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Epigenetic-Genetic Interactions in the<i>APC/WNT, RAS/RAF</i>, and<i>P53</i>Pathways in Colorectal Carcinoma

Yutaka Suehiro, Chi Wai Wong, Lucian R. Chirieac, Yutaka Kondo, Lanlan Shen, C. Renee Webb, Yee Wai Chan, Annie S Y Chan, Tsun Leung Chan, Tsung‐Teh Wu, Asif Rashid, Yuichiro Hamanaka, Yuji Hinoda, Rhonda L. Shannon, Xuemei Wang

Clinical Cancer Research · 2008 · ▲ 102 citations

Abstract

PURPOSE: Early events in colorectal tumorigenesis include mutation of the adenomatous polyposis coli (APC) gene and epigenetic hypermethylation with transcriptional silencing of the O(6)-methylguanine DNA methyltransferase (MGMT), human mut L homologue 1 (hMLH1), and P16/CDKN2A genes. Epigenetic alterations affect genetic events: Loss of MGMT via hypermethylation reportedly predisposes to guanine-to-adenine or cytosine-to-thymine (G:C-->A:T) transition mutations in KRAS and P53, and silencing of hMLH1 leads to high levels of microsatellite instability (MSI-H)/mutator phenotype, suggesting that epigenetic-genetic subtypes exist. EXPERIMENTAL DESIGN: We evaluated the relationships of aberrant methylation of APC, MGMT, hMLH1, P16, N33, and five MINTs to mutations in APC, KRAS, BRAF, and P53 in 208 colorectal carcinomas. RESULTS: We found that APC hypermethylation was age related (P = 0.04), in contrast to the other genes, and did not cluster with CpG island methylator phenotype (CIMP) markers. Hypermethylation of APC concurrently with either MGMT or hMLH1 was strongly associated with occurrence of G-to-A transitions in APC [odds ratio (OR), 26.8; P < 0.0002 from multivariable logic regression model], but C-to-T transitions had no associations. There was no relationship of hypermethylation of any gene, including MGMT, with G-to-A or C-to-T transitions in KRAS or P53, although APC hypermethylation was associated with P53 mutation (P < 0.0002). CIMP with MSI-H due to hMLH1 hypermethylation, or CIMP with loss of MGMT expression in non-MSI-H tumors, was associated with BRAF mutation (OR, 4.5; P < 0.0002). CIMP was also associated with BRAF V600E T-to-A transversion (OR, 48.5; P < 0.0002). CONCLUSIONS: Our findings suggest that the heterogeneous epigenetic dysregulation of promoter methylation in various genes is interrelated with the occurrence of mutations, as manifested in epigenetic-genetic subgroups of tumors.

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OpenAlex
DOI
10.1158/1078-0432.ccr-07-1802
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2026-06-03 MST

Cite this

APA
Suehiro, Y., Wong, C.W., Chirieac, L.R., Kondo, Y., Shen, L., Webb, C.R., Chan, Y.W., Chan, A.S.Y., Chan, T.L., Wu, T., Rashid, A., Hamanaka, Y., Hinoda, Y., Shannon, R.L., Wang, X., Morris, J.S., Issa, J.J., Yuen, S.T., Leung, S.Y., &amp; Hamilton, S.R. (2008). Epigenetic-Genetic Interactions in the<i>APC/WNT, RAS/RAF</i>, and<i>P53</i>Pathways in Colorectal Carcinoma. <em>Clinical Cancer Research</em>. https://doi.org/10.1158/1078-0432.ccr-07-1802
Vancouver
Suehiro Y, Wong CW, Chirieac LR, Kondo Y, Shen L, Webb CR, et al. Epigenetic-Genetic Interactions in the<i>APC/WNT, RAS/RAF</i>, and<i>P53</i>Pathways in Colorectal Carcinoma. Clinical Cancer Research. 2008. doi:10.1158/1078-0432.ccr-07-1802.
BibTeX
@article{yutaka2008Epigen, title = {Epigenetic-Genetic Interactions in the<i>APC/WNT, RAS/RAF</i>, and<i>P53</i>Pathways in Colorectal Carcinoma}, author = {Yutaka Suehiro and Chi Wai Wong and Lucian R. Chirieac and Yutaka Kondo and Lanlan Shen and C. Renee Webb and Yee Wai Chan and Annie S Y Chan and Tsun Leung Chan and Tsung‐Teh Wu and Asif Rashid and Yuichiro Hamanaka and Yuji Hinoda and Rhonda L. Shannon and Xuemei Wang and Jeffrey S. Morris and Jean‐Pierre J. Issa and Siu Tsan Yuen and Suet Yi Leung and Stanley R. Hamilton}, journal = {Clinical Cancer Research}, year = {2008}, doi = {10.1158/1078-0432.ccr-07-1802}, }

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