参考文献:1.Sonis ST (2004) The pathobiology of mucositis. Nat Rev Cancer 4(4):p. 277–p. 284CrossRef 2.Carlotto A et al. (2013) The economic burden of toxicities associated with cancer treatment: review of the literature and analysis of nausea and vomiting, diarrhoea, oral mucositis and fatigue. PharmacoEconomics 31(9):753–766CrossRef PubMed 3.Logan RM et al. (2008) Characterisation of mucosal changes in the alimentary tract following administration of irinotecan: implications for the pathobiology of mucositis. Cancer Chemother Pharmacol 62(1):33–41CrossRef PubMed 4.Keefe DM (2007) Intestinal mucositis: mechanisms and management. Curr Opin Oncol 19(4):323–327CrossRef PubMed 5.Keefe DM et al. (2000) Chemotherapy for cancer causes apoptosis that precedes hypoplasia in crypts of the small intestine in humans. Gut 47(5):632–637PubMedCentral CrossRef PubMed 6.Sonis ST (2004) A biological approach to mucositis. J Support Oncol 2(1):21–32 discussion 35-6PubMed 7.Sonis ST (2004) Pathobiology of mucositis. Semin Oncol Nurs 20(1):11–15CrossRef PubMed 8.Al-Dasooqi N et al. (2013) Emerging evidence on the pathobiology of mucositis. Support Care Cancer 21(7):2075–2083CrossRef PubMed 9.Gonzalez-Mariscal L, Tapia R, Chamorro D (2008) Crosstalk of tight junction components with signaling pathways. Biochim Biophys Acta 1778(3):729–756CrossRef PubMed 10.Wardill HR et al. (2014) Irinotecan disrupts tight junction proteins within the gut: implications for chemotherapy-induced gut toxicity. Cancer Biol Ther 15(2):236–244PubMedCentral CrossRef PubMed 11.Wardill HR, Bowen JM, Gibson RJ (2012) Chemotherapy-induced gut toxicity: are alterations to intestinal tight junctions pivotal? Cancer Chemother Pharmacol 70(5):627–635CrossRef PubMed 12.Keefe DM et al. (1997) Effect of high-dose chemotherapy on intestinal permeability in humans. Clin Sci 92(4):385–389CrossRef PubMed 13.Wardill HR et al. (2014) Irinotecan disrupts tight junction proteins within the gut: implications for chemotherapy-induced gut toxicity. Cancer Biol Ther 15(2):236–244PubMedCentral CrossRef PubMed 14.Hamada K et al. (2013) Disruption of ZO-1/claudin-4 interaction in relation to inflammatory responses in methotrexate-induced intestinal mucositis. Cancer Chemother Pharmacol 72(4):757–765CrossRef PubMed 15.Hamada K et al. (2010) Zonula Occludens-1 alterations and enhanced intestinal permeability in methotrexate-treated rats. Cancer Chemother Pharmacol 66(6):1031–1038CrossRef PubMed 16.Beutheu Youmba S et al. (2012) Methotrexate modulates tight junctions through NF-kappaB, MEK, and JNK pathways. J Pediatr Gastroenterol Nutr 54(4):463–470CrossRef PubMed 17.Nakao T et al. (2012) Irinotecan injures tight junction and causes bacterial translocation in rat. J Surg Res 173(2):341–347CrossRef PubMed 18.Edelblum KL, Turner JR (2009) The tight junction in inflammatory disease: communication breakdown. Curr Opin Pharmacol 9(6):715–720PubMedCentral CrossRef PubMed 19.Rebuffat SA et al. (2013) IL-1beta and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases. Immunobiology 218(3):285–291CrossRef PubMed 20.Schulzke JD et al. (2009) Epithelial tight junctions in intestinal inflammation. Ann N Y Acad Sci 1165:294–300CrossRef PubMed 21.Logan RM et al. (2008) Serum levels of NFkappaB and pro-inflammatory cytokines following administration of mucotoxic drugs. Cancer Biol Ther 7(7):1139–1145CrossRef PubMed 22.Al-Dasooqi N et al. (2011) Irinotecan-induced alterations in intestinal cell kinetics and extracellular matrix component expression in the dark agouti rat. Int J Exp Pathol 92(5):357–365PubMedCentral CrossRef PubMed 23.Cummins PM (2012) Occludin: one protein, many forms. Mol Cell Biol 32(2):242–250PubMedCentral CrossRef PubMed 24.Wardill HR, Bowen JM (2013) Chemotherapy-induced mucosal barrier dysfunction: an updated review on the role of intestinal tight junctions. Curr Opin Support Palliat Care 7(2):155–161CrossRef PubMed 25.Gibson RJ et al. (2006) Apoptosis occurs early in the basal layer of the oral mucosa following cancer chemotherapy. Asia Pac J Clin Oncol 2(1):10CrossRef 26.Al-Azri AR et al. (2014) Involvement of matrix metalloproteinases (MMP-3 and MMP-9) in the pathogenesis of irinotecan-induced oral mucositis, J Oral Pathol Med 27.Nakao T et al. (2012) Irinotecan injures tight junction and causes bacterial translocation in rat. J Surg Res 173(2):341–347CrossRef PubMed 28.Nassour H, Dubreuil JD (2014) Escherichia coli STb enterotoxin dislodges claudin-1 from epithelial tight junctions. PLoS One 9(11):p. e113273CrossRef PubMed 29.Ngendahayo Muzika C, Dubreuil JD (2013) Escherichia coli heat-stable toxin b impairs intestinal epithelial barrier function by altering tight junction proteins. Infect Immun 81(8):p. 2819–p. 2827CrossRef 30.Kimura K, Teranishi S, Nishida T (2009) Interleukin-1beta-induced disruption of barrier function in cultured human corneal epithelial cells. Invest Ophthalmol Vis Sci 50(2):597–603CrossRef PubMed 31.Al-Dasooqi N et al. (2010) Matrix metalloproteinases are possible mediators for the development of alimentary tract mucositis in the dark agouti rat. Exp Biol Med (Maywood) 235(10):1244–1256CrossRef 32.Logan RM et al. (2007) Nuclear factor-kappaB (NF-kappaB) and cyclooxygenase-2 (COX-2) expression in the oral mucosa following cancer chemotherapy. Oral Oncol 43(4):395–401CrossRef PubMed 33.Bertiaux-Vandaele N et al. (2011) The expression and the cellular distribution of the tight junction proteins are altered in irritable bowel syndrome patients with differences according to the disease subtype. Am J Gastroenterol 106(12):2165–2173CrossRef PubMed 34.Ma, T.Y., et al., Mechanism of TNF-{alpha} modulation of Caco-2 intestinal epithelial tight junction barrier: role of myosin light-chain kinase protein expression. Am J Physiol Gastrointes Liver Physiol, 2005. 288(3): p. G422-G430. 35.Ma TY et al. (2004) TNF-alpha-induced increase in intestinal epithelial tight junction permeability requires NF-kappa B activation. Am J Physiol Gastrointes Liver Physiol 286(3):G367–G376CrossRef 36.Al-Sadi R et al. (2008) Mechanism of IL-1beta-induced increase in intestinal epithelial tight junction permeability. J Immunol 180(8):5653–5661PubMedCentral CrossRef PubMed 37.Al-Dasooqi N, Wardill HR, Gibson RJ (2014) Gastrointestinal mucositis: the role of MMP-tight junction interactions in tissue injury. Pathol Oncol Res 20(3):485–491CrossRef PubMed 38.Vermeer PD et al. (2009) MMP9 modulates tight junction integrity and cell viability in human airway epithelia. Am J Physiol Lung Cell Mol Physiol 296(5):L751–L762PubMedCentral CrossRef PubMed 39.Jeong S et al. (2012) Interaction of clusterin and matrix metalloproteinase-9 and its implication for epithelial homeostasis and inflammation. Am J Physiol Gastrointes Liver Physiol 180(5):2028–2039
作者单位:Hannah R. Wardill (1) Richard M. Logan (2) Joanne M. Bowen (3) Ysabella Z. A. Van Sebille (3) Rachel J. Gibson (1)
1. Discipline of Anatomy and Pathology, School of Medicine, University of Adelaide, North Terrace, Adelaide, South Australia, 5005, Australia 2. School of Dentistry, University of Adelaide, Adelaide, South Australia, Australia 3. Discipline of Physiology, School of Medicine, University of Adelaide, Adelaide, South Australia, Australia
刊物类别:Medicine
刊物主题:Medicine & Public Health Oncology Nursing Nursing Management and Research Pain Medicine Rehabilitation Medicine
出版者:Springer Berlin / Heidelberg
ISSN:1433-7339
文摘
Purpose Oral mucositis is one of the most common and debilitating side effects of chemotherapy treatment. Patients are often unable to eat and drink, which can lead to poor clinical outcomes and extensive resource utilisation. The primary aim of this study was to determine the molecular integrity of oral epithelial tight junctions in patients undergoing chemotherapy. The secondary aim was to correlate these changes with proinflammatory cytokines and matrix metalloproteinase profiles.