NCOA1 Directly Targets M-CSF1 Expression to Promote Breast Cancer Metastasis

Cancer Res. 2014 Jul 1;74(13):3477-88. doi: 10.1158/0008-5472.CAN-13-2639. Epub 2014 Apr 25.

Abstract

In breast cancer, overexpression of the nuclear coactivator NCOA1 (SRC-1) is associated with disease recurrence and resistance to endocrine therapy. To examine the impact of NCOA1 overexpression on morphogenesis and carcinogenesis in the mammary gland (MG), we generated MMTV-hNCOA1 transgenic [Tg(NCOA1)] mice. In the context of two distinct transgenic models of breast cancer, NCOA1 overexpression did not affect the morphology or tumor-forming capability of MG epithelial cells. However, NCOA1 overexpression increased the number of circulating breast cancer cells and the efficiency of lung metastasis. Mechanistic investigations showed that NCOA1 and c-Fos were recruited to a functional AP-1 site in the macrophage attractant CSF1 promoter, directly upregulating colony-simulating factor 1 (CSF1) expression to enhance macrophage recruitment and metastasis. Conversely, silencing NCOA1 reduced CSF1 expression and decreased macrophage recruitment and breast cancer cell metastasis. In a cohort of 453 human breast tumors, NCOA1 and CSF1 levels correlated positively with disease recurrence, higher tumor grade, and poor prognosis. Together, our results define an NCOA1/AP-1/CSF1 regulatory axis that promotes breast cancer metastasis, offering a novel therapeutic target for impeding this process.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology*
  • Cell Line, Tumor
  • Female
  • Humans
  • Lung Neoplasms / genetics
  • Lung Neoplasms / secondary
  • Lymphatic Metastasis
  • MCF-7 Cells
  • Macrophage Activation / genetics
  • Macrophage Activation / immunology
  • Macrophage Colony-Stimulating Factor / biosynthesis
  • Macrophage Colony-Stimulating Factor / genetics*
  • Macrophages / immunology
  • Mammary Tumor Virus, Mouse
  • Mice
  • Mice, Transgenic
  • Neoplasm Recurrence, Local / genetics
  • Neoplastic Cells, Circulating / pathology
  • Nuclear Receptor Coactivator 1 / biosynthesis
  • Nuclear Receptor Coactivator 1 / genetics*
  • Proto-Oncogene Proteins c-fos / genetics
  • RNA Interference
  • RNA, Small Interfering
  • Transcription Factor AP-1 / genetics

Substances

  • Proto-Oncogene Proteins c-fos
  • RNA, Small Interfering
  • Transcription Factor AP-1
  • Macrophage Colony-Stimulating Factor
  • Nuclear Receptor Coactivator 1