Single-Cell Transcriptome Analysis Reveals Estrogen Signaling Coordinately Augments One-Carbon, Polyamine, and Purine Synthesis in Breast Cancer

Cell Rep. 2018 Nov 20;25(8):2285-2298.e4. doi: 10.1016/j.celrep.2018.10.093.

Abstract

Estrogen drives breast cancer (BCa) progression by directly activating estrogen receptor α (ERα). However, because of the stochastic nature of gene transcription, it is important to study the estrogen signaling pathway at the single-cell level to fully understand how ERα regulates transcription. Here, we performed single-cell transcriptome analysis on ERα-positive BCa cells following 17β-estradiol stimulation and reconstructed the dynamic estrogen-responsive transcriptional network from discrete time points into a pseudotemporal continuum. Notably, differentially expressed genes show an estrogen-stimulated metabolic switch that favors biosynthesis but reduces estrogen degradation. Moreover, folate-mediated one-carbon metabolism is reprogrammed through the mitochondrial folate pathway and polyamine and purine synthesis are upregulated coordinately. Finally, we show AZIN1 and PPAT are direct ERα targets that are essential for BCa cell survival and growth. In summary, our study highlights the dynamic transcriptional heterogeneity in ERα-positive BCa cells upon estrogen stimulation and uncovers a mechanism of estrogen-mediated metabolic switch.

Keywords: breast cancer; estrogen receptor α; metabolic switch; single-cell RNA sequencing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / genetics*
  • Breast Neoplasms / metabolism
  • Carbon / metabolism*
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Estrogens / biosynthesis
  • Estrogens / metabolism*
  • Estrogens / pharmacology
  • Female
  • Folic Acid / metabolism
  • Gene Expression Profiling*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • MCF-7 Cells
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Polyamines / metabolism*
  • Purines / metabolism*
  • Signal Transduction*
  • Single-Cell Analysis*
  • Time Factors

Substances

  • Estrogens
  • Polyamines
  • Purines
  • Carbon
  • Folic Acid
  • purine