Please use this identifier to cite or link to this item:
https://doi.org/10.1186/1755-1536-3-11
DC Field | Value | |
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dc.title | Serum amyloid P ameliorates radiation-induced oral mucositis and fibrosis | |
dc.contributor.author | Murray, L.A | |
dc.contributor.author | Kramer, M.S | |
dc.contributor.author | Hesson, D.P | |
dc.contributor.author | Watkins, B.A | |
dc.contributor.author | Fey, E.G | |
dc.contributor.author | Argentieri, R.L | |
dc.contributor.author | Shaheen, F | |
dc.contributor.author | Knight, D.A | |
dc.contributor.author | Sonis, S.T | |
dc.date.accessioned | 2020-10-20T08:19:41Z | |
dc.date.available | 2020-10-20T08:19:41Z | |
dc.date.issued | 2010 | |
dc.identifier.citation | Murray, L.A, Kramer, M.S, Hesson, D.P, Watkins, B.A, Fey, E.G, Argentieri, R.L, Shaheen, F, Knight, D.A, Sonis, S.T (2010). Serum amyloid P ameliorates radiation-induced oral mucositis and fibrosis. Fibrogenesis and Tissue Repair 3 (1) : 11. ScholarBank@NUS Repository. https://doi.org/10.1186/1755-1536-3-11 | |
dc.identifier.issn | 1755-1536 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/178200 | |
dc.description.abstract | Purpose: To evaluate the effect of the anti-fibrotic protein serum amyloid P (SAP) on radiation-induced oral mucositis (OM) and fibrosis in a hamster cheek-pouch model.Experimental Design: Hamsters received a single dose of radiation (40 Gy) to the left everted cheek pouch to induce significant OM. The protective therapeutic potential of SAP was evaluated using varying dosing regimens. The extent of OM was measured using a validated six-point scoring scheme ranging from 0 (normal tissue, no mucositis) to 5 (complete ulceration). Fibrotic remodeling was also visualized histologically and quantified at later time points using collagen gene expression.Results: SAP treatment attenuated the profile of radiation-induced oral mucositis by delaying the time of onset, reducing the peak value, and enhancing the resolution of injury. The peak mucositis score was reduced by approximately 0.5 grade in SAP-treated animals. The number of animal days with a score of ? 3 was reduced by 48% in the SAP-treated group, compared with the saline control group (P < 0.01). SAP also inhibited the extent of tissue remodeling and decreased radiation-induced increases in myofibroblast number. Attenuated collagen deposition and gene expression was also observed in the cheek pouches of hamsters treated with SAP at both 16 and 28 days post-radiation.Conclusions: SAP treatment significantly attenuated radiation-induced injury. In particular, SAP attenuated the severity of OM and inhibited pathogenic remodeling. This suggests that SAP may be a useful therapy for the palliation of side effects observed during treatment for head and neck cancer. © 2010 Murray et al; licensee BioMed Central Ltd. | |
dc.publisher | BMC | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | serum amyloid P | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | animal tissue | |
dc.subject | article | |
dc.subject | cell proliferation | |
dc.subject | controlled study | |
dc.subject | disease severity | |
dc.subject | dose response | |
dc.subject | down regulation | |
dc.subject | epithelial mesenchymal transition | |
dc.subject | fibroblast | |
dc.subject | fibrogenesis | |
dc.subject | gene expression | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | immunohistochemistry | |
dc.subject | male | |
dc.subject | mouth disease | |
dc.subject | mucosa inflammation | |
dc.subject | myofibroblast | |
dc.subject | nonhuman | |
dc.subject | oral mucositis | |
dc.subject | radiation dose | |
dc.subject | radiation injury | |
dc.subject | tissue regeneration | |
dc.type | Article | |
dc.contributor.department | OBSTETRICS & GYNAECOLOGY | |
dc.description.doi | 10.1186/1755-1536-3-11 | |
dc.description.sourcetitle | Fibrogenesis and Tissue Repair | |
dc.description.volume | 3 | |
dc.description.issue | 1 | |
dc.description.page | 11 | |
dc.published.state | published | |
Appears in Collections: | Staff Publications Elements |
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