The effect of bisphosphonates on gene expression: GAPDH as a housekeeping or a new target gene?

BMC Cancer. 2006 Mar 3:6:49. doi: 10.1186/1471-2407-6-49.

Abstract

Background: RT-PCR has been widely used for the analysis of gene expression in many systems, including tumor samples. GAPDH (Glyceraldehyde-3-phosphate dehydrogenase) has been frequently considered as a constitutive housekeeping gene and used to normalize changes in specific gene expression. However, GAPDH has been shown to be up-regulated in many cancers and down-regulated by chemotherapic drugs. Bisphosphonates, potent inhibitors of bone resorption, have recently shown a direct and indirect antitumor effect in vitro and in animal models. They exert their effects mainly by inhibiting the mevalonate pathway but also by modulating the expression of many genes not only in osteoclasts but also in cancer cells.

Methods: We evaluated GAPDH gene expression by real time RT PCR in breast (MCF-7 and T47D) and prostate (PC3 and DU-145) cancer cell lines treated with amino and non-amino bisphosphonates.

Results: Our results showed that amino-bisphosphonates significantly decrease in a dose-dependent manner the expression of GAPDH gene.

Conclusion: Therefore, GAPDH is inaccurate to normalize mRNA levels in studies investigating the effect of bisphosphonates on gene expression and it should be avoided. On the other hand, this gene could be considered a potential target to observe the effects of bisphosphonates on cancer cells.

MeSH terms

  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Diphosphonates / pharmacology*
  • Dose-Response Relationship, Drug
  • Female
  • Gene Expression Profiling
  • Genetic Markers
  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) / biosynthesis*
  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) / genetics*
  • Humans
  • Male
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / pathology
  • RNA, Messenger / analysis
  • Reference Values
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Cells, Cultured
  • Up-Regulation

Substances

  • Diphosphonates
  • Genetic Markers
  • RNA, Messenger
  • Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+)