TY - JOUR
T1 - NcRNAs
T2 - Multi-angle participation in the regulation of glioma chemotherapy resistance (Review)
AU - Zeng, Zhaomu
AU - Chen, Yueyue
AU - Geng, Xiuchao
AU - Zhang, Yuhao
AU - Wen, Xichao
AU - Yan, Qingyu
AU - Wang, Tingting
AU - Ling, Chen
AU - Xu, Yan
AU - Duan, Junchao
AU - Zheng, Kebin
AU - Sun, Zhiwei
N1 - Publisher Copyright:
© 2022 Spandidos Publications. All rights reserved.
PY - 2022/6
Y1 - 2022/6
N2 - As the most common primary tumour of the central nervous system, gliomas have a high recurrence rate after surgical resection and are resistant to chemotherapy, particularly high-grade gliomas dominated by glioblastoma multiforme (GBM). The prognosis of GBM remains poor despite improvements in treatment modalities, posing a serious threat to human health. At present, although drugs such as temozolomide, cisplatin and bevacizumab, are effective in improving the overall survival of patients with GBM, most patients eventually develop drug resistance, leading to poor clinical prognosis. The development of multidrug resistance has therefore become a major obstacle to improving the effectiveness of chemotherapy for GBM. The ability to fully understand the underlying mechanisms of chemotherapy resistance and to develop novel therapeutic targets to overcome resistance is critical to improving the prognosis of patients with GBM. Of note, growing evidence indicates that a large number of abnormally expressed noncoding RNAs (ncRNAs) have a central role in glioma chemoresistance and may target various mechanisms to modulate chemosensitivity. In the present review, the roles and molecular mechanisms of ncRNAs in glioma drug resistance were systematically summarized, the potential of ncRNAs as drug resistance markers and novel therapeutic targets of glioma were discussed and prospects for glioma treatment were outlined. ncRNAs are a research direction for tumor drug resistance mechanisms and targeted therapies, which not only provides novel perspectives for reversing glioma drug resistance but may also promote the development of precision medicine for clinical diagnosis and treatment.
AB - As the most common primary tumour of the central nervous system, gliomas have a high recurrence rate after surgical resection and are resistant to chemotherapy, particularly high-grade gliomas dominated by glioblastoma multiforme (GBM). The prognosis of GBM remains poor despite improvements in treatment modalities, posing a serious threat to human health. At present, although drugs such as temozolomide, cisplatin and bevacizumab, are effective in improving the overall survival of patients with GBM, most patients eventually develop drug resistance, leading to poor clinical prognosis. The development of multidrug resistance has therefore become a major obstacle to improving the effectiveness of chemotherapy for GBM. The ability to fully understand the underlying mechanisms of chemotherapy resistance and to develop novel therapeutic targets to overcome resistance is critical to improving the prognosis of patients with GBM. Of note, growing evidence indicates that a large number of abnormally expressed noncoding RNAs (ncRNAs) have a central role in glioma chemoresistance and may target various mechanisms to modulate chemosensitivity. In the present review, the roles and molecular mechanisms of ncRNAs in glioma drug resistance were systematically summarized, the potential of ncRNAs as drug resistance markers and novel therapeutic targets of glioma were discussed and prospects for glioma treatment were outlined. ncRNAs are a research direction for tumor drug resistance mechanisms and targeted therapies, which not only provides novel perspectives for reversing glioma drug resistance but may also promote the development of precision medicine for clinical diagnosis and treatment.
KW - chemoresistance
KW - circRNAs
KW - gliomas
KW - lncRNAs
KW - miRNAs
KW - nanomedicine
UR - http://www.scopus.com/inward/record.url?scp=85129997205&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85129997205&partnerID=8YFLogxK
U2 - 10.3892/ijo.2022.5366
DO - 10.3892/ijo.2022.5366
M3 - Review article
C2 - 35506469
AN - SCOPUS:85129997205
SN - 1019-6439
VL - 60
JO - International Journal of Oncology
JF - International Journal of Oncology
IS - 6
M1 - 5366
ER -