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Showing papers by "Jun He published in 2012"


Journal ArticleDOI
TL;DR: It is shown that reactive oxygen species (ROS) induce both ERBB2 and ERBB3 expression in vitro and in vivo, and that ERBB 2 and ER BB3 expression is regulated by ROS via miR‐199a and miR-125b downregulation and DNA hypermethylation.
Abstract: Overexpression of ERBB2 or ERBB3 is associated with cancer development and poor prognosis. In this study, we show that reactive oxygen species (ROS) induce both ERBB2 and ERBB3 expression in vitro and in vivo. We also identify that miR-199a and miR-125b target ERBB2 and/or ERBB3 in ovarian cancer cells, and demonstrate that ROS inhibit miR-199a and miR-125b expression through increasing the promoter methylation of the miR-199a and miR-125b genes by DNA methyltransferase 1. These findings reveal that ERBB2 and ERBB3 expression is regulated by ROS via miR-199a and miR-125b downregulation and DNA hypermethylation.

116 citations


Journal ArticleDOI
TL;DR: In this paper, the effect of apigenin via oral administration on tumor growth and metastasis remains unknown, however, the authors developed an orthotopic ovarian tumor model in nude mice and showed that apigenins inhibited the micrometastasis of cancer cells in the animal tumor model.
Abstract: Apigenin, a flavonoid commonly present in the daily diet, is known for its potential anti-tumor properties. However, the effect of apigenin via oral administration on tumor growth and metastasis remains unknown. In this study we developed an orthotopic ovarian tumor model in nude mice to test the effect of apigenin oral administration, and showed that apigenin inhibited the micrometastasis of cancer cells in the animal tumor model. To understand the mechanism of apigenin in inhibiting metastasis, we found that apigenin greatly inhibited MMP-9 expression and p-AKT and p-p70S6K1 levels in the tumor tissues compared to the control group. We further demonstrated that the downregulation of MMP-9 by apigenin was mediated by the AKT/p70S6K1 pathway. These findings help to address the question with common interests to the public of whether oral uptake of flavonoids is effective in preventing cancer. Our results demonstrate for the first time that oral uptake of apigenin can inhibit tumor metastasis through MMP-9 expression using the orthotopic ovarian tumor model.

39 citations