The Mechanistic Roles of ncRNAs in Promoting and Supporting Chemoresistance of Colorectal Cancer

被引:24
作者
Micallef, Isaac [1 ]
Baron, Byron [1 ]
机构
[1] Univ Malta, Ctr Mol Med & Biobanking, MSD-2080 Msida, Malta
关键词
ncRNAs; miRNAs; lncRNAs; circRNAs; colorectal cancer; chemoresistance; 5-fluorouracil; oxaliplatin; cisplatin; doxorubicin; LONG NONCODING RNAS; EPITHELIAL-MESENCHYMAL TRANSITION; HUMAN COLON-CANCER; NF-KAPPA-B; DRUG-RESISTANCE; 5-FLUOROURACIL RESISTANCE; OXALIPLATIN RESISTANCE; CIRCULAR RNAS; CHEMOTHERAPY RESISTANCE; EPIGENETIC REGULATION;
D O I
10.3390/ncrna7020024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Colorectal Cancer (CRC) is one of the most common gastrointestinal malignancies which has quite a high mortality rate. Despite the advances made in CRC treatment, effective therapy is still quite challenging, particularly due to resistance arising throughout the treatment regimen. Several studies have been carried out to identify CRC chemoresistance mechanisms, with research showing different signalling pathways, certain ATP binding cassette (ABC) transporters and epithelial mesenchymal transition (EMT), among others to be responsible for the failure of CRC chemotherapies. In the last decade, it has become increasingly evident that certain non-coding RNA (ncRNA) families are involved in chemoresistance. Research investigations have demonstrated that dysregulation of microRNAs (miRNAs), long non-coding RNAs (lncRNAs) and circular RNAs (circRNAs) contribute towards promoting resistance in CRC via different mechanisms. Considering the currently available data on this phenomenon, a better understanding of how these ncRNAs participate in chemoresistance can lead to suitable solutions to overcome this problem in CRC. This review will first focus on discussing the different mechanisms of CRC resistance identified so far. The focus will then shift onto the roles of miRNAs, lncRNAs and circRNAs in promoting 5-fluorouracil (5-FU), oxaliplatin (OXA), cisplatin and doxorubicin (DOX) resistance in CRC, specifically using ncRNAs which have been recently identified and validated under in vivo or in vitro conditions.
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