Network-based approach reveals Y chromosome influences prostate cancer susceptibility

Comput Biol Med. 2014 Nov:54:24-31. doi: 10.1016/j.compbiomed.2014.08.020. Epub 2014 Aug 26.

Abstract

The human Y chromosome contains a small number of genes that play a critical role in the determination of male-specific organs. Today's advances have provided valuable resources for defining the functions of this chromosome in both normal and cancerous prostates. Despite the fact that generation of high-throughput expression data is becoming usual; the systematic methods of data analysis in a biological context are still an impediment. Here we have shown that constructing co-expression networks using Y-chromosome genes provides an alternative strategy for the detection of new candidate genes involved in prostate cancer. In our approach, independent co-expression networks from normal and cancerous stages are reconstructed using a reverse engineering approach. We then highlight crucial pathways, biological processes, and genes involved in the prostate cancer by analyzing each network individually and in concert. Thus, we have identified 18 critical pathways and processes related to prostate cancer, many of which have previously been shown to be involved in cancer. In particular, we identify 22 Y-chromosome genes putatively linked to prostate cancer, 13 of which have been already verified experimentally. Our novel network-based approach is useful for accurate inference of processes and essential regulators that mediate molecular changes during cancer progression.

Keywords: Co-expression networks; Expression data; Prostate cancer; Reverse engineering approach; Y-chromosome genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Y / genetics*
  • Computer Simulation
  • Gene Expression Regulation, Neoplastic / genetics
  • Genes, Neoplasm / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Humans
  • Male
  • Models, Genetic*
  • Neoplasm Proteins / genetics*
  • Prostatic Neoplasms / genetics*
  • Signal Transduction / genetics*

Substances

  • Neoplasm Proteins