Functional roles of exosomal miRNAs in multi-drug resistance in cancer chemotherapeutics

被引:9
作者
Mowla, Mahshid [1 ]
Hashemi, Atieh [1 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Tehran, Iran
关键词
Multidrug resistance; Exosome; microRNA; exomiR; Chemotherapy;
D O I
10.1016/j.yexmp.2020.104592
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Recent understanding of different molecular aspects of tumor initiation and progression has led to the discovery of a growing list of drugs. While these drugs have shown promising effects on tumor cells, their widespread usage has been hampered by the acquisition of drug resistance in a subpopulation of tumor cells. A differential pattern in the secretion of specialized vesicles named "exosomes" in drug-resistant cancer cells have recently received much attention. In addition, microRNAs (miRNAs) have been shown to be enriched in exosomes. Exosomal miRNAs (also known as exo-miRs) could be shuttled to recipient cells and play a role in the regulation of post-transcriptional gene expression, which may exert certain effects on cancer drug resistance. Here, we have reviewed the role of exo-miRs in chemotherapeutic resistance in different cancer types. Besides, studies which have focused on predictive role of circulating exo-miRs in cancer drug resistance are reviewed.
引用
收藏
页数:11
相关论文
共 134 条
[101]  
WALLACE JH, 1984, S AFR J SCI, V80, P203
[102]  
Wang, 2015, AC SC GYNECOL ONCOL, DOI [10.1016/j.ygyno.2015.11.034, DOI 10.1016/J.YGYNO.2015.11.034]
[103]  
WANG AZ, 2019, INT J BIOCHEM CELL B, DOI DOI 10.1016/j.biocel.2019.01.020
[104]   Exosomes derived from gemcitabine-resistant cells transfer malignant phenotypic traits via delivery of miRNA-222-3p [J].
Wei, Feng ;
Ma, Chengyuan ;
Zhou, Tong ;
Dong, Xuechao ;
Luo, Qinghua ;
Geng, Li ;
Ding, Lijuan ;
Zhang, Yandong ;
Zhang, Li ;
Li, Nan ;
Li, Yang ;
Liu, Yan .
MOLECULAR CANCER, 2017, 16
[105]   Overexpression of the microRNA miR-433 promotes resistance to paclitaxel through the induction of cellular senescence in ovarian cancer cells [J].
Weiner-Gorzel, Karolina ;
Dempsey, Eugene ;
Milewska, Malgorzata ;
McGoldrick, Aloysius ;
Toh, Valerie ;
Walsh, Aoibheann ;
Lindsay, Sinead ;
Gubbins, Luke ;
Cannon, Aoife ;
Sharpe, Daniel ;
O'Sullivan, Jacintha ;
Murphy, Madeline ;
Madden, Stephen F. ;
Kell, Malcolm ;
McCann, Amanda ;
Furlong, Fiona .
CANCER MEDICINE, 2015, 4 (05) :745-758
[106]   MiRNA-21 induces epithelial to mesenchymal transition and gemcitabine resistance via the PTEN/AKT pathway in breast cancer [J].
Wu, Zhen-Hua ;
Tao, Zhong-Hua ;
Zhang, Jian ;
Li, Ting ;
Ni, Chen ;
Xie, Jie ;
Zhang, Jin-Feng ;
Hu, Xi-Chun .
TUMOR BIOLOGY, 2016, 37 (06) :7245-7254
[107]  
WU ZT, 2016, EXOSOMES SMALL VESIC, V7, P60687, DOI DOI 10.18632/oncotarget.10807
[108]  
XIA HP, 2013, MICRORNA 216A 217 IN, V58, P629, DOI DOI 10.1002/hep.26369
[109]   Melanoma cell-derived exosomes promote epithelial-mesenchymal transition in primary melanocytes through paracrine/autocrine signaling in the tumor microenvironment [J].
Xiao, Deyi ;
Barry, Samantha ;
Kmetz, Daniel ;
Egger, Michael ;
Pan, Jianmin ;
Rai, Shesh N. ;
Qu, Jifu ;
McMasters, Kelly M. ;
Hao, Hongying .
CANCER LETTERS, 2016, 376 (02) :318-327
[110]   Exosomes: Decreased Sensitivity of Lung Cancer A549 Cells to Cisplatin [J].
Xiao, Xia ;
Yu, Shaorong ;
Li, Shuchun ;
Wu, Jianzhong ;
Ma, Rong ;
Cao, Haixia ;
Zhu, Yanliang ;
Feng, Jifeng .
PLOS ONE, 2014, 9 (02)