Transactivation of human osteopontin promoter by human T-cell leukemia virus type 1-encoded Tax protein

被引:16
作者
Zhang, Jing [1 ]
Yamada, Osamu [1 ]
Matsushita, Yoshihisa [1 ]
Chagan-Yasutan, Haorile [2 ]
Hattori, Toshio [2 ]
机构
[1] FUSO Pharmaceut Ind Ltd, Ctr Res & Dev, Joto Ku, Osaka 5368523, Japan
[2] Tohoku Univ, Sch Med, Dept Infect & Resp Dis, Sendai, Miyagi 980, Japan
关键词
HTLV-1; Tax; Transactivation; Osteopontin; PI3K/AKT; AP-1; NF-KAPPA-B; MAMMARY EPITHELIAL-CELLS; HEPATITIS-C VIRUS; HTLV-1; TAX; BREAST-CANCER; TRANSCRIPTIONAL REGULATION; HTLV-1-TRANSFORMED CELLS; TRANSFORMED-CELLS; SIGNALING PATHWAY; TRANSGENIC MICE;
D O I
10.1016/j.leukres.2009.08.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteopontin (OPN) is a cytokine that contributes substantially to the growth and metastasis in a wide spectrum of malignancies. We report here that OPN gene is transactivated by Tax protein of human T-cell leukemia virus type 1 (HTLV-1). Northern blot showed enhanced OPN gene expression in cells stably expressing Tax. Co-expression of Tax increased the reporter gene expression directed by OPN promoter. Tax-induced OPN activation was abrogated by treatment with LY294002 (PI3K inhibitor) or co-transfection with AKT siRNA, suggesting PI3K/AKT pathway is involved in Tax-mediated transactivation. Reporter assay with deletion mutants showed that the 5'-partial sequence between -765 and -660 of the OPN promoter is the region responsive to Tax, and further, disrupting the AP-1 site within this region abolished the OPN induction by Tax, indicating that Tax activation of OPN promoter is likely mediated by AP-1 site. This study suggests that OPN is one of the downstream mediators of aberrantly activated PI3K/AKT signaling by Tax, which may partially contribute to HTLV-1-associated leukemogenesis. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:763 / 768
页数:6
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