Caveolin-1 mediates inflammatory breast cancer cell invasion via the Akt1 pathway and RhoC GTPase

J Cell Biochem. 2015 Jun;116(6):923-33. doi: 10.1002/jcb.25025.

Abstract

With a propensity to invade the dermal lymphatic vessels of the skin overlying the breast and readily metastasize, inflammatory breast cancer (IBC) is arguably the deadliest form of breast cancer. We previously reported that caveolin-1 is overexpressed in IBC and that RhoC GTPase is a metastatic switch responsible for the invasive phenotype. RhoC-driven invasion requires phosphorylation by Akt1. Using a reliable IBC cell line we set out to determine if caveolin-1 expression affects RhoC-mediated IBC invasion. Caveolin-1 was down regulated by introduction of siRNA or a caveolin scaffolding domain. The ability of the cells to invade was tested and the status of Akt1 and RhoC GTPase examined. IBC cell invasion is significantly decreased when caveolin-1 is down regulated. Activation of Akt1 is decreased when caveolin-1 is down regulated, leading to decreased phosphorylation of RhoC GTPase. Thus, we report here that caveolin-1 overexpression mediates IBC cell invasion through activation Akt1, which phosphorylates RhoC GTPase.

Keywords: CAVEOLIN-1; INFLAMMATORY BREAST CANCER; INVASION; METASTASIS; RhoC GTPase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism*
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Cell Proliferation / radiation effects
  • Cell Survival / genetics
  • Cell Survival / physiology
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Inflammatory Breast Neoplasms / genetics
  • Inflammatory Breast Neoplasms / metabolism*
  • Inflammatory Breast Neoplasms / pathology*
  • Mice
  • Neoplasm Invasiveness / genetics
  • Neoplasm Invasiveness / pathology
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • RNA, Small Interfering
  • rho GTP-Binding Proteins / genetics
  • rho GTP-Binding Proteins / metabolism*

Substances

  • Caveolin 1
  • RNA, Small Interfering
  • Proto-Oncogene Proteins c-akt
  • rho GTP-Binding Proteins