Construction of a recombinant eukaryotic human ZHX1 gene expression plasmid and the role of ZHX1 in hepatocellular carcinoma

Wang,Jianping; Liu,Dejie; Liang,Xiaohong; Gao,Lifen; Yue,Xuetian; Yang,Yang; Ma,Chunhong; Liu,Jun

doi:10.3892/mmr.2013.1700

Construction of a recombinant eukaryotic human ZHX1 gene expression plasmid and the role of ZHX1 in hepatocellular carcinoma

Authors:
- Jianping Wang
- Dejie Liu
- Xiaohong Liang
- Lifen Gao
- Xuetian Yue
- Yang Yang
- Chunhong Ma
- Jun Liu
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Affiliations: Department of General Surgery, Provincial Hospital Affiliated to Shandong University, Jinan, Shandong 250012, P.R. China, Department of Anesthesiology, Qilu Hospital of Shandong University, Jinan, Shandong 250012, P.R. China, Key Laboratory for Experimental Teratology of Ministry of Education and Institute of Immunology, Shandong University School of Medicine, Jinan, Shandong 250012, P.R. China, Department of General Surgery, Dongying People's Hospital, Dongying, Shandong 257091, P.R. China
Published online on: September 24, 2013 https://doi.org/10.3892/mmr.2013.1700
Pages: 1531-1536

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Abstract

The zinc‑fingers and homeoboxes protein 1 (ZHX1) consists of 873 amino acid residues, is localized in the cell nucleus and appears to act as a transcriptional repressor. Previous studies have shown that ZHX1 interacts with nuclear factor Y subunit α (NF‑YA), DNA methyltransferases (DNMT) 3B and ZHX2, all of which are involved in tumorigenesis. However, the exact role of ZHX1 in tumorigenesis remains unknown. The aim of the current study was to construct a recombinant eukaryotic expression plasmid containing the human ZHX1 (hZHX1) gene and to investigate the biological activities of ZHX1 in hepatocellular carcinoma (HCC). Reverse transcription‑polymerase chain reaction (RT‑PCR) was used to amplify the N‑ and C‑terminal fragments (ZHX1‑N and ZHX1‑C, respectively) of the hZHX1 gene. The two PCR fragments were cloned into the pEASY‑T1 vector and subcloned into the pcDNA3 plasmid to generate a recombinant pcDNA3‑ZHX1 plasmid. Following identification by enzyme digestion and DNA sequencing, the recombinant pcDNA3‑ZHX1 plasmid was transfected into SMMC‑7721 cells. The level of ZHX1 expression was detected by RT‑PCR and western blot analysis. Cell growth curve assays were used to evaluate the effect of ZHX1 on cell proliferation. Moreover, the differential expression of ZHX1 between cancer and adjacent cirrhotic liver tissue was investigated by quantitative PCR (qPCR). Enzyme digestion and DNA sequencing confirmed the successful construction of the recombinant plasmid, pcDNA3‑ZHX1. qPCR and western blot analysis demonstrated that ZHX1 was efficiently expressed in SMMC‑7721 cells and overexpression of ZHX1 may inhibit the proliferation of SMMC‑7721 cells. In addition, reduced ZHX1 expression is widespread among cancer tissues from HCC patients. In conclusion, a recombinant eukaryotic expression plasmid, pcDNA3‑ZHX1, was successfully constructed. In addition, the current results indicate that a low expression of ZHX1 may be responsible for hepatocarcinogenesis.

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