MicroRNAs as the pivotal regulators of Temozolomide resistance in glioblastoma

被引:4
作者
Yazdi, Mahsa Palizkaran [1 ]
Barjasteh, Amirhosein [2 ]
Moghbeli, Meysam [1 ]
机构
[1] Mashhad Univ Med Sci, Sch Med, Dept Med Genet & Mol Med, Mashhad, Iran
[2] Mashhad Univ Med Sci, Student Res Comm, Fac Med, Mashhad, Iran
关键词
Glioblastoma; Temozolomide; microRNA; Chemo resistance; Prognosis; GROWTH-FACTOR RECEPTOR; GLIOMA-CELLS; MALIGNANT GLIOMA; BETA-CATENIN; C-MET; SIGNALING PATHWAYS; MIR-125B INHIBITOR; DOWN-REGULATION; CANCER-CELLS; STEM-CELLS;
D O I
10.1186/s13041-024-01113-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glioblastoma (GBM) is an aggressive nervous system tumor with a poor prognosis. Although, surgery, radiation therapy, and chemotherapy are the current standard protocol for GBM patients, there is still a poor prognosis in these patients. Temozolomide (TMZ) as a first-line therapeutic agent in GBM can easily cross from the blood-brain barrier to inhibit tumor cell proliferation. However, there is a high rate of TMZ resistance in GBM patients. Since, there are limited therapeutic choices for GBM patients who develop TMZ resistance; it is required to clarify the molecular mechanisms of chemo resistance to introduce the novel therapeutic targets. MicroRNAs (miRNAs) regulate chemo resistance through regulation of drug metabolism, absorption, DNA repair, apoptosis, and cell cycle. In the present review we discussed the role of miRNAs in TMZ response of GBM cells. It has been reported that miRNAs mainly induced TMZ sensitivity by regulation of signaling pathways and autophagy in GBM cells. Therefore, miRNAs can be used as the reliable diagnostic/prognostic markers in GBM patients. They can also be used as the therapeutic targets to improve the TMZ response in GBM cells.
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页数:12
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