Activation of the MKL1/actin signaling pathway induces hormonal escape in estrogen-responsive breast cancer cell lines

Mol Cell Endocrinol. 2014 Jun 5;390(1-2):34-44. doi: 10.1016/j.mce.2014.03.009. Epub 2014 Apr 8.

Abstract

Estrogen receptor alpha (ERα) is generally considered to be a good prognostic marker because almost 70% of ERα-positive tumors respond to anti-hormone therapies. Unfortunately, during cancer progression, mammary tumors can escape from estrogen control, resulting in resistance to treatment. In this study, we demonstrate that activation of the actin/megakaryoblastic leukemia 1 (MKL1) signaling pathway promotes the hormonal escape of estrogen-sensitive breast cancer cell lines. The actin/MKL1 signaling pathway is silenced in differentiated ERα-positive breast cancer MCF-7 and T47D cell lines and active in ERα-negative HMT-3522 T4-2 and MDA-MB-231 breast cancer cells, which have undergone epithelial-mesenchymal transition. We showed that MKL1 activation in MCF-7 cells, either by modulating actin dynamics or using MKL1 mutants, down-regulates ERα expression and abolishes E2-dependent cell growth. Interestingly, the constitutively active form of MKL1 represses PR and HER2 expression in these cells and increases the expression of HB-EGF, TGFβ, and amphiregulin growth factors in an E2-independent manner. The resulting expression profile (ER-, PR-, HER2-) typically corresponds to the triple-negative breast cancer expression profile.

Keywords: Breast cancer; Cell growth; Estrogen receptor; Hormone resistance; MKL1; Tamoxifen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Antineoplastic Agents, Hormonal / pharmacology
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / metabolism*
  • DNA-Binding Proteins / metabolism*
  • Drug Resistance, Neoplasm
  • Estradiol / physiology
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / metabolism
  • Female
  • Humans
  • MCF-7 Cells
  • Neoplasms, Hormone-Dependent / drug therapy
  • Neoplasms, Hormone-Dependent / metabolism
  • Oncogene Proteins, Fusion / metabolism*
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • Receptors, Progesterone / genetics
  • Receptors, Progesterone / metabolism
  • Signal Transduction*
  • Tamoxifen / pharmacology
  • Trans-Activators
  • Transcription, Genetic

Substances

  • Actins
  • Antineoplastic Agents, Hormonal
  • DNA-Binding Proteins
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • MRTFA protein, human
  • Oncogene Proteins, Fusion
  • Receptors, Progesterone
  • Trans-Activators
  • Tamoxifen
  • Estradiol
  • ERBB2 protein, human
  • Receptor, ErbB-2