Qualitative and quantitative expression status of the human chromosome 20 genes in cancer tissues and the representative cell lines

J Proteome Res. 2013 Jan 4;12(1):151-61. doi: 10.1021/pr3008336. Epub 2012 Dec 19.


Under the guidance of the Chromosome-centric Human Proteome Project (C-HPP), (1, 2) we conducted a systematic survey of the expression status of genes located at human chromosome 20 (Chr.20) in three cancer tissues, gastric, colon, and liver carcinoma, and their representative cell lines. We have globally profiled proteomes in these samples with combined technology of LC-MS/MS and acquired the corresponding mRNA information upon RNA-seq and RNAchip. In total, 323 unique proteins were identified, covering 60% of the coding genes (323/547) in Chr.20. With regards to qualitative information of proteomics, we overall evaluated the correlation of the identified Chr.20 proteins with target genes of transcription factors or of microRNA, conserved genes and cancer-related genes. As for quantitative information, the expression abundances of Chr.20 genes were found to be almost consistent in both tissues and cell lines of mRNA in all individual chromosome regions, whereas those of Chr.20 proteins in cells are different from tissues, especially in the region of 20q13.33. Furthermore, the abundances of Chr.20 proteins were hierarchically evaluated according to tissue- or cancer-related distribution. The analysis revealed several cancer-related proteins in Chr.20 are tissue- or cell-type dependent. With integration of all the acquired data, for the first time we established a solid database of the Chr.20 proteome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Chromosomes, Human, Pair 20* / genetics
  • Chromosomes, Human, Pair 20* / metabolism
  • Colon / metabolism
  • Colon / pathology
  • Gastric Mucosa / metabolism
  • Gene Expression Regulation, Neoplastic
  • Genome, Human
  • Humans
  • Liver / metabolism
  • Liver / pathology
  • Mass Spectrometry
  • Neoplasms* / genetics
  • Neoplasms* / metabolism
  • Proteins* / classification
  • Proteins* / genetics
  • Proteins* / metabolism
  • Proteome* / genetics
  • Proteome* / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Stomach / pathology


  • Proteins
  • Proteome
  • RNA, Messenger