Prolactin signaling and Stat5: going their own separate ways?

Breast Cancer Res. 2002;4(6):209-12. doi: 10.1186/bcr543. Epub 2002 Oct 3.

Abstract

Miyoshi et al. compared the role of the prolactin receptor (PrlR) and its downstream mediator, the signal transducer and activator of transcription 5 (Stat5), in mammary epithelial cells in vivo by studying PrlR-/- and Stat5ab-/- mouse mammary epithelial transplants during pregnancy. At first glance, the two mutant epithelia appear to have similar defects in the differentiation of the alveolar epithelium. However, a closer examination by Miyoshi et al. revealed defects in the epithelial architecture of the smallest ducts of Stat5ab-/- transplants not apparent in the PrlR-/- transplants, suggesting that Stat5 is more than a simple mediator of PrlR action.

Publication types

  • Comment

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Division / drug effects
  • DNA-Binding Proteins / physiology*
  • Estrogens / pharmacology
  • Janus Kinase 2
  • Mammary Glands, Animal / cytology*
  • Mice
  • Mice, Knockout
  • Milk Proteins*
  • Phenotype
  • Progesterone / pharmacology
  • Protein-Tyrosine Kinases / physiology
  • Proto-Oncogene Proteins*
  • Receptors, Prolactin / physiology*
  • STAT5 Transcription Factor
  • Trans-Activators / physiology*

Substances

  • DNA-Binding Proteins
  • Estrogens
  • Milk Proteins
  • Proto-Oncogene Proteins
  • Receptors, Prolactin
  • STAT5 Transcription Factor
  • Trans-Activators
  • Progesterone
  • Protein-Tyrosine Kinases
  • Jak2 protein, mouse
  • Janus Kinase 2