High-Throughput Sequencing of miRNAs Reveals a Tissue Signature in Gastric Cancer and Suggests Novel Potential Biomarkers

被引:25
|
作者
Darnet, Sylvain [1 ]
Moreira, Fabiano C. [1 ,2 ]
Hamoy, Igor G. [1 ,3 ]
Burbano, Rommel [1 ,4 ]
Khayat, Andre [1 ,4 ]
Cruz, Aline [1 ]
Magalhaes, Leandro [1 ]
Silva, Artur [1 ]
Santos, Sidney [1 ,4 ]
Demachki, Samia [4 ,5 ]
Assumpcao, Monica [1 ,6 ]
Assumpcao, Paulo [4 ,6 ]
Ribeiro-dos-Santos, Andrea [1 ,4 ]
机构
[1] Fed Univ Para, Inst Ciencias Biol, BR-66059 Belem, Para, Brazil
[2] Ctr Univ Para, Area Ciencias Exatas & Tecnol, Belem, Para, Brazil
[3] Univ Fed Rural Amazonia, Belem, PA, Brazil
[4] Fed Univ Para, Nucleo Pesquisa Oncol, BR-66059 Belem, Para, Brazil
[5] Fed Univ Para, Inst Ciencias Saude, BR-66059 Belem, Para, Brazil
[6] Fed Univ Para, Hosp Univ Joao de Barros Barreto, BR-66059 Belem, Para, Brazil
来源
关键词
gastric cancer; miRnome; biomarkers; NGS;
D O I
10.4137/BBI.S23773
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Gastric cancer has a high incidence and mortality rate worldwide; however, the use of biomarkers for its clinical diagnosis remains limited. The microRNAs (miRNAs) are biomarkers with the potential to identify the risk and prognosis as well as therapeutic targets. We performed the ultradeep miRnomes sequencing of gastric adenocarcinoma and gastric antrum without tumor samples. We observed that a small set of those samples were responsible for approximately 80% of the total miRNAs expression, which might represent a miRNA tissue signature. Additionally, we identified seven miRNAs exhibiting significant differences, and, of these, hsa-miR-135b and hsa-miR-29c were able to discriminate antrum without tumor from gastric cancer regardless of the histological type. These findings were validated by quantitative real-time polymerase chain reaction. The results revealed that hsa-miR-135b and hsa-miR-29c are potential gastric adenocarcinoma occurrence biomarkers with the ability to identify individuals at a higher risk of developing this cancer, and could even be used as therapeutic targets to allow individualized clinical management.
引用
收藏
页码:1 / 8
页数:8
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