Mahinfar Parvaneh, Mansoori Behnaz, Rostamzadeh Davoud, Baradaran Behzad, Cho William C, Mansoori Behzad
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz 5166/15731, Iran.
Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran 175-14115, Iran.
Cancers (Basel). 2022 Jun 30;14(13):3217. doi: 10.3390/cancers14133217.
Glioblastoma (GBM) is an aggressive brain tumor that develops from neuroglial stem cells and represents a highly heterogeneous group of neoplasms. These tumors are predominantly correlated with a dismal prognosis and poor quality of life. In spite of major advances in developing novel and effective therapeutic strategies for patients with glioblastoma, multidrug resistance (MDR) is considered to be the major reason for treatment failure. Several mechanisms contribute to MDR in GBM, including upregulation of MDR transporters, alterations in the metabolism of drugs, dysregulation of apoptosis, defects in DNA repair, cancer stem cells, and epithelial-mesenchymal transition. MicroRNAs (miRNAs) are a large class of endogenous RNAs that participate in various cell events, including the mechanisms causing MDR in glioblastoma. In this review, we discuss the role of miRNAs in the regulation of the underlying mechanisms in MDR glioblastoma which will open up new avenues of inquiry for the treatment of glioblastoma.
胶质母细胞瘤(GBM)是一种侵袭性脑肿瘤,由神经胶质干细胞发展而来,是一组高度异质性的肿瘤。这些肿瘤主要与预后不良和生活质量差相关。尽管在为胶质母细胞瘤患者开发新颖有效的治疗策略方面取得了重大进展,但多药耐药(MDR)被认为是治疗失败的主要原因。GBM中导致MDR的机制有多种,包括MDR转运蛋白上调、药物代谢改变、细胞凋亡失调、DNA修复缺陷、癌症干细胞以及上皮-间质转化。微小RNA(miRNA)是一大类内源性RNA,参与各种细胞事件,包括导致胶质母细胞瘤MDR的机制。在本综述中,我们讨论了miRNA在调节MDR胶质母细胞瘤潜在机制中的作用,这将为胶质母细胞瘤的治疗开辟新的研究途径。