Role of ZNF143 in tumor growth through transcriptional regulation of DNA replication and cell-cycle-associated genes

Cancer Sci. 2010 Dec;101(12):2538-45. doi: 10.1111/j.1349-7006.2010.01725.x. Epub 2010 Sep 23.

Abstract

The cell cycle is strictly regulated by numerous mechanisms to ensure cell division. The transcriptional regulation of cell-cycle-related genes is poorly understood, with the exception of the E2F family that governs the cell cycle. Here, we show that a transcription factor, zinc finger protein 143 (ZNF143), positively regulates many cell-cycle-associated genes and is highly expressed in multiple solid tumors. RNA-interference (RNAi)-mediated knockdown of ZNF143 showed that expression of 152 genes was downregulated in human prostate cancer PC3 cells. Among these ZNF143 targets, 41 genes (27%) were associated with cell cycle and DNA replication including cell division cycle 6 homolog (CDC6), polo-like kinase 1 (PLK1) and minichromosome maintenance complex component (MCM) DNA replication proteins. Furthermore, RNAi of ZNF143 induced apoptosis following G2/M cell cycle arrest. Cell growth of 10 lung cancer cell lines was significantly correlated with cellular expression of ZNF143. Our data suggest that ZNF143 might be a master regulator of the cell cycle. Our findings also indicate that ZNF143 is a member of the growing list of non-oncogenes that are promising cancer drug targets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Line, Tumor
  • Cell Proliferation
  • Cell Separation
  • Chromatin Immunoprecipitation
  • DNA Replication / physiology*
  • Flow Cytometry
  • Gene Expression
  • Gene Expression Regulation, Neoplastic*
  • Genes, cdc*
  • Humans
  • Immunohistochemistry
  • Neoplasms / genetics*
  • Neoplasms / metabolism
  • Oligonucleotide Array Sequence Analysis
  • RNA Interference
  • Trans-Activators / metabolism*

Substances

  • Trans-Activators
  • ZNF143 protein, human