Discrimination and evaluation of lactoferrin and delta-lactoferrin gene expression levels in cancer cells and under inflammatory stimuli using TaqMan real-time PCR

Esthelle Hoedt, Stephan Hardivillé, Christophe Mariller, E. Elass, Jean Paul Perraudin, Annick Pierce

Research output: Contribution to journalArticle

Abstract

The lactoferrin gene is known to be expressed either constitutively or under inducible conditions such as hormonal stimuli or inflammation. Its transcription from alternative promoters leads to two products, lactoferrin (Lf) and delta-lactoferrin (ΔLf) mRNAs the expressions of which are altered during oncogenesis. The comparison of the two enhancer/promoter regions revealed that the two isoforms might be differentially trans-activated. Nevertheless, concomitant expression of both transcripts has been found in some normal tissues and in a subset of breast cancer cell lines and biopsies. Moreover, we found putative inflammatory response elements in both P1 and P2 promoter regions suggesting that both Lf and ΔLf might be upregulated under inflammatory stimuli. Therefore, a duplex Taqman gene expression assay has been developed and used to profile mRNA expression of the Lf gene in the case of cancer and under inflammatory conditions. Discrimination between the two transcripts is achieved by using a primer pairs/probe set within exon 1β for ΔLf and a primer pairs/probe set within exon 1 and exon 2 for Lf. In this study, we confirmed that Lf/ΔLf Taqman gene expression assay is a powerful tool to investigate the expression of both Lf and ΔLf transcripts. We also showed that lymphocytes and leukocytes isolated from fresh human blood expressed an extremely high level of ΔLf messengers. An extensive series of cancer cell lines has been studied confirming that both P1 and P2 promoter regions of the Lf gene are downregulated or silenced in the case of cancer. Furthermore, using stimulation by bacterial lipopolysaccharides (LPS), we showed that in MDA-MB-231 and HT-29 epithelial cells, Lf expression is strongly increased with a higher expression level in MDA-MB-231 whereas ΔLf expression is not. These results suggest that the NF-κB/cRel response elements present in the P1 promoter region are functional whereas those present in the P2 promoter region are not and show that ΔLf is not regulated in inflammatory conditions.

Original languageEnglish (US)
Pages (from-to)441-452
Number of pages12
JournalBioMetals
Volume23
Issue number3
DOIs
StatePublished - Jun 1 2010

Keywords

  • Cancer
  • Delta-lactoferrin
  • LPS
  • Lactoferrin
  • Q-PCR
  • TaqMan real-time PCR

ASJC Scopus subject areas

  • Biomaterials
  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • Metals and Alloys

Fingerprint Dive into the research topics of 'Discrimination and evaluation of lactoferrin and delta-lactoferrin gene expression levels in cancer cells and under inflammatory stimuli using TaqMan real-time PCR'. Together they form a unique fingerprint.

  • Cite this