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MicroRNA-mediated drug resistance in ovarian cancer.
Mihanfar, Aynaz; Fattahi, Amir; Nejabati, Hamid Reza.
Afiliação
  • Mihanfar A; Women's Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Fattahi A; Faculty of Medicine, Department of Biochemistry, Urmia University of Medical Sciences, Urmia, Iran.
  • Nejabati HR; Faculty of Advanced Medical Sciences, Department of Reproductive Biology, Tabriz University of Medical Sciences, Tabriz, Iran.
J Cell Physiol ; 234(4): 3180-3191, 2019 04.
Article em En | MEDLINE | ID: mdl-28628227
The development of intrinsic or acquired resistance to chemotherapeutic agents used in the treatment of various human cancers is a major obstacle for the successful abolishment of cancer. The accumulated efforts in the understanding the exact mechanisms of development of multidrug resistance (MDR) have led to the introduction of several unique and common mechanisms. Recent studies demonstrate the regulatory role of small noncoding RNA or miRNA in the several parts of cancer biology. Practically all aspects of cell physiology under normal and disease conditions are reported to be controlled by miRNAs. In this review, we discuss how the miRNA profile is changed upon MDR development and the pivotal regulatory role played by miRNAs in overcoming resistance to chemotherapeutic agents. It is hoped that further studies will support the use of these differentially expressed miRNAs as prognostic and predictive markers, as well as novel therapeutic targets to overcome resistance in ovarian cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / MicroRNAs / Antineoplásicos Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Resistência a Múltiplos Medicamentos / Resistencia a Medicamentos Antineoplásicos / MicroRNAs / Antineoplásicos Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article