Potential options for managing LOX+ ER- breast cancer patients

Oncotarget. 2016 May 31;7(22):32893-901. doi: 10.18632/oncotarget.9073.

Abstract

Overexpression of lysyl oxidase (LOX) is often observed in estrogen receptor negative (ER-) breast cancer patients with bone metastasis. In the present bioinformatics study, we observed that LOX is a prognostic factor for poor progression free survival in patients with ER- breast cancer. LOX overexpression was positively correlated with resistance to radiation, doxorubin and mitoxantrone, but negatively correlated with resistance to bisphosphonate, PARP1 inhibitors, cisplatin, trabectedin and gemcitabine. LOX overexpression was also associated with EMT and stemness of cancer cells, which leads to chemotherapeutic resistance and poor outcome in ER- patients. Although we suggest several therapeutic interventions that may help in the management of LOX+ ER- breast cancer patients, experiments to validate the function of LOX in ER- breast cancer are still needed.

Keywords: EMT; LOX; bisphosphonates; chemoresistance; estrogen recepter.

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Biomarkers, Tumor / deficiency
  • Biomarkers, Tumor / genetics*
  • Breast Neoplasms / enzymology
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / therapy*
  • Computational Biology
  • Databases, Genetic
  • Diphosphonates / therapeutic use
  • Disease-Free Survival
  • Drug Resistance, Neoplasm
  • Epithelial-Mesenchymal Transition / drug effects
  • Estrogen Receptor alpha / deficiency
  • Estrogen Receptor alpha / genetics*
  • Female
  • Humans
  • Protein-Lysine 6-Oxidase / genetics*
  • Radiation Tolerance
  • Time Factors
  • Treatment Outcome
  • Up-Regulation

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor
  • Diphosphonates
  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Protein-Lysine 6-Oxidase