Abstract

Hepatocellular carcinoma (HCC) is more prevalent in men than women, but the reason for this gender disparity is not well understood. To investigate whether zebrafish could be used to study the gender disparity of HCC, we compared the difference of liver tumorigenesis between female and male fish during early tumorigenesis and long-term tumor progression in our previously established inducible and reversible HCC model – the krasV12 transgenic zebrafish. We found that male fish developed HCC faster than females. The male tumors were more severe from the initiation stage, characteristic of higher proliferation, activation of WNT/β-catenin pathway and loss of cell adhesion. During long-term tumor progression, the male tumors developed into more advanced multi-nodular tumors, whereas the female tumors remain uniform and homogenous. Moreover, regression of male tumors required longer time. We further investigated the role of sex hormones in krasV12 transgenic fish. Estrogen treatment showed tumor suppressing effect during early tumorigenesis through inhibiting cell proliferation, whereas androgen accelerated tumor growth by promoting cell proliferation. Overall, our study presented the zebrafish as a useful animal model for study of gender disparity of HCC.

Highlights

  • Our group has previously established several inducible and reversible Hepatocellular carcinoma (HCC) models in zebrafish by transgenic expression of selected oncogenes[14,15,16,17,18]

  • To examine whether there is a gender difference during early liver tumorigenesis in the krasV12 induced zebrafish HCC model, male and female krasV12 zebrafish were treated with 20 mg/L doxycycline for 10 days

  • We demonstrated that the zebrafish liver tumor model could be a valuable tool for studying the gender disparity of HCC

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Summary

Introduction

Our group has previously established several inducible and reversible HCC models in zebrafish by transgenic expression of selected oncogenes[14,15,16,17,18]. Homogeneous HCC across the entire liver was developed within one month of oncogene induction. Withdrawal of the chemical inducer caused the suppression of oncogene expression and led to a rapid liver tumor regression. We aim to investigate whether the inducible transgenic zebrafish model could model the gender disparity of HCC. The difference of liver tumorigenesis between female and male fish was examined during early tumorigenesis and long-term tumor progression using the kras transgenic line.

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