Ong, Hien Thi My Ates, Eda Kwon, Oh-Seung Kang, Min-Jung 2024-01-19T08:04:29Z 2024-01-19T08:04:29Z 2023-12-21 2023-11 1480-9222 https://pubs.kist.re.kr/handle/201004/113102 BackgroundRenal cancer therapies are challenging owing to the extensive spreading of this cancer to other organs and its ability to pose resistance to current medications. Therefore, drugs targeting novel targets are urgently required to overcome these challenges. The cholesterol side-chain cleavage enzyme (CYP11A1) is closely associated with steroidogenesis, and its downregulation is linked to adrenal dysfunction and several types of carcinoma. We previously found that overexpression of CYP11A1 inhibited epithelial-mesenchymal transition and induced G2/M arrest in the kidney cancer Caki-1 cell line. In this context, natural compounds that exhibit potent CYP11A1 stimulation activity can be promising therpaeutic agents for kidney cancer.MethodsWe screened a panel of 1374 natural compounds in a wound-healing assay using CYP11A1-transfected Caki-1 cells. Of these, 167 promising biologically active compounds that inhibited cancer cell migration by more than 75% were selected, and their half-maximal inhibitory concentrations (IC50) were determined. The IC50 of 159 compounds was determined and 38 compounds with IC50 values less than 50 mu M were selected for further analysis. Steroid hormones (cholesterol and pregnenolone) levels in cells treated with the selected compounds were quantitated using LC-MS/MS to determine their effect on CYP11A1 activity. Western blotting for CYP11A1, autophagy signaling proteins, and ferroptosis regulators were performed to ivestigate the mechanisms underlying the action of the selected compounds.ResultsWe screened five promising natural lead compounds that inhibited cancer cell proliferation after three screening steps. The IC50 of these compounds was determined to be between 5.9 and 14.6 mu M. These candidate compounds increased the expression of CYP11A1 and suppressed cholesterol levels while increasing pregnenolone levels, which is consistent with the activation of CYP11A1. Our results showed that CYP11A1 activation inhibited the migration of cancer cells, promoted ferroptosis, and triggered autophagy signaling.ConclusionsThis study indicates that the CYP11A1-overexpressing Caki-1 cell line is useful for screening drugs against kidney cancer. The two selected compounds could be utilized as lead compounds for anticancer drug discovery, and specifically for the development of antirenal cancer medication. English BioMed Central Screening of Natural Compounds for CYP11A1 Stimulation Against Cell Renal Cell Carcinoma Article 10.1186/s12575-023-00225-y 1 Biological Procedures Online, v.25, no.1 Biological Procedures Online 25 1 Y scie scopus 001111416700001 2-s2.0-85178195328 Biochemical Research Methods Biochemistry & Molecular Biology Article DEATH PATHOGENESIS FERROPTOSIS INHIBITORS THERAPY Quantitative analysis of cholesterol and pregnenolone LC-MS/MS Autophagy Ferroptosis