Cell adhesion molecules are altered during irinotecan-induced mucositis: a qualitative histopathological study
- PMID: 27650103
- DOI: 10.1007/s00520-016-3413-x
Cell adhesion molecules are altered during irinotecan-induced mucositis: a qualitative histopathological study
Abstract
Purpose: Chemotherapy-induced mucositis is characterised by damage to mucous membranes throughout the alimentary tract. This study aims to investigate the expression of cell adhesion molecules (CAMs) following treatment with irinotecan.
Methods: Dark agouti rats received a single dose of 175 mg/kg irinotecan and sacrificed at various time points after treatment. Picro-sirius red staining indicated an increase in collagen around crypts from 24 h in both small and large intestinal regions and this diminished at the later time points. CAMs E-cadherin, P-selectin, E-selectin and integrin-α1 were examined using immunohistochemistry.
Results: E-cadherin was significantly elevated in jejunal crypts at the time of maximal tissue damage (48 h), while it decreased at the healing phase (96 h) in both jejunum and colon. P-selectin expression decreased significantly in the jejunum following irinotecan. Crypt expression of E-selectin was significantly elevated in the healing phase of mucositis (96 h). Integrin-α1 expression was significantly altered during the time course in the villus (p = 0.0032) and lamina propria (p = 0.039).
Conclusions: Irinotecan induced a significant alteration in CAM expression in the jejunum and colon. Changes in adhesion molecule expression may have a direct impact on the loss of mucosal layer integrity seen in mucositis.
Keywords: Adhesion proteins; Alimentary tract; Chemotherapy; Histopathology; Mucositis.
Similar articles
-
Characterisation of mucosal changes in the alimentary tract following administration of irinotecan: implications for the pathobiology of mucositis.Cancer Chemother Pharmacol. 2008 Jun;62(1):33-41. doi: 10.1007/s00280-007-0570-0. Epub 2007 Aug 17. Cancer Chemother Pharmacol. 2008. PMID: 17703303
-
Matrix metalloproteinases are possible mediators for the development of alimentary tract mucositis in the dark agouti rat.Exp Biol Med (Maywood). 2010 Oct;235(10):1244-56. doi: 10.1258/ebm.2010.010082. Epub 2010 Aug 3. Exp Biol Med (Maywood). 2010. PMID: 20682600
-
Irinotecan-induced alterations in intestinal cell kinetics and extracellular matrix component expression in the Dark Agouti rat.Int J Exp Pathol. 2011 Oct;92(5):357-65. doi: 10.1111/j.1365-2613.2011.00771.x. Epub 2011 Apr 5. Int J Exp Pathol. 2011. PMID: 21463374 Free PMC article.
-
Irinotecan- and 5-fluorouracil-induced intestinal mucositis: insights into pathogenesis and therapeutic perspectives.Cancer Chemother Pharmacol. 2016 Nov;78(5):881-893. doi: 10.1007/s00280-016-3139-y. Epub 2016 Sep 2. Cancer Chemother Pharmacol. 2016. PMID: 27590709 Review.
-
Dark Agouti rat model of chemotherapy-induced mucositis: establishment and current state of the art.Exp Biol Med (Maywood). 2015 Jun;240(6):725-41. doi: 10.1177/1535370215581309. Epub 2015 May 12. Exp Biol Med (Maywood). 2015. PMID: 25966981 Free PMC article. Review.
Cited by
-
Restore intestinal steady-state: new advances in the clinical management of chemotherapy-associated diarrhea and constipation.J Mol Histol. 2025 Mar 8;56(2):101. doi: 10.1007/s10735-025-10367-w. J Mol Histol. 2025. PMID: 40056250 Free PMC article. Review.
-
Bioactive Polyphenols from Pomegranate Juice Reduce 5-Fluorouracil-Induced Intestinal Mucositis in Intestinal Epithelial Cells.Antioxidants (Basel). 2020 Aug 3;9(8):699. doi: 10.3390/antiox9080699. Antioxidants (Basel). 2020. PMID: 32756489 Free PMC article.
-
Gliclazide Prevents 5-FU-Induced Oral Mucositis by Reducing Oxidative Stress, Inflammation, and P-Selectin Adhesion Molecules.Front Physiol. 2019 Mar 26;10:327. doi: 10.3389/fphys.2019.00327. eCollection 2019. Front Physiol. 2019. PMID: 30971955 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources