Prokineticin 1 mRNA expression in the endometrium of healthy women and in the eutopic endometrium of women with endometriosis

Fertil Steril. 2010 May 1;93(7):2145-9. doi: 10.1016/j.fertnstert.2009.01.105. Epub 2009 Mar 14.

Abstract

Objective: To examine prokineticin 1 (PROK1) mRNA expression in eutopic endometrial glands obtained from patients with or without endometriosis, to investigate the presence of additional endometrial abnormalities in women with endometriosis.

Design: Prospective laboratory study.

Setting: University hospital.

Patients: Twelve control women and 12 patients affected by endometriosis in the secretory phase of the menstrual cycle.

Intervention(s): Endometrial specimens were obtained from women affected (cases) or not (control group) by endometriosis. Endometrial glands were freshly isolated from endometrial biopsies.

Main outcome measure(s): PROK1 mRNA expression levels by real-time polymerase chain reaction analysis.

Results: PROK1 mRNA was detectable in 4 of 12 (33%) samples obtained from women affected by endometriosis, whereas 10 of 12 (83%) samples obtained from normal women were positive for PROK1 detection by real-time polymerase chain reaction. Moreover, detectable PROK1 mRNA levels were 10 times lower in samples obtained from women with endometriosis than in samples obtained from control women.

Conclusion(s): PROK1 is a newly discovered angiogenic factor implicated in the vascular function of peri-implantation endometrium and early pregnancy. An altered expression of PROK1 could be one of the several biochemical abnormalities characterizing eutopic endometrium in endometriosis.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Biopsy
  • Endometriosis / genetics*
  • Endometriosis / metabolism
  • Endometriosis / pathology
  • Endometrium / metabolism*
  • Endometrium / pathology
  • Female
  • Health
  • Humans
  • Luteal Phase / genetics
  • Luteal Phase / metabolism
  • RNA, Messenger / metabolism
  • Uterine Diseases / genetics*
  • Uterine Diseases / metabolism
  • Uterine Diseases / pathology
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived / genetics*
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived / metabolism

Substances

  • RNA, Messenger
  • Vascular Endothelial Growth Factor, Endocrine-Gland-Derived