HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Lineage-specific silencing of human IL-10 gene expression by promoter methylation in cervical cancer cells.

Abstract
Epigenetic analysis was performed to demonstrate that the normal and neoplastic epithelial cells do not serve as the source of the locally elevated IL-10 production during cervical carcinogenesis. Bisulfite sequencing was used to correlate promoter CpG methylation with the transcription of the gene. Lack of IL-10 transcription in HeLa, SiHa, Caski, HT-3, C33-A, HaCaT cell lines and in primary human keratinocytes correlated consistently with the methylated state of the proximal CpG residues, particularly with the two most proximal CpGs at positions -185 and -110. These two sites were also highly methylated in normal and malignant cervical cells directly isolated from patient material. On the other hand, IL-10 producing peripheral blood mononuclear cells had unmethylated CpG residues in the proximal promoter associated with acetylated H3 and H4 histones as determined by chromatin immunoprecipitation. In HeLa carrying epigenetically silenced endogeneous IL-10 promoter, the transfected non-CpG methylated 1 kb and 0.6 kb proximal promoter fragments could drive reporter gene expression, which was reversed by cassette methylation of these promoter fragments. In conclusion, the CpG methylation pattern of the proximal promoter is implicated as a major determinant of transcriptional silencing of human IL-10 expression in cells of cervical epithelial origin.
AuthorsAnita Szalmás, Ferenc Bánáti, Anita Koroknai, Brigitta László, Eniko Fehér, Dániel Salamon, Lajos Gergely, János Minárovits, József Kónya
JournalEuropean journal of cancer (Oxford, England : 1990) (Eur J Cancer) Vol. 44 Issue 7 Pg. 1030-8 (May 2008) ISSN: 0959-8049 [Print] England
PMID18378443 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Interleukin-10
  • Histone Acetyltransferases
Topics
  • Cell Line, Tumor
  • DNA Methylation
  • Female
  • Gene Expression (genetics)
  • Gene Silencing
  • Histone Acetyltransferases (metabolism)
  • Humans
  • Interleukin-10 (genetics)
  • Keratinocytes (metabolism)
  • Promoter Regions, Genetic (genetics)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Uterine Cervical Neoplasms (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: