| Literature DB >> 29174576 |
Sinara Mônica Vitalino de Almeida1, Amélia Galdino Ribeiro2, Geilza Carla de Lima Silva3, Josival Emanuel Ferreira Alves3, Eduardo Isidoro Carneiro Beltrão3, Jamerson Ferreira de Oliveira2, Luiz Bezerra de Carvalho3, Maria do Carmo Alves de Lima4.
Abstract
DNA is considered one of the most promising targets of molecules with anticancer activity potential. Its key role in various cell division mechanisms, which commands the intense multiplication of tumor cells, is considered in studies with compounds whose mechanisms of action suggest likeliness of interaction. In addition, inhibition of enzymes that actively participate in biological functions of cells such as Topoisomerase, is seen as a primary factor for conducting several events that result in cell death. Discovery of new anticancer chemotherapeutical capable of interacting with DNA and inhibiting Topoisomerase enzymes is highlighted in anticancer research. The present review aims at showing through distinct biological tests the performance of different candidates to anticancer drugs and their respective chemical modifications, which are crucial and/or determinant for DNA affinity and inhibition of important enzymes in cells' vital processe to either separately or synergistically optimize anticancer activity.Entities:
Keywords: Acridine derivatives; DNA-topoisomerase; Metallic compounds; Nitrogenous heterocyclic derivatives; Thiosemicarbazone
Mesh:
Substances:
Year: 2017 PMID: 29174576 DOI: 10.1016/j.biopha.2017.11.054
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529