Animal models of chemotherapy-induced mucositis: translational relevance and challenges

被引:53
|
作者
Sangild, Per T. [1 ,2 ,3 ]
Shen, Rene Liang [1 ]
Pontoppidan, Peter [1 ,2 ]
Rathe, Mathias [3 ]
机构
[1] Univ Copenhagen, Comparat Pediat & Nutr, Frederiksberg, Denmark
[2] Rigshosp, Dept Pediat & Adolescent Med, Copenhagen, Denmark
[3] Odense Univ Hosp, Hans Christian Andersen Childrens Hosp, Odense, Denmark
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2018年 / 314卷 / 02期
关键词
chemotherapy; inflammation; intestine; mice; mucositis; pig; rat; toxicity; STEM-CELL TRANSPLANTATION; INDUCED INTESTINAL MUCOSITIS; ACUTE LYMPHOBLASTIC-LEUKEMIA; MANNOSE-BINDING LECTIN; INDUCED GASTROINTESTINAL MUCOSITIS; ACUTE MYELOID-LEUKEMIA; DOXORUBICIN-INDUCED MUCOSITIS; ALIMENTARY-TRACT MUCOSITIS; PRO-INFLAMMATORY CYTOKINES; HIGH-DOSE CHEMOTHERAPY;
D O I
10.1152/ajpgi.00204.2017
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Chemotherapy for cancer patients induces damaging tissue reactions along the epithelium of the gastrointestinal tract (GIT). This chemotherapy-induced mucositis (CIM) is a serious side effect of cytotoxic drugs, and several animal models of CIM have been developed, mainly in rodents and piglets, to help understand the progression of CIM and how to prevent it. Animal models allow highly controlled experimental conditions, detailed organ (e.g., GIT) insights, standardized, clinically relevant treatment regimens, and discovery of new biomarkers. Still, surprisingly few results from animal models have been translated into clinical CIM management and treatments. The results obtained from specific animal models can be difficult to translate to the diverse range of CIM manifestations in patients, which vary according to the antineoplastic drugs, dose, underlying (cancer) disease, and patient characteristics (e.g., age, genetics, and body constitution). Another factor that hinders the direct use of results from animals is inadequate collaboration between basic science and clinical science in relation to CIM. Here, we briefly describe CIM pathophysiology, particularly the basic knowledge that has been obtained from CIM animal models. These model studies have indicated potential new preventive and ameliorating interventions, including supplementation with natural bioactive diets (e.g., milk fractions, colostrum, and plant extracts), nutrients (e.g., polyunsaturated fatty acids, short- chain fatty acids, and glutamine), and growth factor peptides (e.g., transforming growth factor and glucagon-like peptide-2), as well as manipulations of the gut microbiota (e.g., prebiotics, probiotics, and antibiotics). Rodent CIM models allow well-controlled, in-depth studies of animals with or without tumors while pig models more easily make clinically relevant treatment regimens possible. In synergy, animal models of CIM provide the basic physiological understanding and the new ideas for treatment that are required to make competent decisions in clinical practice.
引用
收藏
页码:G231 / G246
页数:16
相关论文
共 50 条
  • [31] Chemotherapy-induced metastasis: mechanisms and translational opportunities
    Karagiannis, G.
    Sanchez, L. Rivera
    Wang, Y.
    Sharma, V.
    Burt, J.
    Entenberg, D.
    Oktay, M.
    Condeelis, J.
    EUROPEAN JOURNAL OF CANCER, 2018, 103 : E51 - E51
  • [32] Animals Models of Gastrointestinal and Liver Diseases. Animal models of alcohol-induced liver disease: pathophysiology, translational relevance, and challenges
    Mathews, Stephanie
    Xu, Mingjiang
    Wang, Hua
    Bertola, Adeline
    Gao, Bin
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2014, 306 (10): : G819 - G823
  • [34] Efficacy of Rebamipide Gargle against Chemotherapy-induced Oral Mucositis
    Shinohara, Akiyoshi
    Nakamura, Masato
    Onikubo, Toshihide
    Nakamura, Kumi
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2015, 135 (08): : 937 - 941
  • [35] Expression of prostaglandin H synthase isoenzymes in chemotherapy-induced mucositis
    Shigematsu, H
    Leung, CK
    Wang, SL
    Feng, J
    WuWang, CY
    JOURNAL OF DENTAL RESEARCH, 1997, 76 : 1023 - 1023
  • [36] Chemotherapy-induced oral mucositis in children and adolescents: a systematic review
    Docimo, R.
    Anastasio, M. D.
    Bensi, C.
    EUROPEAN ARCHIVES OF PAEDIATRIC DENTISTRY, 2022, 23 (04) : 501 - 511
  • [37] Changes in the Mucus Barrier Are the "Causes" or "Results" of Chemotherapy-Induced Mucositis?
    Ichikawa, Takafumi
    Yamamoto, Hajime
    Kawakami, Fumitaka
    Kawashima, Rei
    Maekawa, Tatsunori
    Koizumi, Wasaburo
    GASTROENTEROLOGY, 2014, 146 (05) : S793 - S793
  • [38] Oral microbiota: An overlooked etiology for chemotherapy-induced oral mucositis?
    Wang, Yan
    Zhou, Xuedong
    Xu, Xin
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2015, 114 (04) : 297 - 299
  • [39] Protective effect of ursodeoxycholic acid against chemotherapy-induced mucositis
    Kim, Seung Han
    Chun, Hoon Jai
    Lee, Jae Min
    Choi, Hyuk Soon
    Kim, Eun Sun
    Keum, Bora
    Jeen, Yoon Tae
    Lee, Hong Sik
    Kim, Chang Duck
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2016, 31 : 131 - 131
  • [40] Matrix metalloproteinases: key regulators in the pathogenesis of chemotherapy-induced mucositis?
    Noor Al-Dasooqi
    Rachel J. Gibson
    Joanne M. Bowen
    Dorothy M. Keefe
    Cancer Chemotherapy and Pharmacology, 2009, 64 : 1 - 9