Molecular events underlying pregnancy-induced cardiomyopathy

Cell. 2007 Feb 9;128(3):437-8. doi: 10.1016/j.cell.2007.01.020.

Abstract

The etiology of cardiomyopathy in pregnant women remains unclear. In this issue, Hilfiker-Kleiner et al. (2007) report that a reduction in STAT3 and a concomitant increase in cathepsin D may be a cause of this disease. Cathepsin D generates an antiangiogenic cleavage product of the hormone prolactin. The authors show that an inhibitor of prolactin secretion may be useful in treating this disease.

Publication types

  • Comment

MeSH terms

  • Animals
  • Bromocriptine / therapeutic use
  • Cardiomyopathies / drug therapy
  • Cardiomyopathies / metabolism*
  • Cathepsin D / metabolism*
  • Disease Models, Animal
  • Female
  • Humans
  • Pregnancy
  • Pregnancy Complications, Cardiovascular / metabolism*
  • Prolactin / antagonists & inhibitors
  • Prolactin / metabolism*
  • Puerperal Disorders / drug therapy
  • Puerperal Disorders / metabolism*
  • STAT3 Transcription Factor / metabolism*

Substances

  • STAT3 Transcription Factor
  • Bromocriptine
  • Prolactin
  • Cathepsin D