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- Publisher Website: 10.1136/gutjnl-2011-300178
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- PMID: 21813472
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Article: MicroRNA-375 inhibits tumour growth and metastasis in oesophageal squamous cell carcinoma through repressing insulin-like growth factor 1 receptor
Title | MicroRNA-375 inhibits tumour growth and metastasis in oesophageal squamous cell carcinoma through repressing insulin-like growth factor 1 receptor | ||||||||
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Authors | |||||||||
Issue Date | 2012 | ||||||||
Publisher | BMJ Publishing Group. The Journal's web site is located at http://gut.bmjjournals.com/ | ||||||||
Citation | Gut, 2012, v. 61 n. 1, p. 33-42 How to Cite? | ||||||||
Abstract | Background: To understand the involvement of micro- RNA (miRNA) in the development and progression of oesophageal squamous cell carcinoma (ESCC), miRNA profiles were compared between tumour and corresponding non-tumour tissues. Methods: miRCURY LNA array was used to generate miRNA expressing profile. Real-time quantitative PCR was applied to detectthe expression of miR-375 in ESCC samples and its correlation with insulin-like growth factor 1 receptor (IGF1R). Methylation-specific PCR was used to study the methylation status in the promoter region of miR-375. The tumour-suppressive effect of miR-375 was determined by both in-vitro and in-vivo assays. Results: The downregulation of miR-375 was frequently detected in primary ESCC, which was significantly correlated with advanced stage (p=0.003), distant metastasis (p<0.0001), poor overall survival (p=0.048) and disease-free survival (p=0.0006). Promoter methylation of miR-375 was detected in 26 of 45 (57.8%) ESCC specimens. Functional assays demonstrated that miR-375 could inhibit clonogenicity, cell motility, cell proliferation, tumour formation and metastasis in mice. Further study showed that miR-375 could interact with the 39-untranslated region of IGF1R and downregulate its expression. In clinical specimens, the expression of IGF1R was also negatively correlated with miR-375 expression (p=0.008). Conclusions: This study demonstrates that miR-375 has a strong tumour-suppressive effect through inhibiting the expression of IGF1R. The downregulation of miR-375, which is mainly caused by promoter methylation, is one of the molecular mechanisms involved in the development and progression of ESCC. | ||||||||
Persistent Identifier | http://hdl.handle.net/10722/144525 | ||||||||
ISSN | 2023 Impact Factor: 23.0 2023 SCImago Journal Rankings: 8.052 | ||||||||
ISI Accession Number ID |
Funding Information: This work was supported by grants from Hong Kong Research Grant Council Central Allocation (HKUST 2/06C); the National Natural Science Foundation of China (30700820, 30772475 and 30971606); and Sun Yat-Sen University 'Hundred Talents Program' (85000-3171311). | ||||||||
References | |||||||||
Grants |
DC Field | Value | Language |
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dc.contributor.author | Kong, KL | en_HK |
dc.contributor.author | Kwong, DLW | en_HK |
dc.contributor.author | Chan, THM | en_HK |
dc.contributor.author | Law, SYK | en_HK |
dc.contributor.author | Chen, L | en_HK |
dc.contributor.author | Li, Y | en_HK |
dc.contributor.author | Qin, YR | en_HK |
dc.contributor.author | Guan, XY | en_HK |
dc.date.accessioned | 2012-02-03T06:12:23Z | - |
dc.date.available | 2012-02-03T06:12:23Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Gut, 2012, v. 61 n. 1, p. 33-42 | en_HK |
dc.identifier.issn | 0017-5749 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/144525 | - |
dc.description.abstract | Background: To understand the involvement of micro- RNA (miRNA) in the development and progression of oesophageal squamous cell carcinoma (ESCC), miRNA profiles were compared between tumour and corresponding non-tumour tissues. Methods: miRCURY LNA array was used to generate miRNA expressing profile. Real-time quantitative PCR was applied to detectthe expression of miR-375 in ESCC samples and its correlation with insulin-like growth factor 1 receptor (IGF1R). Methylation-specific PCR was used to study the methylation status in the promoter region of miR-375. The tumour-suppressive effect of miR-375 was determined by both in-vitro and in-vivo assays. Results: The downregulation of miR-375 was frequently detected in primary ESCC, which was significantly correlated with advanced stage (p=0.003), distant metastasis (p<0.0001), poor overall survival (p=0.048) and disease-free survival (p=0.0006). Promoter methylation of miR-375 was detected in 26 of 45 (57.8%) ESCC specimens. Functional assays demonstrated that miR-375 could inhibit clonogenicity, cell motility, cell proliferation, tumour formation and metastasis in mice. Further study showed that miR-375 could interact with the 39-untranslated region of IGF1R and downregulate its expression. In clinical specimens, the expression of IGF1R was also negatively correlated with miR-375 expression (p=0.008). Conclusions: This study demonstrates that miR-375 has a strong tumour-suppressive effect through inhibiting the expression of IGF1R. The downregulation of miR-375, which is mainly caused by promoter methylation, is one of the molecular mechanisms involved in the development and progression of ESCC. | en_HK |
dc.language | eng | en_US |
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.rights | © 2011, Published by the BMJ Publishing Group Limited. | - |
dc.subject.mesh | Carcinoma, Squamous Cell - genetics - mortality - pathology | - |
dc.subject.mesh | Esophageal Neoplasms - genetics - mortality - pathology | - |
dc.subject.mesh | MicroRNAs - chemistry - metabolism | - |
dc.subject.mesh | Receptor, IGF Type 1 - metabolism | - |
dc.subject.mesh | Tumor Markers, Biological - chemistry - metabolism | - |
dc.title | MicroRNA-375 inhibits tumour growth and metastasis in oesophageal squamous cell carcinoma through repressing insulin-like growth factor 1 receptor | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Kwong, DLW: dlwkwong@hku.hk | en_HK |
dc.identifier.email | Law, SYK: slaw@hku.hk | en_HK |
dc.identifier.email | Guan, XY: xyguan@hkucc.hku.hk | en_HK |
dc.identifier.authority | Kwong, DLW=rp00414 | en_HK |
dc.identifier.authority | Law, SYK=rp00437 | en_HK |
dc.identifier.authority | Guan, XY=rp00454 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1136/gutjnl-2011-300178 | en_HK |
dc.identifier.pmid | 21813472 | - |
dc.identifier.scopus | eid_2-s2.0-83555177355 | en_HK |
dc.identifier.hkuros | 194831 | en_US |
dc.identifier.hkuros | 198359 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-83555177355&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 61 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 33 | en_HK |
dc.identifier.epage | 42 | en_HK |
dc.identifier.eissn | 1468-3288 | - |
dc.identifier.isi | WOS:000298179200005 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.f1000 | 13416965 | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.relation.project | Esophageal Carcinoma Research Center | - |
dc.identifier.scopusauthorid | Kong, KL=36106004300 | en_HK |
dc.identifier.scopusauthorid | Kwong, DLW=15744231600 | en_HK |
dc.identifier.scopusauthorid | Chan, THM=26431726400 | en_HK |
dc.identifier.scopusauthorid | Law, SYK=7202241293 | en_HK |
dc.identifier.scopusauthorid | Chen, L=23569135400 | en_HK |
dc.identifier.scopusauthorid | Li, Y=36078298200 | en_HK |
dc.identifier.scopusauthorid | Qin, YR=7403100680 | en_HK |
dc.identifier.scopusauthorid | Guan, XY=7201463221 | en_HK |
dc.identifier.issnl | 0017-5749 | - |