Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/33309
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorWang, F-
dc.creatorWong, SCC-
dc.creatorChan, LWC-
dc.creatorCho, WCS-
dc.creatorYip, SP-
dc.creatorYung, BYM-
dc.date.accessioned2014-12-30T08:38:28Z-
dc.date.available2014-12-30T08:38:28Z-
dc.identifier.issn2314-6133en_US
dc.identifier.urihttp://hdl.handle.net/10397/33309-
dc.language.isoenen_US
dc.publisherHindawi Publishing Corporationen_US
dc.rightsCopyright © 2014 Fengfeng Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following article: Wang, F., Wong, S. C., Chan, L. W., Cho, W., Yip, S. P., & Yung, B. Y. (2014). Multiple regression analysis of mRNA-miRNA associations in colorectal cancer pathway. BioMed research international, 2014, is available at https//doi.org/10.1155/2014/676724en_US
dc.titleMultiple regression analysis of mRNA-miRNA associations in colorectal cancer pathwayen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume2014en_US
dc.identifier.doi10.1155/2014/676724en_US
dcterms.abstractBackground. MicroRNA (miRNA) is a short and endogenous RNA molecule that regulates posttranscriptional gene expression. It is an important factor for tumorigenesis of colorectal cancer (CRC), and a potential biomarker for diagnosis, prognosis, and therapy of CRC. Our objective is to identify the related miRNAs and their associations with genes frequently involved in CRC microsatellite instability (MSI) and chromosomal instability (CIN) signaling pathways. Results. A regression model was adopted to identify the significantly associated miRNAs targeting a set of candidate genes frequently involved in colorectal cancer MSI and CIN pathways. Multiple linear regression analysis was used to construct the model and find the significant mRNA-miRNA associations. We identified three significantly associated mRNA-miRNA pairs: BCL2 was positively associated with miR-16 and SMAD4 was positively associated with miR-567 in the CRC tissue, while MSH6 was positively associated with miR-142-5p in the normal tissue. As for the whole model, BCL2 and SMAD4 models were not significant, and MSH6 model was significant. The significant associations were different in the normal and the CRC tissues. Conclusion. Our results have laid down a solid foundation in exploration of novel CRC mechanisms, and identification of miRNA roles as oncomirs or tumor suppressor mirs in CRC.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBioMed research international, 2014, v. 2014, 676724-
dcterms.isPartOfBioMed research international-
dcterms.issued2014-
dc.identifier.scopus2-s2.0-84901745369-
dc.identifier.pmid24895601-
dc.identifier.eissn2314-6141en_US
dc.identifier.rosgroupidr68867-
dc.description.ros2013-2014 > Academic research: refereed > Publication in refereed journalen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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