Open Access
ARTICLE
Overexpression of Uric Acid Transporter SLC2A9 Inhibits Proliferation of Hepatocellular Carcinoma Cells
Xiaoying Han*1, Jing Yang†1, Dong Li‡, Zewei Guo§
* Department of Gastroenterology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science,
Xiangyang, Hubei, P.R. China
† Department of Oncology, Xuzhou City Hospital of Traditional Chinese Medicine, Xuzhou, P.R. China
‡ Department of Oncology, Xuzhou Central Hospital, Xuzhou, Jiangsu, P.R. China
§ Department of Internal Medicine, Huangshan Traditional Chinese Medicine, Huangshan, Anhui, P.R. China
Oncology Research 2019, 27(5), 533-540. https://doi.org/10.3727/096504018X15199489058224
Abstract
Hepatocellular carcinoma (HCC) is the third leading cause of cancer-associated mortality worldwide. Although
the mechanisms of HCC progression are not well understood, recent studies demonstrated the potential contribution of uric acid transporter SLC2A9 to tumor suppression. However, the roles and underlying mechanisms are still unknown. We aimed to study the roles and mechanisms of SLC2A9 in HCC. The present study
showed that SLC2A9 expression was decreased in human HCC tissues and cell lines. In addition, overexpression of SLC2A9 inhibited HCC cell proliferation. SCL2A9 induced HCC cell apoptosis by inhibiting the
expression of caspase 3. Our study also revealed that upregulation of SLC2A9 reduced intracellular reactive
oxygen species (ROS) accumulation. Furthermore, SLC2A9 increased the mRNA and protein expression of
tumor suppressor p53 in HCC cells. Probenecid inhibits SLC2A9-mediated uric acid transport, which promotes cell proliferation, inhibits cell apoptosis, induces intracellular ROS, and decreases the expression of
p53 in HCC cells. Therefore, the present study demonstrated that SLC2A9 may be a novel tumor suppressor
gene and a potential therapeutic target in HCC.
Keywords
Cite This Article
Han, X., Yang, J., Li, D., Guo, Z. (2019). Overexpression of Uric Acid Transporter SLC2A9 Inhibits Proliferation of Hepatocellular Carcinoma Cells.
Oncology Research, 27(5), 533–540. https://doi.org/10.3727/096504018X15199489058224