Scavenger receptor class B type I regulates cellular cholesterol metabolism and cell signaling associated with breast cancer development

Breast Cancer Res. 2013;15(5):R87. doi: 10.1186/bcr3483.

Abstract

Introduction: Previous studies have identified cholesterol as an important regulator of breast cancer development. High-density lipoprotein (HDL) and its cellular receptor, the scavenger receptor class B type I (SR-BI) have both been implicated in the regulation of cellular cholesterol homeostasis, but their functions in cancer remain to be established.

Methods: In the present study, we have examined the role of HDL and SR-BI in the regulation of cellular signaling pathways in breast cancer cell lines and in the development of tumor in a mouse xenograft model.

Results: Our data show that HDL is capable of stimulating migration and can activate signal transduction pathways in the two human breast cancer cell lines, MDA-MB-231 and MCF7. Furthermore, we also show that knockdown of the HDL receptor, SR-BI, attenuates HDL-induced activation of the phosphatidylinositol 3-kinase (PI3K)/protein Kinase B (Akt) pathway in both cell lines. Additional investigations show that inhibition of the PI3K pathway, but not that of the mitogen-activated protein kinase (MAPK) pathway, could lead to a reduction in cellular proliferation in the absence of SR-BI. Importantly, whereas the knockdown of SR-BI led to decreased proliferation and migration in vitro, it also led to a significant reduction in tumor growth in vivo. Most important, we also show that pharmacological inhibition of SR-BI can attenuate signaling and lead to decreased cellular proliferation in vitro. Taken together, our data indicate that both cholesteryl ester entry via HDL-SR-BI and Akt signaling play an essential role in the regulation of cellular proliferation and migration, and, eventually, tumor growth.

Conclusions: These results identify SR-BI as a potential target for the treatment of breast cancer.

Publication types

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

MeSH terms

  • Animals
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • CD36 Antigens / genetics
  • CD36 Antigens / metabolism*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation
  • Cell Transformation, Neoplastic*
  • Cholesterol / metabolism*
  • Cholesterol / pharmacology
  • Cholesterol, HDL / metabolism
  • Cholesterol, HDL / pharmacology
  • Disease Models, Animal
  • Enzyme Activation / drug effects
  • Female
  • Gene Knockdown Techniques
  • Heterografts
  • Humans
  • Lipoproteins, HDL / genetics
  • Lipoproteins, HDL / metabolism
  • MCF-7 Cells
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptors, Lipoprotein / genetics
  • Receptors, Lipoprotein / metabolism
  • Signal Transduction*
  • Tumor Burden / genetics

Substances

  • CD36 Antigens
  • Cholesterol, HDL
  • Lipoproteins, HDL
  • Receptors, Lipoprotein
  • high density lipoprotein receptors
  • Cholesterol
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3