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Emerging Roles of Exosomal Mirnas in Breast Cancer Drug Resistance Publisher Pubmed



Najminejad H1 ; Kalantar SM2 ; Abdollahpouralitappeh M3 ; Karimi MH4 ; Seifalian AM5 ; Gholipourmalekabadi M6, 7 ; Sheikhha MH2
Authors
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Authors Affiliations
  1. 1. Department of Medical Genetics, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
  2. 2. Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
  3. 3. Cellular and Molecular Biology Research Center, Larestan University of Medical Sciences, Larestan, Iran
  4. 4. Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  5. 5. Nanotechnology & Regenerative Medicine Commercialization Centre (Ltd), The London BioScience Innovation Centre, London, United Kingdom
  6. 6. Cellular and Molecular Research Centre, Iran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Tissue Engineering & Regenerative Medicine, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran

Source: IUBMB Life Published:2019


Abstract

Breast cancer (BC), as a heterogeneous disease, is considered as one of the most common malignancies in women worldwide. The resistance of BC cells to therapeutic agents has remained a big challenge in the treatment of BC patients. Some factors such as cytokines, exosomes, and soluble receptors were recognized as crucial agents involved in the development of drug resistance. However, the exact mechanisms underlying the drug resistance is still unknown. There is growing evidence to support the emerging roles of exosomes, especially exosomal miRNAs, in tumor initiation, angiogenesis, proliferation, migration, invasion, metastasis, and drug resistance. Therefore, identification of BC-specific exosomal miRNAs and their underlying mechanisms would be helpful to define sensitivity to therapeutic drugs and establish an appropriate therapeutic strategy. This review focuses mainly on the roles of exosomal miRNAs and their associated mechanisms in the resistance of BC cells to therapeutic agents, as well as critically examines the potential of these macromolecules as a treatment biomarker in BC patients. © 2019 International Union of Biochemistry and Molecular Biology
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