Expression of interleukin-8 and monocyte chemotactic protein-1 in adenomyosis

Hum Reprod. 2005 Oct;20(10):2958-63. doi: 10.1093/humrep/dei154. Epub 2005 Jun 24.

Abstract

Background: To clarify the inflammatory nature of adenomyosis, we aimed to investigate the expression of interleukin-8 (IL-8) and monocyte chemotactic protein-1 (MCP-1) by immunohistochemistry to determine their putative role in pathophysiology of adenomyosis.

Methods: Adenomyosis samples, with their eutopic endometrium, were collected from 30 women undergoing hysterectomy. Endometrium from 27 women without adenomyosis were also collected as a control group. Samples were grouped according to the menstrual cycle phase and examined by immunohistochemistry for IL-8 and MCP-1.

Results: In normal endometrium, secretory phase samples expressed higher levels of epithelial IL-8 than in proliferative phase samples (P = 0.01), and we observed a trend for an increased epithelial MCP-1 expression in the secretory phase samples compared with the proliferative phase samples (P = 0.07). Endometrial samples of women with adenomyosis did not show the same cyclic variation. In the secretory phase, eutopic endometrium of women with adenomyosis expressed lower levels of epithelial IL-8 and MCP-1 compared with normal endometrium (P < 0.05). The expression of epithelial IL-8 and MCP-1 was higher in the adenomyosis foci than the eutopic endometrium (P < 0.05).

Conclusions: These findings may indicate that an intrinsic abnormality of inflammatory response may be present in eutopic endometrium of women with adenomyosis, and IL-8 and MCP-1 may contribute to the pathophysiology of adenomyosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Chemokine CCL2 / biosynthesis*
  • Endometriosis / metabolism*
  • Endometrium / metabolism
  • Endometrium / pathology
  • Female
  • Gene Expression Regulation*
  • Humans
  • Hysterectomy
  • Immunohistochemistry
  • Inflammation
  • Interleukin-8 / biosynthesis*
  • Interleukin-8 / metabolism
  • Middle Aged
  • Retrospective Studies
  • Time Factors

Substances

  • Chemokine CCL2
  • Interleukin-8