Urea-functionalized organoselenium compounds as promising anti-HepG2 and apoptosis-inducing agents

53Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Hepatocellular carcinoma is a highly aggressive and difficult-to-treat type of cancer. Incorporating urea functionality into the backbone of organoselenium compounds is expected to develop promising chemotherapeutic leads against liver cancer. Methods: Urea-functionalized organoselenium compounds were synthesized in good yields, and their cytotoxicity was evaluated against HepG2 cells. Results: 1,1′-(Diselanediylbis(4,1-phenylene))bis(3-phenylurea) (14) exhibited efficient anti-HepG2 activity in sub-micromolar concentrations, with no toxicity to normal human skin fibroblasts the molecular mechanisms of the diselenide-based urea 14 were evaluated using colony formation, wound healing, 3D spheroid invasion assays, cell cycle analysis and apoptosis induction. Its redox properties were also assessed by using different bioassays. Conclusion: Our study revealed promising anticancer, antimigratory and anti-invasiveness properties of 1,1′-(diselanediylbis(4,1-phenylene))bis(3-phenylurea) (14) against HepG2.

Cite

CITATION STYLE

APA

El-Senduny, F. F., Shabana, S. M., Rosel, D., Brabek, J., Althagafi, I., Angeloni, G., … Shaaban, S. (2021). Urea-functionalized organoselenium compounds as promising anti-HepG2 and apoptosis-inducing agents. Future Medicinal Chemistry, 13(19), 1655–1677. https://doi.org/10.4155/fmc-2021-0114

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free