Thorgeirsson U P, Gomez D E, Lindsay C K, Sinha C C, Adamson R H
Division of Cancer Etiology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Liver. 1996 Apr;16(2):71-83. doi: 10.1111/j.1600-0676.1996.tb00708.x.
A food-derived mutagenic heterocyclic aromatic amine, 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), is a potent hepatocarcinogen in cynomolgus monkeys. In an ongoing carcinogenesis study, 34 out of 40 monkeys dosed with IQ have developed malignant liver tumors. The histology and cytokeratin expression was examined in a total of 94 tumors and non-neoplastic lesions obtained from 34 cases. The majority of the tumors were classified as hepatocellular carcinoma. In some cases, a striking difference in the histological features between individual tumor nodules was suggestive of a multicentric origin. Intrahepatic vascular invasion was seen in 14 (41.2%) and metastases in 6 (17.6%) of the hepatocellular carcinoma cases. There was no evidence of regenerative hyperplasia or fibrosis in the parenchyma of the tumor-bearing livers. Clear-cell foci composed of glycogen-rich hepatocytes were the only macroscopic lesions detected prior to gross tumor development. Other liver lesions included dysplastic hepatocyte foci and areas of proliferating bile ductular like (oval) cells, located around the periportal areas and along the portal tracts. Expression of bile duct type cytokeratin 7 was observed in a few of the oval cells and non-malignant hepatocytes, as well as in some of the hepatocellular carcinoma nodules. This aberrant cytokeratin expression raises questions concerning the histogenesis of the IQ-induced hepatocellular carcinoma.
一种源自食物的诱变杂环芳香胺,2-氨基-3-甲基咪唑并[4,5-f]喹啉(IQ),是食蟹猴中的一种强效肝癌致癌物。在一项正在进行的致癌作用研究中,40只接受IQ给药的猴子中有34只患上了恶性肝肿瘤。对从34例病例中获得的总共94个肿瘤和非肿瘤性病变进行了组织学和细胞角蛋白表达检测。大多数肿瘤被归类为肝细胞癌。在某些情况下,单个肿瘤结节之间组织学特征的显著差异提示多中心起源。在14例(41.2%)肝细胞癌病例中观察到肝内血管侵犯,6例(17.6%)出现转移。在携带肿瘤的肝脏实质中没有再生性增生或纤维化的证据。由富含糖原的肝细胞组成的透明细胞灶是在大体肿瘤形成之前检测到的唯一宏观病变。其他肝脏病变包括发育异常的肝细胞灶以及位于门静脉周围区域和沿门静脉分支的增生性胆管样(卵圆)细胞区域。在一些卵圆细胞和非恶性肝细胞以及一些肝细胞癌结节中观察到胆管型细胞角蛋白7的表达。这种异常的细胞角蛋白表达引发了关于IQ诱导的肝细胞癌组织发生的问题。