Anticancer activity of electron-deficient metal complexes against colorectal cancer in vitro models

Azmanova, Maria, Soldevila‐Barreda, Joan, Hani, Hira Bani, Lord, Rianne M. ORCID: https://orcid.org/0000-0001-9981-129X, Pitto‐Barry, Anaïs, Picksley, Steven M. and Barry, Nicolas P. E. (2019) Anticancer activity of electron-deficient metal complexes against colorectal cancer in vitro models. ChemMedChem, 14 (22). pp. 1887-1893. ISSN 1860-7179

Full text not available from this repository.

Abstract

An evaluation of the in vitro cytotoxicity of nine electron‐deficient half‐sandwich metal complexes towards two colorectal cancer cell lines (HCT116 p53+/+, HCT116 p53−/−) and one normal prostate cell line (PNT2) is presented herein. Three complexes were found to be equally cytotoxic towards both colorectal cancer cell lines, suggesting a p53‐independent mechanism of action. These complexes are 12 to 34× more potent than cisplatin against HCT116 p53+/+ and HCT116 p53−/− cells. Furthermore, they were found to exhibit little or no cytotoxicity towards PNT2 normal cells, with selectivity ratios greater than 50. To gain an insight into the potential mechanisms of action of the most active compounds, their effects on the expression levels of a panel of genes were measured using qRT‐PCR against treated HCT116 p53+/+ and HCT116 p53−/− cells, and cell‐cycle analysis was carried out.

Item Type: Article
Uncontrolled Keywords: sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being
Faculty \ School: Faculty of Science > School of Chemistry (former - to 2024)
UEA Research Groups: Faculty of Science > Research Groups > Chemistry of Materials and Catalysis
Faculty of Science > Research Groups > Chemistry of Life Processes
Faculty of Science > Research Centres > Centre for Molecular and Structural Biochemistry
Related URLs:
Depositing User: LivePure Connector
Date Deposited: 30 Jan 2020 04:15
Last Modified: 25 Sep 2024 14:28
URI: https://ueaeprints.uea.ac.uk/id/eprint/73865
DOI: 10.1002/cmdc.201900528

Actions (login required)

View Item View Item