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-kappaB 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.

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

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...

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Interfering Breast Cancer Metastases by Blocking NGAL Function PRINCIPAL INVESTIGATOR:

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عنوان ژورنال:
  • Cancer research

دوره 69 22  شماره 

صفحات  -

تاریخ انتشار 2009