Cargando…

Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer

Background: The lack of screening methods with high diagnostic utility leads to colorectal cancer (CRC) patients usually diagnosed in advanced stages which results in high mortality. This study aimed to identify novel circulating miRNAs as biomarkers for the early detection of CRC. Materials and Met...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Xiangxiang, Xu, Xueni, Pan, Bei, He, Bangshun, Chen, Xiaoxiang, Zeng, Kaixuan, Xu, Mu, Pan, Yuqin, Sun, Huiling, Xu, Tao, Hu, Xiuxiu, Wang, Shukui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329864/
https://www.ncbi.nlm.nih.gov/pubmed/30662524
http://dx.doi.org/10.7150/jca.26723
_version_ 1783386885751570432
author Liu, Xiangxiang
Xu, Xueni
Pan, Bei
He, Bangshun
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
Pan, Yuqin
Sun, Huiling
Xu, Tao
Hu, Xiuxiu
Wang, Shukui
author_facet Liu, Xiangxiang
Xu, Xueni
Pan, Bei
He, Bangshun
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
Pan, Yuqin
Sun, Huiling
Xu, Tao
Hu, Xiuxiu
Wang, Shukui
author_sort Liu, Xiangxiang
collection PubMed
description Background: The lack of screening methods with high diagnostic utility leads to colorectal cancer (CRC) patients usually diagnosed in advanced stages which results in high mortality. This study aimed to identify novel circulating miRNAs as biomarkers for the early detection of CRC. Materials and Methods: Total 205 participants were enrolled in this study. First, two dysregulated candidate miRNAs were selected after integrated analysis of four GEO datasets. Then, the expression of these two miRNAs in plasma samples were tested through qRT-PCR. Training phase and validation phase were designed to verify the diagnostic value of these two miRNAs using receiver operating characteristic curve (ROC) analysis. Results: After integrated analysis of GEO datasets, we discovered miR-1290 and miR-320d were dysregulated in colorectal adenoma and adenocarcinoma tissues, and circulating miR-1290 and miR-320d in CRC patients were tumor-derived. Thereafter, circulating miR-1290 and miR-320d were selected to further investigate their potential for early diagnosis of CRC. Plasma miR-1290 expression could differentiate adenoma and CRC patients from healthy controls with area under the curve (AUC) of 0.78 and 0.88. Similarly, plasma miR-320d expression could discriminate adenoma and CRC patients from healthy controls with AUC of 0.74 and 0.81. Conclusions: Circulating miR-1290 and miR-320d are novel promising biomarkers for early diagnosis of CRC.
format Online
Article
Text
id pubmed-6329864
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-63298642019-01-18 Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer Liu, Xiangxiang Xu, Xueni Pan, Bei He, Bangshun Chen, Xiaoxiang Zeng, Kaixuan Xu, Mu Pan, Yuqin Sun, Huiling Xu, Tao Hu, Xiuxiu Wang, Shukui J Cancer Research Paper Background: The lack of screening methods with high diagnostic utility leads to colorectal cancer (CRC) patients usually diagnosed in advanced stages which results in high mortality. This study aimed to identify novel circulating miRNAs as biomarkers for the early detection of CRC. Materials and Methods: Total 205 participants were enrolled in this study. First, two dysregulated candidate miRNAs were selected after integrated analysis of four GEO datasets. Then, the expression of these two miRNAs in plasma samples were tested through qRT-PCR. Training phase and validation phase were designed to verify the diagnostic value of these two miRNAs using receiver operating characteristic curve (ROC) analysis. Results: After integrated analysis of GEO datasets, we discovered miR-1290 and miR-320d were dysregulated in colorectal adenoma and adenocarcinoma tissues, and circulating miR-1290 and miR-320d in CRC patients were tumor-derived. Thereafter, circulating miR-1290 and miR-320d were selected to further investigate their potential for early diagnosis of CRC. Plasma miR-1290 expression could differentiate adenoma and CRC patients from healthy controls with area under the curve (AUC) of 0.78 and 0.88. Similarly, plasma miR-320d expression could discriminate adenoma and CRC patients from healthy controls with AUC of 0.74 and 0.81. Conclusions: Circulating miR-1290 and miR-320d are novel promising biomarkers for early diagnosis of CRC. Ivyspring International Publisher 2019-01-01 /pmc/articles/PMC6329864/ /pubmed/30662524 http://dx.doi.org/10.7150/jca.26723 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Liu, Xiangxiang
Xu, Xueni
Pan, Bei
He, Bangshun
Chen, Xiaoxiang
Zeng, Kaixuan
Xu, Mu
Pan, Yuqin
Sun, Huiling
Xu, Tao
Hu, Xiuxiu
Wang, Shukui
Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title_full Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title_fullStr Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title_full_unstemmed Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title_short Circulating miR-1290 and miR-320d as Novel Diagnostic Biomarkers of Human Colorectal Cancer
title_sort circulating mir-1290 and mir-320d as novel diagnostic biomarkers of human colorectal cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329864/
https://www.ncbi.nlm.nih.gov/pubmed/30662524
http://dx.doi.org/10.7150/jca.26723
work_keys_str_mv AT liuxiangxiang circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT xuxueni circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT panbei circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT hebangshun circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT chenxiaoxiang circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT zengkaixuan circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT xumu circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT panyuqin circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT sunhuiling circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT xutao circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT huxiuxiu circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer
AT wangshukui circulatingmir1290andmir320dasnoveldiagnosticbiomarkersofhumancolorectalcancer