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烟草制品成分4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮及其代谢物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁醇对F344大鼠肺癌转移至胰腺的影响

Metastasis to the F344 Rat Pancreas from Lung Cancer Induced by 4-(Methylnitrosamino)- 1-(3-pyridyl)-1-butanone and Enantiomers of Its Metabolite 4-(Methylnitrosamino)-1-(3-pyridyl)- 1-butanol, Constituents of Tobacco Products.

作者信息

Kovi Ramesh C, Johnson Charles S, Balbo Silvia, Hecht Stephen S, O'Sullivan M Gerard

机构信息

1 Department of Veterinary Population Medicine, University of Minnesota, St. Paul, Minnesota, USA.

2 Masonic Cancer Center, University of Minnesota, St. Paul, Minnesota, USA.

出版信息

Toxicol Pathol. 2018 Feb;46(2):184-192. doi: 10.1177/0192623317751573. Epub 2018 Feb 1.

Abstract

Lung cancer is the most common cause of cancer-related deaths in humans worldwide. There is strong evidence that the tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and its metabolite 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) play an important role in carcinogenesis caused by tobacco products. NNK and racemic NNAL are reported to induce lung and pancreatic tumors in rats. The carcinogenicity in Fischer 344 rats of NNK, NNAL, and its enantiomers ( R)-NNAL and ( S)-NNAL has been studied recently, and all test compounds induced significant numbers of lung tumors. We report here the detailed histopathological and immunohistochemical characterization of these tumors and their aggressive nature as shown by their metastasis locally and to the pancreas. The spectrum of treatment-related histopathological findings comprised pulmonary alveolar/bronchiolar (A/B) epithelial hyperplasia, A/B adenomas, and A/B carcinomas. A/B carcinomas frequently exhibited local invasion/metastasis within the mediastinum and thoracic cavity and distant metastasis to the pancreas that was confirmed by immunohistochemistry using the lung-specific markers prosurfactant protein-C and club (Clara) cell-10. Our observation regarding metastasis to the pancreas was an important, and unexpected, finding in this study both for the experimental animal model and potential human relevance.

摘要

肺癌是全球人类癌症相关死亡的最常见原因。有充分证据表明,烟草特有的亚硝胺4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁酮(NNK)及其代谢物4-(甲基亚硝胺基)-1-(3-吡啶基)-1-丁醇(NNAL)在烟草制品导致的致癌过程中起重要作用。据报道,NNK和外消旋NNAL可在大鼠中诱发肺癌和胰腺癌。最近研究了NNK、NNAL及其对映体(R)-NNAL和(S)-NNAL在Fischer 344大鼠中的致癌性,所有受试化合物均诱发了大量肺癌。我们在此报告这些肿瘤的详细组织病理学和免疫组化特征,以及它们通过局部转移和转移至胰腺所显示的侵袭性。与治疗相关的组织病理学发现谱包括肺泡/细支气管(A/B)上皮增生、A/B腺瘤和A/B癌。A/B癌经常表现出纵隔和胸腔内的局部侵袭/转移以及通过使用肺特异性标志物表面活性蛋白-C和棒状(克拉拉)细胞-10的免疫组化证实的远处转移至胰腺。我们关于转移至胰腺的观察结果对于本研究中的实验动物模型和潜在的人类相关性而言都是一项重要且意外的发现。

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