Novel Thiazolidine-2,4-dione-trimethoxybenzene-thiazole Hybrids as Human Topoisomerases Inhibitors.
Maria Stefania SinicropiJessica CeramellaPatrice VanelleDomenico IacopettaCamillo RosanoOmar KhoumeriShawkat AbdelmohsenWafaa AbdelhadyHussein El-KashefPublished in: Pharmaceuticals (Basel, Switzerland) (2023)
Cancer is a complex and heterogeneous disease and is still one of the leading causes of morbidity and mortality worldwide, mostly as the population ages. Despite the encouraging advances made over the years in chemotherapy, the development of new compounds for cancer treatments is an urgent priority. In recent years, the design and chemical synthesis of several innovative hybrid molecules, which bring different pharmacophores on the same scaffold, have attracted the interest of many researchers. Following this strategy, we designed and synthetized a series of new hybrid compounds that contain three pharmacophores, namely trimethoxybenzene, thiazolidinedione and thiazole, and tested their anticancer properties on two breast cancer (MCF-7 and MDA-MB-231) cell lines and one melanoma (A2058) cell line. The most active compounds were particularly effective against the MCF-7 cells and did not affect the viability of the normal MCF-10A cells. Docking simulations indicated the human Topoisomerases I and II (hTopos I and II) as possible targets of these compounds, the inhibitory activity of which was demonstrated by the mean of direct enzymatic assays. Particularly, compound 7e was proved to inhibit both the hTopo I and II, whereas compounds 7c,d blocked only the hTopo II. Finally, compound 7e was responsible for MCF-7 cell death by apoptosis. The reported results are promising for the further design and synthesis of other analogues potentially active as anticancer tools.
Keyphrases
- cell cycle arrest
- cell death
- breast cancer cells
- induced apoptosis
- endothelial cells
- pi k akt
- papillary thyroid
- endoplasmic reticulum stress
- molecular dynamics
- oxidative stress
- squamous cell
- high throughput
- molecular dynamics simulations
- hydrogen peroxide
- signaling pathway
- childhood cancer
- nitric oxide
- young adults
- single cell