Dissecting the genetic basis of Rheumatiod Arthritis in mouse models

Saleh M. Ibrahim, Xinhua Yu

Research output: Contribution to journalReview articlepeer-review

9 Scopus citations

Abstract

Rheumatoid Arthritis, RA, is a common polygenic multi-factorial chronic inflammatory disorder that involves complex interactions between genetic and environmental factors. Despite major advances, the aetiology of the disease is still not completely understood. In this post-genome era, the sequencing of the human and some murine genomes as well as advances in global screening technologies offer an opportunity to accelerate the search for new pathological pathways and to identify new therapeutic targets. Animal models of RA offer an opportunity to dissect the genetic basis of disease in a simplified genome and controlled environment with the aim of identifying new pathological pathways and thus new therapeutic targets. Linkage analysis in the mouse model has identified more than 60 Loci, controlling disease phenotypes, immune response and cytokines. This indicates that gene variations among inbred mice strains affect the disease and that those polymorphic genes could be potential therapeutic targets. However, progress in identification of susceptibility genes in mouse models is slow. The progress is hampered by the complexity of disease as well as the traditional genetic dissection strategies. In this post-genome era, the sequencing of the human and some murine genomes as well as advances in global screening technologies offer an opportunity to accelerate the progress.

Original languageBritish English
Pages (from-to)3753-3759
Number of pages7
JournalCurrent Pharmaceutical Design
Volume12
Issue number29
DOIs
StatePublished - Oct 2006

Keywords

  • Collagen induced arthritis
  • Epistasis
  • Genomics
  • Microarrays
  • Quantitative trait loci
  • Rheumatoid arthritis

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