Quantification of PRL/Stat5 signaling with a novel pGL4-CISH reporter

BMC Biotechnol. 2008 Feb 6:8:11. doi: 10.1186/1472-6750-8-11.

Abstract

Background: Elevations of serum prolactin (PRL) are associated with an increased risk for breast cancer. PRL signaling through its prolactin receptor (PRLr) involves the Jak2/Stat5 pathway. Luciferase-based reporter assays have been widely used to evaluate the activity of this pathway. However, the existing reporters are often not sensitive enough to monitor the effect of PRL in this pathway.

Results: In this study, a new biologically relevant reporter, pGL4-CISH, was generated to study the PRL/Jak2/Stat5 signaling pathway. The sensitivity of pGL4-CISH to detect PRL was superior to that of several other commonly utilized Stat5-responsive reporters. Interestingly, the enhanced function pGL4-CISH was restricted to the estrogen receptor positive (ER+) human breast cancer cell lines T47D and MCF7, but not in the ER-MDA-231, BT-474, or MCF10A cell lines. Overexpression of Stat5 further enhanced the effect of PRL on pGL4-CISH.

Conclusion: These studies demonstrate that pGL4-CISH is a novel and sensitive reporter for assessing the activity of the PRL/Stat5 signaling pathway in the ER+ human breast cancer cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Cell Line, Tumor
  • Gene Expression Profiling / methods*
  • Genes, Reporter / genetics
  • Humans
  • Prolactin / metabolism*
  • Receptors, Estrogen / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • STAT5 Transcription Factor / metabolism*
  • Signal Transduction*
  • Suppressor of Cytokine Signaling Proteins / genetics
  • Suppressor of Cytokine Signaling Proteins / metabolism*

Substances

  • Receptors, Estrogen
  • Recombinant Fusion Proteins
  • STAT5 Transcription Factor
  • Suppressor of Cytokine Signaling Proteins
  • cytokine inducible SH2-containing protein
  • Prolactin