Abstract

The age dependence of the oval cell response and bile duct carcinomas of male F344 rats exposed to a cyclic choline deficiency-ethionine (CDE) diet (2 weeks on, 1 week off) supports the concept of loss of potential of liver stem cells to form cancers with aging. Livers of rats exposed at 3 weeks of age demonstrated a robust and widespread oval cell proliferation followed by cholangiofibrosis and bile duct metaplasia with extensive mucinous cysts throughout all lobes, and induction of cholangiocarcinomas (CCAs) in seven of eight rats. Livers of rats exposed beginning at 8 weeks of age had much less oval cell response and cholangiofibrosis with only 1 of 15 rats developing a CCA. Livers in old (10-12 months when started) rats remained virtually unaffected, with minimal oval cell proliferation, only occasional and small foci of ductular dysplasia, and none of 16 rats developed CCAs. In contrast to most published studies using uninterrupted choline deficiency plus a carcinogen, hepatocellular carcinoma (HCC) was not observed under the conditions of this study. With aging, male F344 rats exposed to cyclic CDE diet display a diminished oval cell response and fewer CCAs. The absence of HCC is possibly due to the fact that during cyclic CDE, the week off may allow putative liver stem cells to avoid death or differentiation and survive to give rise to CCAs, whereas with continuous CDE exposure, the stem cells are forced to differentiate and develop into HCCs with relatively few CCAs.

Highlights

  • The stem cell theory of cancer posits that cancers arise from tissue-determined stem cells present in various organs [1, 2]

  • The histologic grading of early changes for each experimental animal fed the choline deficiency-ethionine (CDE) diet is presented in Supplemental Table 1, and the results are summarized in Text Table 1 and Text Figures 2A and 2B

  • The oval cell response increased from CDE cycle 1 to 3 to 5 in the rats started at 3 weeks of age, but it decreased after 3 cycles in the rats started at 8 weeks and in the retired breeders

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Summary

Introduction

The stem cell theory of cancer posits that cancers arise from tissue-determined stem cells present in various organs [1, 2]. We compare cellular responses in the livers of rats exposed to hepatocarcinogenesis beginning at 3 weeks of age, beginni at 8 weeks of age, and in retired breeders (10 to 12 months), using a previously well studied chemical regimen, choline deficiency-ethionine (CDE) 8–10. Following the hierarchical model of Pierce et al 11, combined with analysis of the cellular events during chemical hepatocarcinogenesis, we previously concluded that, in adults, liver cancers can arise from liver stem cells (oval cells), transit-amplifying cells (ducts or immature hepatocytes), or mature hepatocytes, depending on the stage of maturation arrest [12,13,14,15]. HB completes the cellular lineage of liver cancer that extends from pluripotent stem cells to liver-determined stem cells to ductular stem cells to mature liver cells (Text Fig 1A)

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