Abstract

Aim. To investigate the relationship between alpha-fetoprotein and zinc fingers and homeoboxes 2 in hepatocellular carcinoma. Materials and Methods. The expressions of zinc fingers and homeoboxes 2, nuclear factor-YA, and alpha-fetoprotein mRNA in 63 hepatocellular carcinoma were detected by reverse transcriptase-polymerase chain reaction and compared with the clinical parameters of the patients. Selectively, silence of zinc fingers and homeoboxes 2 in HepG2 cells was detected by RNA interference technique. Results. Alpha-fetoprotein mRNA expression was detected in 60.3% of hepatocellular carcinoma cases. Zinc fingers and homeoboxes 2 mRNA expression (36.5%) was significantly negatively correlated with serum alpha-fetoprotein concentration and mRNA expression. A strong positive correlation was found between zinc fingers and homeoboxes 2 and nuclear factor-YA mRNA expression (42.9%), while the latter was negatively correlated with serum alpha-fetoprotein concentration and mRNA expression. Treatment with zinc fingers and homeoboxes 2 small interfering RNA led to 85% and 83% silence of zinc fingers and homeoboxes 2 mRNA and protein expression and 60% and 61% reduction of nuclear factor-YA mRNA and protein levels in the HepG2 cells, respectively. Downregulation of zinc fingers and homeoboxes 2 also induced a 2.4-fold increase in both alpha-fetoprotein mRNA and protein levels. Conclusions. Zinc fingers and homeoboxes 2 can regulate alpha-fetoprotein expression via the interaction with nuclear factor-YA in human hepatocellular carcinoma and may be used as an adjuvant diagnostic marker for alpha-fetoprotein-negative hepatocellular carcinoma.

Highlights

  • Alpha-fetoprotein (AFP) is one of the major serum proteins in fetal mammals

  • zinc fingers and homeoboxes 2 (ZHX2) is a novel transcriptional repressor, which consists of 837 amino acid residues

  • We previously found that promoter hypermethylation caused a low mRNA expression of ZHX2 in hepatocellular carcinoma (HCC)

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Summary

Introduction

Alpha-fetoprotein (AFP) is one of the major serum proteins in fetal mammals. Olsson et al found that the average AFP level in the BALB/cJ mice is about 10-fold higher than that of the controls (C3H/He and BALB/c/BOM) 9-10 weeks postnatally [2]. The postnatal AFP level in BALB/cJ mice is controlled by a single recessive Mendelian gene, previously named raf (regulation of alphafetoprotein) and renamed Afr (alpha-fetoprotein regulator 1) [3]. Afr governs postnatal AFP mRNA levels in adult mice liver [4, 5]. In adult BALB/cJ mice, retrotransposon insertion in ZHX2 reduces its mRNA expression, resulting in an elevated expression of AFP [7]. With cirrhosis 11 (34.4) Grade I-II 15 (34.9) 1.24 (.42–3.71) III-IV 8 (40) Metastasis Without

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