Author/Authors :
Mohammadpour, Fatemeh Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran , Ostad, Nasser Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran , Aliebrahimi, Shima Department of Cellular and Molecular Biology - School of Biology - College of Science - University of Tehran, Tehran, Iran , Daman, Zahra Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Studies show that cancer cell invasion or metastasis is the primary cause of death in
malignancies including breast cancer. The existence of cancer stem cells (CSCs) in breast cancer
may account for tumor initiation, progression, and metastasis. Recent studies have reported
different effects of cannabinoids on cancer cells via CB1 and CB2 cannabinoid receptors. In the
present study, the effects of ACEA (a selective CB1 receptor agonist) and AM251 (a selective
CB1 antagonist) on CSCs and their parental cells were investigated. Breast CSCs derived from
MDA-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 reduced
invasion and cytotoxic effects of the drug. Since one of the main cancer recurrence factors is
anti-cancer drugs fail to inhibit CSC population, this observation would be useful for cancer
treatment.
Keywords :
Cannabinoids , Invasion , MDA-MB-231 , ACEA , Breast cancer stem cell , AM251
