The Effects of Curcumin-based Compounds on Proliferation and Cell Death in Cervical Cancer Cells.
Xiaojie Zhanga, Rubing Wanga, Guanglin Chena, Laurent M. Dejeana b, Qiao‐Hong Chena b
- aDepartment of Chemistry, California State University, Fresno, CA, U.S.A
- bDepartment of Chemistry, California State University, Fresno, CA, U.S.A. qchen@csufresno.edu ldejean@csufresno.edu
Papers open inside SciRah from the original publisher or repository; SciRah never hosts them.
Abstract
AIM: To systematically investigate the effects of a class of curcumin-based compounds on cancer cell viability, proliferation, and apoptosis. MATERIALS AND METHODS: Cytotoxicity and anti-proliferative potency were estimated by the trypan blue exclusion assay and WST-1 cell proliferation assay, respectively. Cell death pathways were discriminated according to plasma membrane integrity and lipid asymmetry cell profiles using a F2N12S and CYTOX AADvanced double staining flow cytometry-based assay. RESULTS: Nine compounds ( 2-10: ) exhibit 13- to 58-fold better cytotoxic and anti-proliferative potencies than curcumin towards HeLa cells. In this cervical cancer cell model, dienone and 1-methylpiperidone serve as the favorable central linkers; 5-methylisoxazol-3-yl and 3-methylisoxazol-5-yl act as the optimal terminal aromatic moiety. Finally, the effects of compounds 6: and 10: on HeLa cells' plasma membrane integrity and lipid asymmetry suggest that the early cytotoxic effect of these compounds is due to a stimulation of apoptosis.
TL;DRThe effects of compounds 6: and 10: on HeLa cells' plasma membrane integrity and lipid asymmetry suggest that the early cytotoxic effect of these compounds is due to a stimulation of apoptosis. (Semantic Scholar)