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      Apoptosis and cell cycle regulatory effects of adenosine by modulation of GLI‐1 and ERK1/2 pathways in CD44 + and CD24 breast cancer stem cells

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          Abstract

          Objectives

          Breast cancer stem cells ( CSCs) are a small population of tumour cells with the ability of self‐renewal and resistance to chemotherapy. Targeting CSCs is a promising strategy for treatment of cancer. A recent study demonstrated that adenosine receptor agonists inhibit glioblastoma CSCs proliferation. At present, the effect of adenosine on breast CSCs has not been reported. Therefore, this study was designed to evaluate the effect of adenosine and its signalling pathways in breast CSCs.

          Materials and methods

          Anti‐proliferative effect of adenosine on breast CSCs was evaluated by mammosphere formation and MTS assay. The effect of adenosine on cell cycle progression was examined using flow cytometry. Detection of apoptosis was conducted by Annexin V‐ FITC. The expression levels of cell cycle and apoptosis regulatory proteins as well as ERK1/2, and GLI‐1 were measured by Western blot.

          Results

          Adenosine reduced CSCs population and mammosphere formation in breast CSCs. Adenosine induced G1 cell cycle arrest in breast CSCs in conjunction with a marked down‐regulation of cyclin D1 and CDK4. Adenosine also induced apoptosis by regulation of Bax/Bcl‐2 ratio, mitochondrial membrane potential depletion and activation of caspase‐6. Moreover, adenosine inhibited ERK1/2 phosphorylation and GLI‐1 protein expression.

          Conclusions

          These findings indicated that adenosine induces cell cycle arrest and apoptosis through inhibition of GLI‐1 and ERK1/2 pathways in breast CSCs.

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          Author and article information

          Contributors
          maghaei@pharm.mui.ac.ir
          Journal
          Cell Prolif
          Cell Prolif
          10.1111/(ISSN)1365-2184
          CPR
          Cell Proliferation
          John Wiley and Sons Inc. (Hoboken )
          0960-7722
          1365-2184
          29 March 2017
          August 2017
          : 50
          : 4 ( doiID: 10.1111/cpr.2017.50.issue-4 )
          : e12345
          Affiliations
          [ 1 ] Department of Clinical Biochemistry School of Pharmacy and Pharmaceutical Sciences Isfahan University of Medical Sciences Isfahan Iran
          [ 2 ] Medical Laboratory Research Center Golestan University of Medical Sciences Gorgan Iran
          [ 3 ] Bioinformatics Research Center Isfahan University of Medical Sciences Isfahan Iran
          [ 4 ] Isfahan Pharmaceutical Sciences Research Center Isfahan University of Medical Sciences Isfahan Iran
          Author notes
          [*] [* ] Correspondence

          Mahmoud Aghaei, Department of Clinical Biochemistry, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.

          Email: maghaei@ 123456pharm.mui.ac.ir

          Author information
          http://orcid.org/0000-0002-1775-8761
          Article
          PMC6529124 PMC6529124 6529124 CPR12345
          10.1111/cpr.12345
          6529124
          28370734
          eeb245b5-4b72-4d21-bb18-69dd1ef3b697
          © 2017 John Wiley & Sons Ltd
          History
          : 07 November 2016
          : 07 February 2017
          Page count
          Figures: 7, Tables: 0, Pages: 12, Words: 6268
          Funding
          Funded by: Isfahan University of Medical Sciences
          Award ID: 9/907
          Funded by: golestan University of Medical Sciences
          Award ID: 35/246259
          Categories
          Original Article
          Original Articles
          Custom metadata
          2.0
          cpr12345
          August 2017
          Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.2.1 mode:remove_FC converted:02.05.2019

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