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DOI 10.1089/gtmb.2012.0242

Медицинская библиотека · Genetic testing and molecular biomarkers · 2012

BORIS, brother of the regulator of imprinted sites, is aberrantly expressed in hepatocellular carcinoma.

Chen Kefei, Huang Wenqing, Huang Bin, Wei YongGang, Li Bo, Ge Yan, Qin Yang

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

The brother of the regulator of imprinted sites (BORIS) is a novel member of the cancer testis antigen gene family, which are normally expressed only in spermatocytes, but abnormally activated in different malignancies.

AIM: The aim of this study was to explore the expression of BORIS in hepatocellular carcinoma (HCC) and its correlation with the clinicopathologic features and prognosis of HCC.

METHODS

We investigated BORIS expression in HCC cell lines and 105 primary HCC clinical surgical specimens using real-time polymerase chain reaction and Western blot analysis. We further examined the correlation of BORIS with a liver stem cell marker (CD90) in HCC tissues by histochemical double staining. The correlation of BORIS with clinicopathologic features and prognosis of HCC was analyzed using patient data.

RESULTS

The expression of BORIS was found in SMMC-7721, BEL-7402, and Huh-7, but not in hep-G2 cells. The expression rate of BORIS was significantly higher in the HCC tissues than in the adjacent noncancerous tissues (p=0.000). BORIS expression was correlated with the tumor size (p=0.000), CD90 expression (p=0.000), and satellite nodule (p=0.000). Kaplan-Meier survival curves showed that patients with positive expression of BORIS had lower overall survival rate (p=0.003).

CONCLUSIONS

Our data indicate that BORIS may be an auxiliary diagnosis index and a novel favorable prognostic indicator of HCC.

Для цитирования: Chen Kefei, Huang Wenqing, Huang Bin, Wei YongGang, Li Bo, Ge Yan, Qin Yang. BORIS, brother of the regulator of imprinted sites, is aberrantly expressed in hepatocellular carcinoma.. Genetic testing and molecular biomarkers. 2012. DOI: 10.1089/gtmb.2012.0242.

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