Is there any association between nek3 and cancers with frequent 13q14 deletion?

Cancer Invest. 2006 Nov;24(7):682-8. doi: 10.1080/07357900600981364.

Abstract

Chromosomal region 13q14 is frequently deleted in prostate cancer. nek3, a protein kinase related gene, is located on this region. Analysis of the coding region of nek3 showed an A insertion/deletion polymorphism in a stretch of adenines at the end of exon 9, with 2 alleles showing either 7 or 8 adenines. In addition we found a variant human NEK3 transcript, which lacks the entire exon 10 due to alternative splicing. The frequency of A8 allele is statistically higher in prostate cancer samples (p < 0.001) than normal controls, indicating that tumor samples preferentially express a full length protein. On the contrary, normal samples have a higher frequency for the A7 allele, expressing preferentially a shorter protein. To test if this association is a common feature in cancers with frequent 13q14 alterations, we analyzed cell lines established from oral, lung, and hepatocellular cancers. An association between nek3 A insertion/deletion polymorphism and cancers with alterations at 13q14 is observed.

MeSH terms

  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / pathology
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 13 / genetics*
  • DNA, Neoplasm / analysis
  • Humans
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / pathology
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / pathology
  • Male
  • NIMA-Related Kinases
  • Polymerase Chain Reaction
  • Prostatic Neoplasms / genetics*
  • Prostatic Neoplasms / pathology
  • Protein Serine-Threonine Kinases / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured

Substances

  • DNA, Neoplasm
  • RNA, Messenger
  • NEK3 protein, human
  • NIMA-Related Kinases
  • Protein Serine-Threonine Kinases