Cancer stem-like properties of hormonal therapy-resistant breast cancer cells

Breast Cancer. 2019 Jul;26(4):459-470. doi: 10.1007/s12282-018-00944-1. Epub 2019 Jan 4.

Abstract

Background: Presently, hormonal therapy targeting estrogen receptors is the most effective treatment available for luminal breast cancer. However, many patients relapse after the therapy. It has been suggested that cancer stem-like cells are involved with hormonal therapy resistance; in the present study, we evaluated this hypothesis.

Methods: In the present study, we used our previously established hormonal therapy-resistant cell lines, including aromatase inhibitor (AI)-resistant cells (Type 1 and Type 2) and fulvestrant-resistant cells (MFR).

Results: AI-resistant cell lines expressing ER (Type 1 V1 and V2) showed high cancer stemness in terms of their CD44/CD24 expression and side populations, which were stimulated by the addition of estrogen and inhibited by fulvestrant. However, ALDH activity was lower than in the ER-negative resistant cells, suggesting that the stemness of luminal cells is distinct from that of basal-like breast cancer cells. The migration and invasion activity of the ER-positive Type 1 V1 and V2 cells were higher than in the ER-negative cell lines, Type 2 and MFR.

Conclusions: Fractionation of parental cells based on CD44/CD24 expression and colony formation assay indicated that CD44+/CD24+ cells might be the origin of hormonal therapy-resistant cells. This population reconstituted various other subpopulations under estrogen deprivation. These results indicate that hormonal therapy resistance is closely related to the cancer stem cell-like properties of luminal breast cancer.

Keywords: Breast cancer; Cancer stem-like cells; Estrogen receptor; Hormonal therapy resistance.

MeSH terms

  • Antineoplastic Agents, Hormonal / pharmacology*
  • Aromatase Inhibitors / pharmacology
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • CD24 Antigen / metabolism
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm / drug effects
  • Drug Resistance, Neoplasm / genetics
  • Estradiol / metabolism
  • Estrogen Receptor Antagonists / pharmacology
  • Female
  • Fulvestrant
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Hyaluronan Receptors / metabolism
  • MCF-7 Cells
  • Neoplastic Stem Cells / pathology
  • Receptors, Estrogen / metabolism

Substances

  • Antineoplastic Agents, Hormonal
  • Aromatase Inhibitors
  • CD24 Antigen
  • CD24 protein, human
  • CD44 protein, human
  • Estrogen Receptor Antagonists
  • Hyaluronan Receptors
  • Receptors, Estrogen
  • Fulvestrant
  • Estradiol