Heme oxygenase-1 (HO-1) plays an important role in the progression of several malignancies including breast cancer. However, its role in breast cancer metastasis is still ambiguous. In this study, we observed the effect of HO-1 on mouse mammary carcinoma metastasis using the in vivo
tumor metastasis model. Our results revealed that overexpression of HO-1 strongly inhibits the lung metastasis of 4T1 cells. In in vitro analysis, associated indices for epithelial‐mesenchymal transition (EMT), migration, and proliferation of 4T1 cells were evaluated. The results show
that HO-1 inhibits EMT, migration, and proliferation of 4T1 cells. In addition, the Notch1/Slug pathway is found to mediate an antimetastasis role of HO-1 in mouse mammary carcinoma. In conclusion, since HO-1/Notch1/Slug axis plays an important role in breast cancer metastasis, induction of
HO-1 could be used as a potential therapeutic strategy for breast cancer treatment.
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Epithelial‐mesenchymal transition (EMT);
Heme oxygenase-1 (HO-1);
Murine mammary carcinoma;
Document Type: Research Article
Department of Biochemistry and Molecular Biology, Harbin Medical University, Harbin, P.R. China
Publication date: June 21, 2019
This article was made available online on February 14, 2019 as a Fast Track article with title: "Heme Oxygenase-1 Inhibits Tumor Metastasis Mediated By Notch1 Pathway In Murine Mammary Carcinoma".
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