Cell, Tumor, and Stem Cell Biology Inhibition of Lipocalin 2 Impairs Breast Tumorigenesis and Metastasis

نویسندگان

  • Xiaohong Leng
  • Tian Ding
  • Hui Lin
  • Yan Wang
  • Limei Hu
  • Jianhua Hu
  • Barry Feig
  • Wei Zhang
  • Lajos Pusztai
  • W. Fraser Symmans
  • Yun Wu
  • Ralph B. Arlinghaus
چکیده

Lipocalin 2 (LCN2; also known as NGAL) is a secreted glycoprotein and its elevated expression has been observed in breast cancers. However, the importance of LCN2 in breast tumorigenesis is unclear. Here, we employed a spontaneous mammary tumor mouse model showing that MMTV-ErbB2 (V664E) mice lacking mouse LCN2 had significantly delayed mammary tumor formation and metastasis with reduced matrix metalloproteinase-9 activity in the blood. LCN2 expression is upregulated by HER2/phosphoinositide 3-kinase/ AKT/NF-κB pathway. Decreasing LCN2 expression significantly reduced the invasion and migration ability of HER2 breast cancer cells. Furthermore, injecting an anti-mouse LCN2 antibody into mice bearing established murine breast tumors resulted in significant blockage of lung metastasis. Our findings indicate that LCN2 is a critical factor in enhancing breast tumor formation and progression possibly in part by stabilizing matrix metalloproteinase-9. Our results suggest that inhibition of LCN2 function by an inhibitory monoclonal antibody has potential for breast cancer therapy, particularly by interfering with metastasis in aggressive types of breast cancer. [Cancer Res 2009;69(22):8579–84]

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تاریخ انتشار 2009