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      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 16, Issue 4
      • مشاهده مورد
      •   صفحهٔ اصلی
      • نشریات انگلیسی
      • Iranian Journal of Pharmaceutical Research
      • Volume 16, Issue 4
      • مشاهده مورد
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      Anti-invasion Effects of Cannabinoids Agonist and Antagonist on Human Breast Cancer Stem Cells

      (ندگان)پدیدآور
      mohammad pour, fatemehOstad, Seyed NasserAliebrahimi, ShimaDaman, Zahra
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      اندازه فایل: 
      735.4کیلوبایت
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      نوع مدرک
      Text
      Research article
      زبان مدرک
      English
      نمایش کامل رکورد
      چکیده
      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
      AM251
      Breast cancer stem cell
      ACEA
      MDA-MB-231
      Invasion
      Cannabinoids
      toxicology and Pharmacology

      شماره نشریه
      4
      تاریخ نشر
      2017-11-01
      1396-08-10
      ناشر
      School of Pharmacy, Shahid Beheshti University of Medical Sciences
      سازمان پدید آورنده
      Department of Toxicology and Pharmacology, Faculty of Pharmacy and Poisoning Research Center, Tehran University of Medical Sciences, Tehran, Iran
      Department 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
      1735-0328
      1726-6890
      URI
      https://dx.doi.org/10.22037/ijpr.2017.2143
      http://ijpr.sbmu.ac.ir/article_2143.html
      https://iranjournals.nlai.ir/handle/123456789/313628

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