Int Electron J Med. 2020;9(1): 14-20.
doi: 10.34172/iejm.2020.03
  Abstract View: 181
  PDF Download: 116

Original Article

Adenosine A1 Receptor Antagonist Up-regulates Casp3 and Stimulates Apoptosis Rate in Breast Cancer Cell Line T47D

Mohammad Zamani Rarani 1,2 ORCID logo, Fahimeh Zamani Rarani 3 * ORCID logo, Ali Valiani 3, Zeinolabedin Shrifian Dastjerdi 1,2 ORCID logo, Elias Kargar Abargouei 1,2 ORCID logo, Ebrahim Eftekhar 1,2 ORCID logo, Asghar Taheri Kafran 4, Majid Pourentezari 5, Malihe Saghebray 1, Farnoosh Razavi 1, Sanaz Hadizadeh 1, Mehdi Nikbakht Dastjerdi 3

1 Department of Anatomical Sciences, Faculty of Medicine, Hormozgan University of Medical Sciences, Hormozgan, Iran.
2 Molecular Medicine Research Center, Hormozgan Health Institute, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
3 Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
4 Department of Biotechnology, Faculty of Advanced Sciences and Technologies, University of Isfahan, Isfahan, Iran.
5 Department of Biology and Anatomical Sciences, Medical School, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
*Correspondence to Fahimeh Zamani Rarani, Department of Anatomical Sciences, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. Tel: 00989103983026, E-mail: mz123esf@gmail. com


Background: Adenosine receptor family, especially A1 type is-overexpressed in breast-derived tumor cells and the P53 gene is mutant in some of these cells while the casps gene is of wild type as well. The aim of this study was to evaluate the effect of the A1 receptor function on cell programmed death or proliferation, as well as the relationship between this receptor stimulation/inhibition and caspase 3 (casp3) expression in T47D cell line that has a mutant and non-functional P53 gene.

Materials and Methods: The expression of casps3 was measured by real-time polymerase chain reaction and then flow cytometery and MTT assay were used to assess the apoptotic and proliferation cell rate after the treatment of T47D cells with specific agonist N6-cyclopentyladenosine (CPA) and antagonist 1,3-dipropyl-8-cyclopentylxanthine (DPCPX) of this receptor 24, 48, and 72 hours after treatment.

Result: Our results indicated that DPCPX significantly induces apoptosis in T47D cells and the rate of survival cell after the reduction of this treatment, especially 72 hours after treatment. Finally, the expression of casp3 was up-regulated by DPCPX treatment, especially in 72 hours while CPA treatment had opposite results (P>0.05).

Conclusion: In general, DPCPX could up-regulate casp3 gene expression and subsequently increase the apoptosis rate in T47D cells with casp3 expression without the P53 gene interference. Therefore, adenosine A1 receptor antagonists may be introduced as anti-cancer agents.

Keywords: Receptor, Adenosine A1, Apoptosis, Genes, Casp3, T47D Cells
First Name
Last Name
Email Address
Security code

Abstract View: 181

Your browser does not support the canvas element.

PDF Download: 116

Your browser does not support the canvas element.