Discovery of Novel miRNAs in Colorectal Cancer: Potential Biological Roles and Clinical Utility

被引:3
|
作者
Minutentag, Iael Weissberg [1 ,2 ]
Seneda, Ana Laura [1 ,2 ]
Barros-Filhos, Mateus C. [3 ]
de Carvalho, Marcio [4 ]
Souza, Vanessa G. P. [2 ,5 ]
Hasimoto, Claudia N. [1 ]
Moraes, Marcelo P. T. [1 ,6 ]
Marchi, Fabio A. [7 ,8 ]
Lam, Wan L. [9 ]
Reis, Patricia P. [1 ,2 ]
Drigo, Sandra A. [1 ,2 ]
机构
[1] Sao Paulo State Univ UNESP, Med Sch, Dept Surg & Orthoped, BR-18618687 Botucatu, Brazil
[2] Sao Paulo State Univ UNESP, Expt Res Unity UNIPEX, BR-18618687 Botucatu, Brazil
[3] A C Camargo Canc Ctr, Ctr Int Pesquisa CIPE, BR-01508010 Sao Paulo, Brazil
[4] Sao Paulo State Univ UNESP, Sch Vet Med & Anim Sci, BR-18618687 Botucatu, Brazil
[5] Sao Paulo State Univ UNESP, Inst Biosci, Dept Genet, BR-18618687 Botucatu, Brazil
[6] Sao Paulo State Univ UNESP, Med Sch, Dept Pathol, BR-18618687 Botucatu, Brazil
[7] Univ Sao Paulo, Med Sch, Dept Head & Neck Surg, BR-01246903 Sao Paulo, Brazil
[8] Univ Sao Paulo, Sao Paulo State Canc Inst ICESP, BR-01246903 Sao Paulo, Brazil
[9] British Columbia Canc Res Ctr, Vancouver, BC V5Z 1L3, Canada
关键词
colorectal cancer; tumor location; novel microRNA; miRMaster; tissue specificity; prognosis; small-RNAseq; TUMOR-SUPPRESSOR; FRAGILE SITES; MICRORNAS; LOCATION; COLON; GENE;
D O I
10.3390/ncrna9060065
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
Deregulated miRNAs are associated with colorectal cancer (CRC), with alterations depending on the tumor location. Novel tissue-specific miRNAs have been identified in different tumors and are associated with cancer. We used miRMaster to identify novel miRNAs in CRC from the TCGA and GEO data (discovery and validation groups). We used TCGA data from five tissues to analyze miRNA tissue specificity. miRDB was used to predict miRNA targets, and the UCSC Xena Browser was used to evaluate target expression. After successive analyses, we identified 15 novel miRNAs with the same expression patterns in CRC in both the discovery and validation groups. Four molecules (nov-miR-13844-5p, nov-miR-7154-5p, nov-miR-5035-3p, and nov-miR-590-5p) were differentially expressed in proximal and distal CRC. The nov-miR-3345-5p and nov-miR-13172-3p, which are upregulated in tumors, are only expressed in colorectal tissues. These molecules have been linked to a worse prognosis in right-sided colon and rectal carcinomas. An analysis revealed an association between eight novel miRNAs and 81 targets, mostly cancer-related genes, with varying expression based on tumor location. These findings provide new miRNAs with potential biological relevance, molecular biomarkers, and therapeutic targets for CRC treatment.
引用
收藏
页数:16
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