An estrogen receptor (ER)-related signature in predicting prognosis of ER-positive breast cancer following endocrine treatment

J Cell Mol Med. 2019 Aug;23(8):4980-4990. doi: 10.1111/jcmm.14338. Epub 2019 May 23.

Abstract

Quite a few estrogen receptor (ER)-positive breast cancer patients receiving endocrine therapy are at risk of disease recurrence and death. ER-related genes are involved in the progression and chemoresistance of breast cancer. In this study, we identified an ER-related gene signature that can predict the prognosis of ER-positive breast cancer patient receiving endocrine therapy. We collected RNA expression profiling from Gene Expression Omnibus database. An ER-related signature was developed to separate patients into high-risk and low-risk groups. Patients in the low-risk group had significantly better survival than those in the high-risk group. ROC analysis indicated that this signature exhibited good diagnostic efficiency for the 1-, 3- and 5-year disease-relapse events. Moreover, multivariate Cox regression analysis demonstrated that the ER-related signature was an independent risk factor when adjusting for several clinical signatures. The prognostic value of this signature was validated in the validation sets. In addition, a nomogram was built and the calibration plots analysis indicated the good performance of this nomogram. In conclusion, combining with ER status, our results demonstrated that the ER-related prognostic signature is a promising method for predicting the prognosis of ER-positive breast cancer patients receiving endocrine therapy.

Keywords: breast cancer; estrogen receptor; nomogram; prognosis.

Publication types

  • Validation Study

MeSH terms

  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology*
  • Databases, Genetic
  • Estrogens / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Middle Aged
  • Neoplasm Recurrence, Local / genetics*
  • Prognosis
  • Proportional Hazards Models
  • ROC Curve
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Regression Analysis
  • Risk Factors
  • Transcriptome / genetics

Substances

  • Estrogens
  • Receptors, Estrogen