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Experimental Animal Models of Pancreatic Carcinogenesis for Prevention Studies and Their Relevance to Human Disease

机译:预防性胰腺癌发生的实验动物模型及其与人类疾病的关系

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摘要

Pancreatic cancer is difficult to cure, so its prevention is very important. For this purpose, animal model studies are necessary to develop effective methods. Injection of N-nitrosobis(2-oxopropyl)amine (BOP) into Syrian golden hamsters is known to induce pancreatic ductal adenocarcinomas, the histology of which is similar to human tumors. Moreover, K-ras activation by point mutations and p16 inactivation by aberrant methylation of 5′ CpG islands or by homozygous deletions have been frequently observed in common in both the hamster and humans. Thus, this chemical carcinogenesis model has an advantage of histopathological and genetic similarity to human pancreatic cancer, and it is useful to study promotive and suppressive factors. Syrian golden hamsters are in a hyperlipidemic state even under normal dietary conditions, and a ligand of peroxizome proliferator-activated receptor gamma was found to improve the hyperlipidemia and suppress pancreatic carcinogenesis. Chronic inflammation is a known important risk factor, and selective inhibitors of inducible nitric oxide synthase and cyclooxygenase-2 also have protective effects against pancreatic cancer development. Anti-inflammatory and anti-hyperlipidemic agents can thus be considered candidate chemopreventive agents deserving more attention.
机译:胰腺癌很难治愈,因此预防非常重要。为此,必须进行动物模型研究以开发有效的方法。已知将N-亚硝基双(2-氧丙基)胺(BOP)注入叙利亚金仓鼠会诱发胰腺导管腺癌,其组织学与人类肿瘤相似。此外,在仓鼠和人类中都经常观察到由点突变引起的K-ras激活和由5'CpG岛的异常甲基化或纯合缺失引起的p16失活。因此,该化学致癌模型具有与人胰腺癌的组织病理学和遗传相似性的优点,并且对研究促动和抑制因子是有用的。即使在正常饮食条件下,叙利亚金仓鼠也处于高脂血症状态,并且发现过氧化物酶体增殖物激活的受体γ的配体可改善高脂血症并抑制胰腺癌变。慢性炎症是已知的重要危险因素,诱导型一氧化氮合酶和环加氧酶-2的选择性抑制剂也对胰腺癌的发展具有保护作用。因此,抗炎药和抗高血脂药可被视为候选化学预防药,值得更多关注。

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