Overexpression of cyclin E protein is closely related to the mutator phenotype of colorectal carcinoma

Int J Colorectal Dis. 2002 Nov;17(6):374-80. doi: 10.1007/s00384-002-0390-y. Epub 2002 Mar 8.

Abstract

Background and aims: A subset of colorectal carcinomas are due to a deficiency in the DNA mismatch repair system. The molecular mechanisms of tumorigenesis in these tumors is not yet well understood. Deregulation of the cell cycle, specifically of the G(1) and S phases, is a hallmark of human cancers. Transition from the G(1) to the S phase is accelerated by increased cyclin E protein expression, and recent studies suggest that overexpression of cyclin E leads to chromosomal instability. The overexpression of cyclin E in a variety of human cancers, for example in colorectal, gastric, lung, breast, and kidney cancer, provides evidence that cyclin E plays a pivotal role in the cell cycle and replication. We examined whether the overexpression of cyclin E is related to the status of the mismatch repair system in colorectal carcinomas.

Patients and methods: Frozen tumor samples and adjacent normal colon mucosa obtained from 100 patients were subjected to microsatellite analysis, RT-PCR, western blot analysis and immunohistochemistry.

Results: High microsatellite instability was detected in 13 tumors, and in 10 of these (77%) cyclin E protein was overexpressed at least twofold compared to normal mucosa. In contrast, only 28 of the remaining 87 microsatellite stable tumors (32%) overexpressed cyclin E. Lower molecular weight cyclin E proteins were present in 7 of 87 microsatellite stable carcinoma (8%), compared to 7 cases exhibiting lower molecular weight isoforms of 13 MSI carcinoma (54%).

Conclusion: Increased cyclin E protein expression and the appearance of lower molecular weight cyclin E proteins were significantly associated with MSI in colorectal tumors. The data indicate that increased and/or aberrant expression of cyclin E protein might contribute to the mutator phenotype of colorectal cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism*
  • Cyclin E / biosynthesis*
  • Cyclin E / genetics
  • DNA, Neoplasm / analysis
  • Gene Expression
  • Genetic Markers
  • Humans
  • Immunohistochemistry
  • Microsatellite Repeats
  • Molecular Weight
  • Mutation*
  • Phenotype
  • Polymerase Chain Reaction
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Tumor Cells, Cultured

Substances

  • Cyclin E
  • DNA, Neoplasm
  • Genetic Markers
  • Protein Isoforms
  • RNA, Messenger