Cancer-related SRCAP and TPR mutations in colon cancers

Pathol Res Pract. 2021 Jan:217:153292. doi: 10.1016/j.prp.2020.153292. Epub 2020 Nov 23.

Abstract

Current information suggests that SRCAP, TPR and CEACAM5 genes have cancer-related activities, but their alteration status is not well identified in colon cancer (CC). In this study, we analyzed frameshift mutations of these genes in CCs according to the microsatellite instability (MSI) status (high MSI (MSI-H) and microsatellite stable (MSS) CCs). In addition, regional difference in frameshift mutations of SRCAP, TPR and CEACAM5 genes were studied in CCs. In this study, we detected frameshift mutations (deletion or duplication of one or two bases) of SRCAP in 12 (12 %), TPR in 3 (3%) and CEACAM5 in 2 (2%) CCs with MSI-H. However, there was no such mutations in MSS cancers (P < 0.001). 18.8 % and 6.3 % of 16 CCs showed the regional difference in the SRCAP and TPR mutations, respectively. Approximately in 60 % of the CCs, SRCAP expression was increased compared to normal colon cells. Our study shows that SRCAP, TPR and CEACAM5 frameshift mutations and their regional difference as well as altered SRCAP expression are present in MSI-H CCs, which could contribute to CC development with MSI-H.

Keywords: Colon cancer; Expression; Mutation; Regional difference.

Publication types

  • Comparative Study

MeSH terms

  • Adenosine Triphosphatases / analysis
  • Adenosine Triphosphatases / genetics*
  • Biomarkers, Tumor / analysis
  • Biomarkers, Tumor / genetics*
  • Carcinoembryonic Antigen / genetics
  • Colonic Neoplasms / enzymology
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / pathology
  • Frameshift Mutation*
  • GPI-Linked Proteins / genetics
  • Genetic Predisposition to Disease
  • Humans
  • Microsatellite Instability
  • Nuclear Pore Complex Proteins / genetics*
  • Phenotype
  • Proto-Oncogene Proteins / genetics*

Substances

  • Biomarkers, Tumor
  • CEACAM5 protein, human
  • Carcinoembryonic Antigen
  • GPI-Linked Proteins
  • Nuclear Pore Complex Proteins
  • Proto-Oncogene Proteins
  • TPR protein, human
  • Adenosine Triphosphatases
  • SRCAP protein, human