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ID1 Promotes Breast Cancer Metastasis by S100A9 Regulation

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单位: [1]Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA [2]Fox Chase Canc Ctr, Canc Biol Program, Philadelphia, PA 19111 USA [3]Univ Washington, Med Ctr, Seattle, WA 98195 USA [4]Huazhong Univ Sci & Technol,Tongji Med Coll,Tongji Hosp,Dept Urol,Wuhan 430074,Peoples R China [5]Huazhong Univ Sci & Technol,Tongji Med Coll,Tongji Hosp,Inst Urol,Wuhan 430074,Peoples R China [6]Univ Penn, Ctr Res Early Detect & Cure Ovarian Canc, Philadelphia, PA 19104 USA [7]Univ Penn, Dept Obstet & Gynecol, Philadelphia, PA 19104 USA
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Metastasis is a major factor responsible for mortality in patients with breast cancer. Inhibitor of DNA binding 1 (Id1) has been shown to play an important role in cell differentiation, tumor angiogenesis, cell invasion, and metastasis. Despite the data establishing Id1 as a critical factor for lung metastasis in breast cancer, the pathways and molecular mechanisms of Id1 functions in metastasis remain to be defined. Here, we show that Id1 interacts with TFAP2A to suppress S100A9 expression. We show that expression of Id1 and S100A9 is inversely correlated in both breast cancer cell lines and clinical samples. We also show that the migratory and invasive phenotypes in vitro and metastasis in vivo induced by Id1 expression are rescued by reestablishment of S100A9 expression. S100A9 also suppresses the expression of known metastasis-promoting factor RhoC activated by Id1 expression. Our results suggest that Id1 promotes breast cancer metastasis by the suppression of S100A9 expression. (C) 2014 AACR.

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出版当年[2013]版:
大类 | 2 区 医学
小类 | 3 区 细胞生物学 3 区 肿瘤学
最新[2025]版:
大类 | 2 区 医学
小类 | 3 区 细胞生物学 3 区 肿瘤学
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出版当年[2012]版:
Q1 ONCOLOGY Q2 CELL BIOLOGY
最新[2023]版:
Q2 CELL BIOLOGY Q2 ONCOLOGY

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第一作者单位: [1]Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
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通讯机构: [1]Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA [*1]Wistar Inst Anat & Biol, 3601 Spruce St, Philadelphia, PA 19104 USA
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