What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?
- PMID: 34637096
- PMCID: PMC8505470
- DOI: 10.1007/s11033-021-06813-z
What are the roles of global DNA and APC 2 gene promotor hypermethylation in multiple myeloma?
Abstract
Background: In today's practice, gene-based approaches come to the fore in the determination of prognosis and treatment preferences of multiple myeloma (MM). DNA methylation is one of the new approach parameters. DNA methylation occurs by the addition of a methyl group to cytosines in CpG dinucleotides. In this study, besides comparing the global DNA and APC 2 gene promotor hypermethylation between our patients with MM and healthy control group, we aimed to demonstrate the effect of hypermethylation on MM treatment responses and survival.
Methods and results: 38 patients diagnosed with MM between January 2016 and January 2020 and 50 healthy controls were included in the study. The initial hypermethylation of the patients and the healthy control group were statistically analyzed. In addition, the increase in hypermethylation in the MM group before and after the first series of treatments were analyzed within themselves. There is a significant difference between the patients with MM diagnosis and the healthy control group in terms of the initial global hypermethylation (P = 0.001). In patients with MM, hypermethylation was significantly higher. Global hypermethylation in the post-treatment measurements was significantly increased in comparison to the pre-treatment state (P = 0.012). In terms of APC 2 promotor gene-specific hypermethylation, no significant differences were detected between pre- and post-treatment values (P = 0.368).
Conclusions: This study represents valuable data with the initial global DNA hypermethylation results in the MM patient group and the increase in hypermethylation post-treatment. it will shed light on future studies.
Keywords: DNA methylation; Multiple myeloma; Response; Survival; Treatment.
© 2021. The Author(s), under exclusive licence to Springer Nature B.V.
Conflict of interest statement
None to declare.
Similar articles
-
Qualitative analysis of Adenomatous Polyposis Coli promoter: hypermethylation, engagement and effects on survival of patients with esophageal cancer in a high risk region of the world, a potential molecular marker.BMC Cancer. 2009 Jan 17;9:24. doi: 10.1186/1471-2407-9-24. BMC Cancer. 2009. PMID: 19149902 Free PMC article.
-
Epigenetic silencing of LPP/miR-28 in multiple myeloma.J Clin Pathol. 2018 Mar;71(3):253-258. doi: 10.1136/jclinpath-2017-204501. Epub 2017 Aug 3. J Clin Pathol. 2018. PMID: 28775176 Free PMC article.
-
Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers.Genome Res. 2015 Apr;25(4):478-87. doi: 10.1101/gr.180240.114. Epub 2015 Feb 2. Genome Res. 2015. PMID: 25644835 Free PMC article.
-
An integrated epigenomic-transcriptomic landscape of lung cancer reveals novel methylation driver genes of diagnostic and therapeutic relevance.Theranostics. 2021 Mar 11;11(11):5346-5364. doi: 10.7150/thno.58385. eCollection 2021. Theranostics. 2021. PMID: 33859751 Free PMC article.
-
APC hypermethylation for early diagnosis of colorectal cancer: a meta-analysis and literature review.Oncotarget. 2017 Jul 11;8(28):46468-46479. doi: 10.18632/oncotarget.17576. Oncotarget. 2017. PMID: 28515349 Free PMC article. Review.
Cited by
-
Genetic, epigenetic, and molecular determinants of multiple myeloma and precursor plasma cell disorders: a pathophysiological overview.Med Oncol. 2025 Jun 3;42(7):234. doi: 10.1007/s12032-025-02807-0. Med Oncol. 2025. PMID: 40459694 Review.
-
Epigenetic and genetic investigation of SOCS-1 gene in patients with multiple myeloma.Blood Res. 2022 Dec 31;57(4):250-255. doi: 10.5045/br.2022.2022097. Epub 2022 Oct 27. Blood Res. 2022. PMID: 36289192 Free PMC article.
References
-
- Hillengass J, Usmani S, Rajkumar SV, et al. International myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders [published correction appears in Lancet Oncol. 2019 Jul;20(7):e346] Lancet Oncol. 2019;20(6):302–312. doi: 10.1016/S1470-2045(19)30309-2. - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases