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Cytokeratin 7/19 表达在 N-二乙基亚硝胺诱导的小鼠肝细胞病变中的作用:对组织发生的意义。

Cytokeratin 7/19 expression in N-diethylnitrosamine-induced mouse hepatocellular lesions: implications for histogenesis.

机构信息

Veterinary Sciences Department, University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal; Veterinary Science Department, Veterinary and Animal Science Research Centre (CECAV), University of Trás-os-Montes and Alto Douro (UTAD), Vila Real, Portugal.

出版信息

Int J Exp Pathol. 2014 Jun;95(3):191-8. doi: 10.1111/iep.12082. Epub 2014 Apr 15.

Abstract

Hepatocellular carcinoma (HCC) is a common malignancy with poor clinical outcome, whose histogenesis is the subject of intense debate. Specifically, expression of cytokeratins (CKs) 7 and 19, associated with aggressive biological behaviour, is proposed to reflect a possible progenitor cell origin or tumour dedifferentiation towards a primitive phenotype. This work addresses that problem by studying CKs 7 and 19 expression in N-diethylnitrosamine (DEN)-induced mouse HCCs. ICR mice were divided into six DEN-exposed and six matched control groups. Samples were taken from each group at consecutive time points. Hyperplastic foci (13 lesions) occurred at 29-40 weeks (groups 8, 10 and 12) with diffuse dysplastic areas (19 lesions) and with one hepatocellular adenoma (HCA) (at 29 weeks). HCCs (4 lesions) were observed 40 weeks after the first DEN administration (group 12). CKs 7 and 19 showed identical expression patterns and located to large, mature hepatocytes, isolated or in small clusters. Hyperplastic foci and the single HCA were consistently negative for both markers, while dysplastic areas and HCCs were positive. These results support the hypothesis that CKs 7 and 19 expression in hepatocellular malignancies results from a dedifferentiation process rather than from a possible progenitor cell origin.

摘要

肝细胞癌 (HCC) 是一种常见的恶性肿瘤,临床预后较差,其发生机制仍存在争议。具体来说,与侵袭性行为相关的细胞角蛋白 (CKs) 7 和 19 的表达被认为反映了可能的祖细胞起源或肿瘤向原始表型的去分化。本研究通过研究 N-二乙基亚硝胺 (DEN) 诱导的小鼠 HCC 中 CKs 7 和 19 的表达来解决这个问题。ICR 小鼠分为 DEN 暴露组和对照组,每组各 6 只。在连续的时间点从每组中取样本。增生灶(13 个病灶)于 29-40 周(第 8、10 和 12 组)出现,弥漫性异型增生区(19 个病灶)和一个肝细胞腺瘤(HCA)(第 29 周)。首次 DEN 给药后 40 周观察到 HCC(第 12 组)。CKs 7 和 19 的表达模式相同,定位于大而成熟的肝细胞,呈单个或小簇状分布。增生灶和单个 HCA 均对这两种标志物均为阴性,而异型增生区和 HCC 为阳性。这些结果支持 CKs 7 和 19 在肝细胞恶性肿瘤中的表达来源于去分化过程而不是可能的祖细胞起源的假说。

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