AS721 - Exploring MGMT constitutional methylation and the MGMT SNP rs16906252 as risk factors for cancer coli, glioblastomas and diffuse large B-cell lymphoma in the WHI study

Investigator Names and Contact Information

Per Lonning (per.lonning@helse-bergen.no)

Introduction/Intent

Here, we will confirm constitutional primary epimutations of MGMT to be a cancer risk factor by evaluating WBC MGMT methylation as risk factor for colorectal cancer, glioblastomas and high-grade lymphomas. Data generated will be used also to model the mechanism(s) of CpG methylation building up across the promotor area, evaluating the different models outlined in Figure 1.

Specific aims.

  1. We will assess the HR for right-sided and left-sided colon cancer separately related to WBC MGMT methylation status using a case-control designed study
  2. We will assess the HR for glioblastoma multiforme related to WBC MGMT methylation status using a case-control designed study
  3. We will assess the HR for high-grade diffuse B-cell lymphomas related to WBC MGMT methylation status using a case-control designed study

Related Papers

MGMT epimutations and risk of incident cancer of the colon, glioblastoma multiforme, and diffuse large B cell lymphomas

Oleskii Nikolaienko et al., 2025/2 PubMed #39980037 MSID: 5054
Background: Constitutional BRCA1 epimutations (promoter hypermethylation) are associated with an elevated risk of triple-negative breast cancer and high-grade serous ovarian cancer. While MGMT epimutations are frequent in colon cancer, glioblastoma, and B-cell lymphoma, it remains unknown whether constitutional MGMT epimutations are associated with risk of any of these malignancies. Methods: We designed a nested case-control study, assessing potential associations between MGMT epimutations in bl...
Keywords: Colon Cancer; Glioblastoma Multiforme; Large B-Cell Lymphomas; Mgmt Promoter; Epimutations; Hypermethylation
Related Studies: 721