Cell cycle regulation targets of MYCN identified by gene expression microarrays

Cell Cycle. 2007 May 15;6(10):1249-56. doi: 10.4161/cc.6.10.4222. Epub 2007 May 1.

Abstract

Background: We have previously shown that MYCN knockdown causes a G1 arrest in MYCN amplified (MNA), p53 wild type (wt) and p53 mutant MNA neuroblastoma cell lines, with increases in p21(WAF1) and hypo RB in p53 wt cell lines.

Hypothesis: MYCN acts by inhibiting p21(WAF1), and also by p21(WAF1) independent mechanisms to override the G1 checkpoint in exponentially growing cells.

Methods: Genes potentially regulated by MYCN were identified using gene expression microarrays in p53 wt MNA IMR-32 and p53 mutant MNA SKNBE(2c) neuroblastoma cell lines treated with MYCN or scrambled siRNA. Results were validated using qRT-PCR and confirmed using the regulatable MYCN expression system (SHEP Tet21N).

Results: MYCN knockdown altered the expression of several cell cycle related genes. SKP2 was down regulated in both cell lines, and up regulated in MYCN+ Tet21N cells. Expression of the WNT antagonist DKK3 increased in both cell lines and decreased in MYCN+ Tet21N cells. Expression of CDKN1C (p57(cip2)) and TP53INP1 also increased after MYCN knockdown.

Conclusions: MYCN may override the G1 checkpoint through down-regulation of SKP2 and TP53INP1 resulting in reduced p21(WAF1) expression in p53 wt cell lines, and in addition may act through the WNT signaling pathway in a p53 independent manner.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Blotting, Western
  • Carrier Proteins / metabolism
  • Cell Cycle / physiology*
  • Cell Line, Tumor
  • Chemokines
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism*
  • Gamma Rays
  • Gene Expression Regulation*
  • Heat-Shock Proteins / metabolism
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins / metabolism*
  • Oligonucleotide Array Sequence Analysis
  • Oncogene Proteins / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • S-Phase Kinase-Associated Proteins / metabolism
  • Signal Transduction / genetics*

Substances

  • Adaptor Proteins, Signal Transducing
  • CDKN1A protein, human
  • Carrier Proteins
  • Chemokines
  • Cyclin-Dependent Kinase Inhibitor p21
  • DKK3 protein, human
  • Heat-Shock Proteins
  • Intercellular Signaling Peptides and Proteins
  • MYCN protein, human
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins
  • Oncogene Proteins
  • S-Phase Kinase-Associated Proteins
  • TP53INP1 protein, human