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- Publisher Website: 10.1136/gut.2008.167817
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- PMID: 19201770
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Article: Differential expression of microRNAs in plasma of patients with colorectal cancer: A potential marker for colorectal cancer screening
Title | Differential expression of microRNAs in plasma of patients with colorectal cancer: A potential marker for colorectal cancer screening | ||||||||||
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Authors | |||||||||||
Issue Date | 2009 | ||||||||||
Publisher | BMJ Publishing Group. The Journal's web site is located at http://gut.bmjjournals.com/ | ||||||||||
Citation | Gut, 2009, v. 58 n. 10, p. 1375-1381 How to Cite? | ||||||||||
Abstract | Objective: MicroRNAs (miRNAs) have been shown to offer great potential in the diagnosis of cancer. We investigated whether plasma miRNAs could discriminate between patients with and without colorectal cancer (CRC). Methods: This study was divided into three phases: (1) marker discovery using real-time PCR-based miRNA profiling on plasma, corresponding cancerous and adjacent non-cancerous colonic tissues of five patients with CRC, along with plasma from five healthy individuals as controls; (2) marker selection and validation by real-time quantitative RT-PCR on a small set of plasma; and (3) independent validation on a large set of plasma from 90 patients with CRC, 20 patients with gastric cancer, 20 patients with inflammatory bowel disease (IBD) and 50 healthy controls. Results: Of the panel of 95 miRNAs analysed, five were upregulated both in plasma and tissue samples. All the five miRNAs were validated on the plasma of 25 patients with CRC and 20 healthy controls. Both miR-17-3p and miR-92 were significantly elevated in the patients with CRC (p<0.0005). The plasma levels of these markers were significantly reduced after surgery in 10 patients with CRC (p<0.05). Further validation with an independent set of plasma samples (n=180) indicated that miR-92 differentiates CRC from gastric cancer, IBD and normal subjects. This marker yielded a receiver operating characteristic curve area of 88.5%. At a cut-off of 240 (relative expression in comparison to RNU6B snRNA), the sensitivity was 89% and the specificity was 70% in discriminating CRC from control subjects. Conclusion: MiR-92 is significantly elevated in plasma of patients with CRC and can be a potential non-invasive molecular marker for CRC screening. | ||||||||||
Persistent Identifier | http://hdl.handle.net/10722/92202 | ||||||||||
ISSN | 2023 Impact Factor: 23.0 2023 SCImago Journal Rankings: 8.052 | ||||||||||
ISI Accession Number ID |
Funding Information: The project was supported by the CUHK Direct Grant No. 2041342 and Research Funding from the Institute of Digestive Disease and the Li Ka Shing Institute of Health Science, the Chinese University of Hong Kong. | ||||||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ng, EKO | en_HK |
dc.contributor.author | Chong, WWS | en_HK |
dc.contributor.author | Jin, H | en_HK |
dc.contributor.author | Lam, EKY | en_HK |
dc.contributor.author | Shin, VY | en_HK |
dc.contributor.author | Yu, J | en_HK |
dc.contributor.author | Poon, TCW | en_HK |
dc.contributor.author | Ng, SSM | en_HK |
dc.contributor.author | Sung, JJY | en_HK |
dc.date.accessioned | 2010-09-17T10:39:05Z | - |
dc.date.available | 2010-09-17T10:39:05Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Gut, 2009, v. 58 n. 10, p. 1375-1381 | en_HK |
dc.identifier.issn | 0017-5749 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/92202 | - |
dc.description.abstract | Objective: MicroRNAs (miRNAs) have been shown to offer great potential in the diagnosis of cancer. We investigated whether plasma miRNAs could discriminate between patients with and without colorectal cancer (CRC). Methods: This study was divided into three phases: (1) marker discovery using real-time PCR-based miRNA profiling on plasma, corresponding cancerous and adjacent non-cancerous colonic tissues of five patients with CRC, along with plasma from five healthy individuals as controls; (2) marker selection and validation by real-time quantitative RT-PCR on a small set of plasma; and (3) independent validation on a large set of plasma from 90 patients with CRC, 20 patients with gastric cancer, 20 patients with inflammatory bowel disease (IBD) and 50 healthy controls. Results: Of the panel of 95 miRNAs analysed, five were upregulated both in plasma and tissue samples. All the five miRNAs were validated on the plasma of 25 patients with CRC and 20 healthy controls. Both miR-17-3p and miR-92 were significantly elevated in the patients with CRC (p<0.0005). The plasma levels of these markers were significantly reduced after surgery in 10 patients with CRC (p<0.05). Further validation with an independent set of plasma samples (n=180) indicated that miR-92 differentiates CRC from gastric cancer, IBD and normal subjects. This marker yielded a receiver operating characteristic curve area of 88.5%. At a cut-off of 240 (relative expression in comparison to RNU6B snRNA), the sensitivity was 89% and the specificity was 70% in discriminating CRC from control subjects. Conclusion: MiR-92 is significantly elevated in plasma of patients with CRC and can be a potential non-invasive molecular marker for CRC screening. | en_HK |
dc.language | eng | en_HK |
dc.publisher | BMJ Publishing Group. The Journal's web site is located at http://gut.bmjjournals.com/ | en_HK |
dc.relation.ispartof | Gut | en_HK |
dc.subject.mesh | Colorectal Neoplasms - diagnosis - genetics | - |
dc.subject.mesh | Gene Expression Regulation, Neoplastic - genetics | - |
dc.subject.mesh | MicroRNAs - genetics - metabolism | - |
dc.subject.mesh | Neoplastic Cells, Circulating - metabolism | - |
dc.subject.mesh | Tumor Markers, Biological - genetics - metabolism | - |
dc.title | Differential expression of microRNAs in plasma of patients with colorectal cancer: A potential marker for colorectal cancer screening | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0017-5749&volume=58&issue=10&spage=1375&epage=1381&date=2009&atitle=Differential+expression+of+microRNAs+in+plasma+of+patients+with+colorectal+cancer:+a+potential+marker+for+colorectal+cancer+screening | - |
dc.identifier.email | Ng, EKO: ngko@hku.hk | en_HK |
dc.identifier.authority | Ng, EKO=rp01364 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1136/gut.2008.167817 | en_HK |
dc.identifier.pmid | 19201770 | - |
dc.identifier.scopus | eid_2-s2.0-66049112674 | en_HK |
dc.identifier.hkuros | 168708 | - |
dc.identifier.hkuros | 194720 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-66049112674&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 58 | en_HK |
dc.identifier.issue | 10 | en_HK |
dc.identifier.spage | 1375 | en_HK |
dc.identifier.epage | 1381 | en_HK |
dc.identifier.isi | WOS:000269785500016 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Ng, EKO=21135553700 | en_HK |
dc.identifier.scopusauthorid | Chong, WWS=24576241300 | en_HK |
dc.identifier.scopusauthorid | Jin, H=24577511700 | en_HK |
dc.identifier.scopusauthorid | Lam, EKY=8644138600 | en_HK |
dc.identifier.scopusauthorid | Shin, VY=7003491170 | en_HK |
dc.identifier.scopusauthorid | Yu, J=35351306800 | en_HK |
dc.identifier.scopusauthorid | Poon, TCW=7006151710 | en_HK |
dc.identifier.scopusauthorid | Ng, SSM=26021413400 | en_HK |
dc.identifier.scopusauthorid | Sung, JJY=35405352400 | en_HK |
dc.identifier.citeulike | 4434628 | - |
dc.identifier.issnl | 0017-5749 | - |