drug reactions, drug–drug interactions and increased pill-burden …

Characterization of DNA reactive and non-DNA reactive anticancer drugs by gene expression profiling

AC Le Fevre, E Boitier, JP Marchandeau… - Mutation Research …, 2007 - Elsevier
Gene expression profiling technology is expected to advance our understanding of
genotoxic mechanisms involving direct or indirect interaction with DNA. We exposed human …

Zinc differentially modulates DNA damage induced by anthracyclines in normal and cancer cells

D Wysokinski, J Blasiak, K Wozniak - Experimental Oncology, 2012 - dspace.nbuv.gov.ua
Zinc is one of the most essential trace elements in human organism. Low blood level of zinc
is often noted in acute lymphocytic leukemia (ALL). Treatment with zinc adjuvant is …

Assessment of the (anti) genotoxicity of brown propolis extracts from Brazilian Cerrado biome in a Drosophila melanogaster model

FH Fernandes, Z da Rosa Guterres, WS Garcez… - Food Research …, 2014 - Elsevier
Among the great number of studies on the chemical and biological features of propolis from
Brazil, none have been found on the evaluation of the biological properties of propolis from …