Expressions of BIRC6 in hepatocellular carcinoma and their effects on apoptosis of hepatocellular carcinoma cell
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Expressions of BIRC6 in hepatocellular carcinoma and their effects on apoptosis of hepatocellular carcinoma cell
Journal of Chongqing Medical UniversityVol. 36, Issue 9, Pages: 1022-1026(2013)
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浙江省杭州市下沙医院普外科,杭州,310018
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Published:2013,
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JIANG Jinwei, YANG Xiaoyan. Expressions of BIRC6 in hepatocellular carcinoma and their effects on apoptosis of hepatocellular carcinoma cell. [J]. Journal of Chongqing Medical University 36(9):1022-1026(2013)
DOI:
JIANG Jinwei, YANG Xiaoyan. Expressions of BIRC6 in hepatocellular carcinoma and their effects on apoptosis of hepatocellular carcinoma cell. [J]. Journal of Chongqing Medical University 36(9):1022-1026(2013)DOI:
Expressions of BIRC6 in hepatocellular carcinoma and their effects on apoptosis of hepatocellular carcinoma cell
Objective:To investigate the expressions of baculoviral IAP repeat-containing 6(BIRC6) and their role in hepatocellular carcinoma(HCC). Methods:Forty samples of surgically resected HCC tissues and corresponding adjacent tissues were collected and BIRC6 expressions in HCC tissues and corresponding adjacent tissues were detected using qRT-PCR and immunohistochemistry. BIRC6 mRNA expressions in normal liver cell line(LO2) and HCC cell lines(HepG2 and SMMC-7721) were detected using qRT-PCR. BIRC6 siRNA was transfected into SMMC-7721 cells and cell viability and apoptosis were analyzed by MTT and flow cytometry. Results:Expressions of BIRC6 in HCC tissues were significantly upregulated compared with those in corresponding adjacent tissues(P=0.004). Clinicopathological evaluation suggested that BIRC6 high-expression was associated with large tumor size(> 5 cm) and advanced TNM stage(P=0.029;P=0.002). Expressions of BIRC6 mRNA were obviously lower in LO2 than in HepG2 and SMMC-7721(P=0.000). siRNA suppressed expression of BIRC6 in SMMC-7721 cells decreased cell viability and increased cell apoptosis(P=0.000). Conclusions:High-expression of BIRC6 correlates with poor clinicopathological characteristics in HCC and BIRC6 may act as an inhibitor of apoptosis as well as a therapeutic target of HCC.