DNA repair pathway profiling and microsatellite instability in colorectal cancer

Jinsheng Yu, Mary A. Mallon, Wanghai Zhang, Robert Freimuth, Sharon Marsh, Mark A. Watson, Paul J. Goodfellow, Howard L. McLeod

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Background: The ability to maintain DNA integrity is a critical cellular function. DNA repair is conducted by distinct pathways of genes, many of which are thought to be altered in colorectal cancer. However, there has been little characterization of these pathways in colorectal cancer. Method: By using the TaqMan real-time quantitative PCR, RNA expression profiling of 20 DNA repair pathway genes was done in matched tumor and normal tissues from 52 patients with Dukes'C colorectal cancer. Results: The relative mRNA expression level across the 20 DNA repair pathway genes varied considerably, and the individual variability was also quite large, with an 85.4 median fold change in the tumor tissue genes and a 127.2 median fold change in the normal tissue genes. Tumor-normal differential expression was found in 13 of 20 DNA repair pathway genes (only XPA had a lower RNA level in the tumor samples; the other 12 genes had significantly higher tumor levels, all P < 0.01). Coordinated expression of ERCC6, HMG1 MSH2, and POLB (Rs ≥ 0.60) was observed in the tumor tissues (all P < 0.001). Apoptosis index was not correlated with expression of the 20 DNA repair pathway genes. MLH1 and XRCC1 RNA expression was correlated with microsatellite instability status (P = 0.045 and 0.020, respectively). An inverse correlation was found between tumor MLH1 RNA expression and MLH1 DNA methylation (P = 0.003). Conclusion: Our study provides an initial characterization of the DNA repair pathways for understanding the cellular DNA damage/repair system in human colorectal cancer.

Original languageEnglish (US)
Pages (from-to)5104-5111
Number of pages8
JournalClinical Cancer Research
Volume12
Issue number17
DOIs
StatePublished - Sep 1 2006
Externally publishedYes

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Microsatellite Instability
DNA Repair
Colorectal Neoplasms
Genes
Neoplasms
RNA
HMGB1 Protein
DNA Methylation
DNA Damage
Real-Time Polymerase Chain Reaction
Apoptosis
Messenger RNA
DNA

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Yu, J., Mallon, M. A., Zhang, W., Freimuth, R., Marsh, S., Watson, M. A., ... McLeod, H. L. (2006). DNA repair pathway profiling and microsatellite instability in colorectal cancer. Clinical Cancer Research, 12(17), 5104-5111. https://doi.org/10.1158/1078-0432.CCR-06-0547

DNA repair pathway profiling and microsatellite instability in colorectal cancer. / Yu, Jinsheng; Mallon, Mary A.; Zhang, Wanghai; Freimuth, Robert; Marsh, Sharon; Watson, Mark A.; Goodfellow, Paul J.; McLeod, Howard L.

In: Clinical Cancer Research, Vol. 12, No. 17, 01.09.2006, p. 5104-5111.

Research output: Contribution to journalArticle

Yu, J, Mallon, MA, Zhang, W, Freimuth, R, Marsh, S, Watson, MA, Goodfellow, PJ & McLeod, HL 2006, 'DNA repair pathway profiling and microsatellite instability in colorectal cancer', Clinical Cancer Research, vol. 12, no. 17, pp. 5104-5111. https://doi.org/10.1158/1078-0432.CCR-06-0547
Yu, Jinsheng ; Mallon, Mary A. ; Zhang, Wanghai ; Freimuth, Robert ; Marsh, Sharon ; Watson, Mark A. ; Goodfellow, Paul J. ; McLeod, Howard L. / DNA repair pathway profiling and microsatellite instability in colorectal cancer. In: Clinical Cancer Research. 2006 ; Vol. 12, No. 17. pp. 5104-5111.
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