dc.contributor.author | MILLS, KINGSTON | en |
dc.contributor.author | CREAGH, EMMA | en |
dc.date.accessioned | 2015-12-09T11:50:26Z | |
dc.date.available | 2015-12-09T11:50:26Z | |
dc.date.issued | 2015 | en |
dc.date.submitted | 2015 | en |
dc.identifier.citation | Flood, B., Oficjalska, K., Laukens, D., Fay, J., Mills, K.H., Sheahan, K., Ryan, E.J., Doherty, G.A., Kay, E.W. and Creagh, E.M., Altered Expression of Caspases-4 and -5 during Inflammatory Bowel Disease and Colorectal Cancer - Novel Diagnostic and Therapeutic Potential., Clinical and Experimental Immunology, 181, 1, 2015, 39-50 | en |
dc.identifier.other | Y | en |
dc.description | PUBLISHED | en |
dc.description.abstract | Caspases are a group of proteolytic enzymes involved in the co-ordination
of cellular processes, including cellular homeostasis, inflammation and
apoptosis. Altered activity of caspases, particularly caspase-1, has been
implicated in the development of intestinal diseases, such as inflammatory
bowel disease (IBD) and colorectal cancer (CRC). However, the
involvement of two related inflammatory caspase members, caspases-4
and -5, during intestinal homeostasis and disease has not yet been
established. This study demonstrates that caspases-4 and -5 are involved
in IBD-associated intestinal inflammation. Furthermore, we found a clear
correlation between stromal caspase-4 and -5 expression levels,
inflammation and disease activity in ulcerative colitis patients.
Deregulated intestinal inflammation in IBD patients is associated with an
increased risk of developing CRC. We found robust expression of
caspases-4 and -5 within intestinal epithelial cells, exclusively within
neoplastic tissue, of colorectal tumours. An examination of adjacent
normal, inflamed and tumour tissue from patients with colitis-associated
CRC confirmed that stromal expression of caspases-4 and -5 is increased
in inflamed and dysplastic tissue, while epithelial expression is restricted
to neoplastic tissue. In addition to identifying caspases-4 and -5 as
potential targets for limiting intestinal inflammation, this study has
identified epithelial-expressed caspases-4 and -5 as biomarkers with
diagnostic and therapeutic potential in CRC. | en |
dc.description.sponsorship | This work was supported by grants from The Wellcome
Trust (grant no. 078306), the Broad Medical Research Pro-
gram (BMRP, no. IBD-0197) and Science Foundation Ire-
land (SFI, 12/IP/1400 | en |
dc.format.extent | 39-50 | en |
dc.language.iso | en | en |
dc.relation.ispartofseries | Clinical and Experimental Immunology | en |
dc.relation.ispartofseries | 181 | en |
dc.relation.ispartofseries | 1 | en |
dc.rights | Y | en |
dc.subject | caspases, colorectal cancer, inflammation, inflammatory bowel disease | en |
dc.subject.lcsh | caspases, colorectal cancer, inflammation, inflammatory bowel disease | en |
dc.title | Altered Expression of Caspases-4 and -5 during Inflammatory Bowel Disease and Colorectal Cancer - Novel Diagnostic and Therapeutic Potential. | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/ecreagh | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/millsk | en |
dc.identifier.rssinternalid | 101246 | en |
dc.identifier.doi | http://dx.doi.org/10.1111/cei.12617 | en |
dc.rights.ecaccessrights | openAccess | |
dc.subject.TCDTheme | Cancer | en |
dc.subject.TCDTheme | Immunology, Inflammation & Infection | en |
dc.subject.TCDTag | COLORECTAL CANCER | en |
dc.subject.TCDTag | Cancer Detection | en |
dc.subject.TCDTag | INFLAMMATORY BOWEL DISEASE | en |
dc.subject.TCDTag | Inflammation | en |
dc.contributor.sponsor | Higher Education Authority (HEA) | en |
dc.contributor.sponsorGrantNumber | scheme #201921, award # 12259 | en |
dc.contributor.sponsor | Wellcome Trust | en |
dc.contributor.sponsorGrantNumber | WT#078306 | en |
dc.contributor.sponsor | Science Foundation Ireland (SFI) | en |
dc.contributor.sponsorGrantNumber | SFI, 12/IP/1400 | en |
dc.identifier.uri | http://hdl.handle.net/2262/75183 | |