2017•Zhonghua shiyan waike zazhiRequires access

Effects of small interfering RNA transfection of B cell lymphoma/leukemia-2-associated athanogene-1 gene on biological characteristics of hepatocellular carcinoma cells

Zhiqiang Gao, Junfeng Wang, Dehua Chen, Xuesong Ma

Open publisher page 1 citations

Abstract

Objective To investigate the effect of B cell lymphoma/leukemia-2-associated athanogene-1 gene (BAG-1) gene expression by RNA interference on the proliferation, apoptosis and Wnt/β-catenin signaling pathway in hepatocellular carcinoma cells. Methods Human normal liver cells L02 as control cells, reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting were used to detect the expression of BAG-1 in human hepatocellular carcinoma cell lines HepG2, Huh7, MHCC97L, MHCC97H and HCCLM3; the negative small interfering RNA (siRNA) and BAG-1-siRNA transfected HCCLM3 cells, and not transfected cells for the blank control group, transfection effect was detected after cells transfected for 48 h; the proliferation of the cells was detected by cell counting kit-8 (CCK-8) after cells were transfected at 24, 48 and 72 h; the cells apoptosis after cells were transfected for 48 h was detected by flow cytometry; β-catenin, Survivin, c-Myc protein expression were detected by Western blotting. Results The expression of BAG-1 in hepatocellular carcinoma cells were significantly higher than those of control cells L02 ((mRNA: PHepG2=0.000, PHuh7=0.000, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000; protein: PHepG2=0.030, PHuh7=0.001, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000); the expression of BAG-1 protein (0.097±0.010) after BAG-1-siRNA were transfected into HCCLM3 cells was significantly lower than the control Group (0.489±0.039) (P=0.000); the cells proliferation after BAG-1-siRNA transfected HCCLM3 cells for 48 h (0.312±0.024) and 72 h (0.673±0.051)were significantly lower than the control group (0.448±0.032), (0.673±0.051) (P48 h=0.004, P72 h=0.002); compared with the control group (2.13±0.11)%, (0.512±0.048), (0.349±0.032), (0.166±0.015), the apoptosis rate (13.47±1.05)% in BAG-1-siRNA group increased significantly, β-catenin (0.247±0.028), Survivin (0.153±0.017), c-Myc (0.089±0.009), protein expression was down regulated (Pβ-catenin=0.001, PSurvivin=0.001, Pc-Myc=0.002). Conclusion Inhibiting of BAG-1 expression can reduce the proliferation of hepatoma cells and promote apoptosis by inhibiting the Wnt/β-catenin signaling pathway. Key words: B cell lymphoma/leukemia-2-associated athanogene-1 gene; Liver cancer; Proliferation; Apoptosis; Wnt/β-catenin signaling pathway

About this research paper

What this paper is about

Objective To investigate the effect of B cell lymphoma/leukemia-2-associated athanogene-1 gene (BAG-1) gene expression by RNA interference on the proliferation, apoptosis and Wnt/β-catenin signaling pathway in hepatocellular carcinoma cells. Methods Human normal liver cells L02 as control cells, reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting were used to detect the expression of BAG-1 in human hepatocellular carcinoma cell lines HepG2, Huh7, MHCC97L, MHCC97H and HCCLM3; the negative small interfering RNA (siRNA) and BAG-1-siRNA transfected HCCLM3 cells, and not transfected cells for the blank control group, transfection effect was detected after cells transfected for 48 h; the proliferation of the cells was detected by cell counting kit-8 (CCK-8) after cells were transfected at 24, 48 and 72 h; the cells apoptosis after cells were transfected for 48 h was detected by flow cytometry; β-catenin, Survivin, c-Myc protein expression were detected by Western blotting. Results The expression of BAG-1 in hepatocellular carcinoma cells were significantly higher than those of control cells L02 ((mRNA: PHepG2=0.000, PHuh7=0.000, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000; protein: PHepG2=0.030, PHuh7=0.001, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000); the expression of BAG-1 protein (0.097±0.010) after BAG-1-siRNA were transfected into HCCLM3 cells was significantly lower than the control Group (0.489±0.039) (P=0.000); the cells proliferation after BAG-1-siRNA transfected HCCLM3 cells for 48 h (0.312±0.024) and 72 h (0.673±0.051)were significantly lower than the control group (0.448±0.032), (0.673±0.051) (P48 h=0.004, P72 h=0.002); compared with the control group (2.13±0.11)%, (0.512±0.048), (0.349±0.032), (0.166±0.015), the apoptosis rate (13.47±1.05)% in BAG-1-siRNA group increased significantly, β-catenin (0.247±0.028), Survivin (0.153±0.017), c-Myc (0.089±0.009), protein expression was down regulated (Pβ-catenin=0.001, PSurvivin=0.001, Pc-Myc=0.002). Conclusion Inhibiting of BAG-1 expression can reduce the proliferation of hepatoma cells and promote apoptosis by inhibiting the Wnt/β-catenin signaling pathway. Key words: B cell lymphoma/leukemia-2-associated athanogene-1 gene; Liver cancer; Proliferation; Apoptosis; Wnt/β-catenin signaling pathway

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To investigate the effect of B cell lymphoma/leukemia-2-associated athanogene-1 gene (BAG-1) gene expression by RNA interference on the proliferation, apoptosis and Wnt/β-catenin signaling pathway in hepatocellular carcinoma cells. Methods Human normal liver cells L02 as control cells, reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting were used to detect the expression of BAG-1 in human hepatocellular carcinoma cell lines HepG2, Huh7, MHCC97L, MHCC97H and HCCLM3; the negative small interfering RNA (siRNA) and BAG-1-siRNA transfected HCCLM3 cells, and not transfected cells for the blank control group, transfection effect was detected after cells transfected for 48 h; the proliferation of the cells was detected by cell counting kit-8 (CCK-8) after cells were transfected at 24, 48 and 72 h; the cells apoptosis after cells were transfected for 48 h was detected by flow cytometry; β-catenin, Survivin, c-Myc protein expression were detected by Western blotting. Results The expression of BAG-1 in hepatocellular carcinoma cells were significantly higher than those of control cells L02 ((mRNA: PHepG2=0.000, PHuh7=0.000, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000; protein: PHepG2=0.030, PHuh7=0.001, PMHCC97L=0.000, PMHCC97H=0.000, PHCCLM3=0.000); the expression of BAG-1 protein (0.097±0.010) after BAG-1-siRNA were transfected into HCCLM3 cells was significantly lower than the control Group (0.489±0.039) (P=0.000); the cells proliferation after BAG-1-siRNA transfected HCCLM3 cells for 48 h (0.312±0.024) and 72 h (0.673±0.051)were significantly lower than the control group (0.448±0.032), (0.673±0.051) (P48 h=0.004, P72 h=0.002); compared with the control group (2.13±0.11)%, (0.512±0.048), (0.349±0.032), (0.166±0.015), the apoptosis rate (13.47±1.05)% in BAG-1-siRNA group increased significantly, β-catenin (0.247±0.028), Survivin (0.153±0.017), c-Myc (0.089±0.009), protein expression was down regulated (Pβ-catenin=0.001, PSurvivin=0.001, Pc-Myc=0.002). Conclusion Inhibiting of BAG-1 expression can reduce the proliferation of hepatoma cells and promote apoptosis by inhibiting the Wnt/β-catenin signaling pathway. Key words: B cell lymphoma/leukemia-2-associated athanogene-1 gene; Liver cancer; Proliferation; Apoptosis; Wnt/β-catenin signaling pathway

Key concepts: Transfection, Small interfering RNA, Molecular biology, Cell culture, Cell growth, Flow cytometry, Leukemia, Cancer research

Related papers

Back to paper searchBrowse research topicsOriginal source
Effects of small interfering RNA transfection of B cell lymphoma/leukemia-2-associated athanogene-1 gene on biological characteristics of hepatocellular carcinoma cells — Research Paper | ScholarLens