Calcipotriol affects keratinocyte proliferation by decreasing expression of early growth response-1 and polo-like kinase-2

Pharm Res. 2008 Mar;25(3):521-9. doi: 10.1007/s11095-007-9388-z. Epub 2007 Aug 2.

Abstract

Purpose: Calcipotriol is a potent drug for topical treatment of psoriasis because it manages to inhibit keratinocyte proliferation. In the present study we investigated the effects of calcipotriol on gene expression in human keratinocytes in terms of mechanism of how calcipotriol decreases proliferation.

Materials and methods: Cell proliferation was analyzed by MTT assay. The differential display approach together with qPCR was used to assess the gene expression after treatment. In addition, Western immunoblotting revealed differences on the protein level. Finally, transfection of the KCs with specific small interfering RNA determined the genes necessary to inhibit proliferation.

Results: KCs proliferation was decreased in a concentration-dependent manner. Moreover, calcipotriol dowregulated the expression of two proliferation factors: early growth response-1 (EGR1) and polo-like kinase-2 (PLK2). The protein levels of EGR1 and PLK2 were also decreased. Specific siRNA against EGR1 and PLK2 in KCs resulted in marked reduction of EGR1 and PLK2 expression. In both cases, the reduction resolved in the decreased proliferation of KCs.

Conclusion: This study provides a new insight into how calcipotriol affects proliferation of keratinocytes by decreasing the expression of EGR1 and PLK2. Furthermore, the results offer groundwork for developing novel compounds for the treatment of hyperproliferative skin disorders like psoriasis.

MeSH terms

  • Blotting, Western
  • Calcitriol / analogs & derivatives*
  • Calcitriol / pharmacology
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Dermatologic Agents / pharmacology*
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Early Growth Response Protein 1 / genetics
  • Early Growth Response Protein 1 / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation, Enzymologic / drug effects*
  • Humans
  • Keratinocytes / drug effects*
  • Keratinocytes / enzymology
  • Keratinocytes / metabolism
  • Polo-Like Kinase 1
  • Polymerase Chain Reaction
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • RNA Interference
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Transfection

Substances

  • Cell Cycle Proteins
  • Dermatologic Agents
  • EGR1 protein, human
  • Early Growth Response Protein 1
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • calcipotriene
  • Protein Serine-Threonine Kinases
  • Calcitriol