Changes in glucose-6-phosphate dehydrogenase expression results in altered behavior of HBV-associated liver cancer cells

Author:

Hu Huaidong123,Ding Xiangchun14,Yang Yixuan1,Zhang Hongmin1,Li Hong1,Tong Shiwen1,An Xuan1,Zhong Qing1,Liu Xiaoyan4,Ma Lina4,Liu Qing5,Liu Bin5,Lu Zhenhui5,Zhang Dazhi123,Hu Peng123,Ren Hong123

Affiliation:

1. Department of Infectious Diseases, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China;

2. Institute for Viral Hepatitis of Chongqing Medical University, Chongqing, China;

3. Key Laboratory of Molecular Biology for Infectious Diseases, Ministry of Education, Chongqing Medical University, Chongqing, China;

4. Department of Infectious Diseases, General Hospital of Ningxia Medical University, Yinchuan, Ning Xia, China; and

5. Department of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, Yinchuan, Ning Xia, China

Abstract

Hepatocellular carcinoma (HCC) is regarded as a major global health care issue, and chronic hepatitis B virus (HBV) infection is considered to be involved in pathogenesis of HCC. To increase knowledge of HCC pathogenesis, as well as discover potential novel molecules for anti-cancer therapy, mass spectrometry and isobaric tag for relative and absolute quantitation (iTARQ) were employed. The differences between nine HBV-related HCC and adjacent non-HCC tissue specimens were studied. In total, 222 proteins were analyzed for differential expression in the two types of samples. Among these proteins, several were further confirmed by immunohistochemical, immunoblotting, and real-time RT-PCR analysis. RNA interference induced downregulation of glucose-6-phosphate dehydrogenase (G6PD) and decreased HBV replication by fivefold by the IFN pathway. Decreased G6PD expression resulted in decreased hepatoma cell migration and invasion in cell culture. In summary, the investigation provides new information on pathogenesis of HBV infection and suggests G6PD as a novel anti-HCC target. G6PD suppression may contribute to treatment strategies for inhibiting tumor progression.

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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