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化疗诱导性黏膜炎的动物模型:转化相关性和挑战。

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

机构信息

Comparative Pediatrics and Nutrition, University of Copenhagen , Frederiksberg , Denmark.

Department of Pediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen , Denmark.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2018 Feb 1;314(2):G231-G246. doi: 10.1152/ajpgi.00204.2017. Epub 2017 Oct 26.

Abstract

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.

摘要

癌症患者的化疗会引起胃肠道(GI)上皮的破坏性组织反应。这种化疗诱导的粘膜炎(CIM)是细胞毒性药物的严重副作用,已经开发了几种 CIM 动物模型,主要在啮齿动物和仔猪中,以帮助了解 CIM 的进展以及如何预防它。动物模型允许高度控制的实验条件、详细的器官(例如,胃肠道)见解、标准化的、与临床相关的治疗方案以及新生物标志物的发现。尽管如此,动物模型的结果很少被转化为临床 CIM 管理和治疗。从特定动物模型获得的结果可能难以转化为患者中不同的 CIM 表现,这些表现因抗肿瘤药物、剂量、基础(癌症)疾病和患者特征(例如年龄、遗传和体质)而异。另一个阻碍将动物结果直接用于临床的因素是基础科学与 CIM 临床科学之间的合作不足。在这里,我们简要描述 CIM 的病理生理学,特别是从 CIM 动物模型中获得的基础知识。这些模型研究表明了潜在的新的预防和改善干预措施,包括补充天然生物活性饮食(例如乳部分、初乳和植物提取物)、营养素(例如多不饱和脂肪酸、短链脂肪酸和谷氨酰胺)以及生长因子肽(例如转化生长因子和胰高血糖素样肽-2),以及对肠道微生物群的操纵(例如,益生元、益生菌和抗生素)。啮齿动物 CIM 模型允许对有或没有肿瘤的动物进行高度控制、深入的研究,而猪模型更容易使临床相关的治疗方案成为可能。协同作用下,CIM 的动物模型提供了基本的生理理解和新的治疗思路,这是在临床实践中做出合理决策所必需的。

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