Inflammation-related gene expression profiles of endocervical polyps

J Interferon Cytokine Res. 2012 May;32(5):191-7. doi: 10.1089/jir.2011.0066. Epub 2012 Apr 2.

Abstract

The roles of inflammation-associated genes in the pathogenesis of endocervical polyps remain unclear. We thus compared the expression levels of 509 inflammation-associated genes between endocervical polyp tissues and endocervical canal membrane tissues using a gene microarray. Sixteen inflammation-related genes were differentially expressed in endocervical polyps compared with those of normal endocervical canal membrane tissues. Expression of 8 of these 16 genes was further validated biochemically. The protein expression levels of IL-12P40, IL-17, IFN-γ, TNF-α, CCR2, and IL-11 were significantly higher in endocervical polyps than those in endocervical canal tissues, while expression of TGF-β1 and IL-10 was significantly lower (P<0.05). In addition, endocervical polyp tissues expressed IL-12P40, IL-17, IFN-γ, TNF-α, CCR2, IL-11, TGF-β1, and IL-10 mainly in the cytoplasm of the inflammatory cells and, to a lesser extent, in the acinus of the serous gland. Endocervical polyp is a polygenic disease and aberrantly expressed genes may play roles in its pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Cervix Uteri / immunology*
  • Cytokines / genetics*
  • Cytokines / immunology
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Inflammation / genetics*
  • Inflammation Mediators / immunology
  • Microarray Analysis
  • Middle Aged
  • Polyps / genetics*
  • Polyps / immunology
  • Receptors, Cytokine / genetics
  • Receptors, Cytokine / metabolism
  • Uterine Cervical Neoplasms / genetics
  • Uterine Cervical Neoplasms / immunology
  • Young Adult

Substances

  • Cytokines
  • Inflammation Mediators
  • Receptors, Cytokine