机构:[1] Fudan Univ, Shanghai Med Coll, Dept Oncol, Dept Breast Surg,Breast Canc Inst,Shanghai Canc C, Shanghai 200433, Peoples R China[2] Kanazawa Univ, Canc Res Inst, Div Mol Bioregulat, Kanazawa, Ishikawa 920, Japan[3] Chongqing Med Univ, Affiliated Hosp 2, Dept Gen Surg, Chongqing, Peoples R China
Metastasis represents the major remaining cause of mortality in human breast cancer. Interleukin-8 (IL-8), a proinflammatory chemokine, plays an important role during tumor angiogenesis and metastasis. In this study, we found that IL-8 and ERbeta (ER beta) showed positive association. Overexpression of ER beta or PEA 3 could upregulate IL-8 promoter activity, mRNA and secretion; silencing of ER beta or PEA 3 decreased IL-8 mRNA and secretion. ER beta and PEA 3 increased IL-8 expression through binding to the IL-8 promoter and increased cell invasion. HER2 could increase ER beta and PEA 3 expression and their binding to the IL-8 promoter. We conclude that ER beta and PEA 3 play important roles in tumor invasion by regulating IL-8 expression, and HER2 maybe the upstream of ER beta and PEA3-IL-8 pathway.
第一作者机构:[1] Fudan Univ, Shanghai Med Coll, Dept Oncol, Dept Breast Surg,Breast Canc Inst,Shanghai Canc C, Shanghai 200433, Peoples R China
通讯作者:
通讯机构:[1] Fudan Univ, Shanghai Med Coll, Dept Oncol, Dept Breast Surg,Breast Canc Inst,Shanghai Canc C, Shanghai 200433, Peoples R China[*1]Fudan Univ, Shanghai Med Coll, Dept Oncol, Dept Breast Surg,Breast Canc Inst,Shanghai Canc C, Shanghai 200433, Peoples R China
推荐引用方式(GB/T 7714):
Chen Ying,Chen Li,Li Ji-Yu,et al.ERβ and PEA3 co-activate IL-8 expression and promote the invasion of breast cancer cells[J].CANCER BIOLOGY & THERAPY.2011,11(5):497-511.doi:10.4161/cbt.11.5.14667.
APA:
Chen, Ying,Chen, Li,Li, Ji-Yu,Mukaida, Naofumi,Wang, Qiaoqiao...&Shao, Zhi-ming.(2011).ERβ and PEA3 co-activate IL-8 expression and promote the invasion of breast cancer cells.CANCER BIOLOGY & THERAPY,11,(5)
MLA:
Chen, Ying,et al."ERβ and PEA3 co-activate IL-8 expression and promote the invasion of breast cancer cells".CANCER BIOLOGY & THERAPY 11..5(2011):497-511