Anti-invasion Effects of Cannabinoids Agonist and Antagonist on Human Breast Cancer Stem Cells
(ندگان)پدیدآور
mohammad pour, fatemehOstad, Seyed NasserAliebrahimi, ShimaDaman, Zahraنوع مدرک
TextResearch article
زبان مدرک
Englishچکیده
Studies show that cancer cell invasion or metastasis is the primary cause of death inmalignancies including breast cancer. The existence of cancer stem cells (CSCs) in breast cancermay account for tumor initiation, progression, and metastasis. Recent studies have reporteddifferent effects of cannabinoids on cancer cells via CB1 and CB2 cannabinoid receptors. In thepresent study, the effects of ACEA (a selective CB1 receptor agonist) and AM251 (a selectiveCB1 antagonist) on CSCs and their parental cells were investigated. Breast CSCs derived fromMDA-MB-231 cell line were sorted and characterized with CD44+/CD24-/low/ESA+ phenotype.It was observed that ACEA decreased CD44+/CD24-/low/ESA+ cancer stem cell invasiveness.Conversely, AM251 increased the invasion by more than 20% (at the highest concentrations)in both MDA-MB-231 and CSCs. Our results did not show any correlation between reducedinvasion and cytotoxic effects of the drug. Since one of the main cancer recurrence factors isanti-cancer drugs fail to inhibit CSC population, this observation would be useful for cancertreatment.
کلید واژگان
AM251Breast cancer stem cell
ACEA
MDA-MB-231
Invasion
Cannabinoids
toxicology and Pharmacology
شماره نشریه
4تاریخ نشر
2017-11-011396-08-10
ناشر
School of Pharmacy, Shahid Beheshti University of Medical Sciencesسازمان پدید آورنده
Department of Toxicology and Pharmacology, Faculty of Pharmacy and Poisoning Research Center, Tehran University of Medical Sciences, Tehran, IranDepartment of Toxicology and Pharmacology, Faculty of Pharmacy and Poisoning Research Center, Tehran University of Medical Sciences, Tehran, Iran
Department of Cellular and Molecular Biology, School of Biology, College of Science, University of Tehran, Tehran, Iran.
Department of Toxicology and Pharmacology, Faculty of Pharmacy and Poisoning Research Center, Tehran University of Medical Sciences, Tehran, Iran.
شاپا
1735-03281726-6890




