Molecular Effects of Targeting Multidrug Resistance of Doxorubicin Treated Breast Cancer Cells Using the Calcium Channel Blocker Nimodipine

Document Type : Original Article

Authors

1 Molecular Biology Department, Genetic Engineering and Biotechnology Institute, University of Sadat City, Sadat City, Egypt

2 Medical Laboratory Department, Faculty of Applied Medical Sciences, October 6 University, Cairo, Egypt

Abstract

Background/Aim: Multidrug resistance (MDR) is the leading cause of treatment failure in breast cancer patients treated with doxorubicin DOX). Previous indicated that some calcium channel blockers could reverse multidrug resistance. Therefore, we aimed to investigate the potential of nimodipine (a calcium channel blocker drug) in sensitizing breast cancer cells to DOX and elucidate the underlying molecular mechanisms. Methods: we examined the effects of DOX alone or in combination with nimodipine (NMD) on the viability of the MCF-7 cells using MTT assay, cell cycle by flow cytometry, and the expression of the MDR‐related gene (MDR1) and cell cycle/survival gene (Bcl‐2) and the pro-apoptotic gene (Bax) by quantitative reverse transcription polymerase chain reaction. Results: we found that adding NMD to DOX potentiated its antiproliferation effect. The value of the combination index (CI) of NMD/DOX was less than 1 indicating a synergistic effect. Combined DOX/NMD treatment also caused G1 arrest and potentiated apoptosis more than DOX‐single treatment. At the molecular levels, NMD/DOX treatment downregulated the mRNA of MDR1 and Bcl‐2; while upregulated the Bax gene compared with DOX alone. Conclusion: the results confirmed the potential of NMD in sensitizing Breast cancer to DOX by targeting MDR1 and suppressing the Bcl‐2 gene while upregulating the Bax gene. Additionally, NMD could be repurposed to reduce the therapeutic doses of DOX as indicated by the dose reduction index (DRI) and subsequently decrease its side effects (especially cardiotoxicity), along with decreasing the chemoresistance of breast cancer cells to DOX treatment.

Keywords

Main Subjects

Egyptian Journal of Chemistry
Volume 65, Issue 132 - Serial Number 13
Special Issue: Chemistry and Global Challenges (Part B)
December 2022
Pages 1053-1060

Files

Cited by

History

  • Receive Date: 11 August 2022
  • Revise Date: 28 August 2022
  • Accept Date: 31 August 2022

Share

How to cite

Statistics