Literature DB >> 25716203

Clinicopathological significance and potential drug target of O6-methylguanine-DNA methyltransferase in colorectal cancer: a meta-analysis.

Chen-Guo Zheng1, Chun Jin, Le-Chi Ye, Nian-Zhao Chen, Zong-Jing Chen.   

Abstract

Emerging evidence indicates that O(6)-methylguanine-DNA methyltransferase (MGMT) is a candidate for tumor suppression in several types of human tumors including colorectal cancer (CRC). However, the correlation between MGMT hypermethylation and clinicopathological characteristics of CRC remains unclear. In this study, we conducted a systematic review and meta-analysis to quantitatively evaluate the effects of MGMT hypermethylation on the incidence of CRC and clinicopathological characteristics. A comprehensive literature search was done from Web of Science, the Cochrane Library Database, PubMed, EMBASE, CINAHL, and the Chinese Biomedical Database for related research publications written in English and Chinese. Methodological quality of the studies was also evaluated. Analyses of pooled data were performed with Review Manager 5.2. Odds ratio (OR) and hazard ratio (HR) were calculated and summarized, respectively. Final analysis from 28 eligible studies was performed. MGMT hypermethylation is found to be significantly higher in CRC than in normal colorectal mucosa, the pooled OR from 13 studies including 1085 CRC and 899 normal colorectal mucosa, OR = 6.04, 95 % confidence interval (CI) = 4.69-7.77, p < 0.00001. MGMT hypermethylation is also significantly higher in colorectal adenoma than in normal colorectal mucosa, but it is significantly less compared to that in CRC patients. Interestingly, MGMT hypermethylation is correlated with sex status and is significantly higher in female than in male. MGMT hypermethylation is also associated with high levels of microsatellite instability (MSI). The pooled HR for overall survival (OS) shows that MGMT hypermethylation is not associated with worse survival in CRC patients. The results of this meta-analysis suggest that MGMT hypermethylation is associated with an increased risk and high levels of MSI and may play an important role in CRC initiation. However, MGMT hypermethylation may play an important role in the early stage of CRC progression and development, as well as having limited value in prediction of prognosis in CRC patients. We also discussed that MGMT may serve as a potential drug target of CRC.

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Year:  2015        PMID: 25716203     DOI: 10.1007/s13277-015-3254-0

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  51 in total

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Authors:  T Ishii; J Murakami; K Notohara; H M Cullings; H Sasamoto; T Kambara; Y Shirakawa; Y Naomoto; M Ouchida; K Shimizu; N Tanaka; J R Jass; N Matsubara
Journal:  Gut       Date:  2006-06-19       Impact factor: 23.059

2.  Hypermethylation of CpG island in O6-methylguanine-DNA methyltransferase gene was associated with K-ras G to A mutation in colorectal tumor.

Authors:  Jian Qi; You-Qing Zhu; Mei-Fang Huang; Dong Yang
Journal:  World J Gastroenterol       Date:  2005-04-07       Impact factor: 5.742

3.  Prognostic significance of O6-methylguanine-DNA methyltransferase determined by promoter hypermethylation and immunohistochemical expression in anaplastic gliomas.

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Journal:  Clin Cancer Res       Date:  2005-07-15       Impact factor: 12.531

4.  Evaluation of methylation of MGMT (O⁶-methylguanine-DNA methyltransferase) gene promoter in sporadic colorectal cancer.

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Review 5.  DNA methylation data analysis and its application to cancer research.

Authors:  Xiaotu Ma; Yi-Wei Wang; Michael Q Zhang; Adi F Gazdar
Journal:  Epigenomics       Date:  2013-06       Impact factor: 4.778

6.  Methylation pattern of the O6-methylguanine-DNA methyltransferase gene in colon during progressive colorectal tumorigenesis.

Authors:  Takeshi Nagasaka; Ajay Goel; Kenji Notohara; Takaomi Takahata; Hiromi Sasamoto; Takuyuki Uchida; Naoshi Nishida; Noriaki Tanaka; Clement Richard Boland; Nagahide Matsubara
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Review 7.  Correlation of O6-methylguanine methyltransferase (MGMT) promoter methylation with clinical outcomes in glioblastoma and clinical strategies to modulate MGMT activity.

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Review 8.  DNA methylation pattern as important epigenetic criterion in cancer.

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Journal:  Genet Res Int       Date:  2013-12-23

9.  Correlation of MLH1 and MGMT methylation levels between peripheral blood leukocytes and colorectal tissue DNA samples in colorectal cancer patients.

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Journal:  Oncol Lett       Date:  2013-08-23       Impact factor: 2.967

10.  DNA methylation of the p14ARF, RASSF1A and APC1A genes as an independent prognostic factor in colorectal cancer patients.

Authors:  Torbjörn K Nilsson; Zarah M Löf-Öhlin; Xiao-Feng Sun
Journal:  Int J Oncol       Date:  2012-10-30       Impact factor: 5.650

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  4 in total

Review 1.  Biomarkers for immune therapy in colorectal cancer: mismatch-repair deficiency and others.

Authors:  Manojkumar Bupathi; Christina Wu
Journal:  J Gastrointest Oncol       Date:  2016-10

Review 2.  High microsatellite instability (MSI-H) colorectal carcinoma: a brief review of predictive biomarkers in the era of personalized medicine.

Authors:  Zoran Gatalica; Semir Vranic; Joanne Xiu; Jeffrey Swensen; Sandeep Reddy
Journal:  Fam Cancer       Date:  2016-07       Impact factor: 2.375

3.  DNA methylation assay for colorectal carcinoma.

Authors:  Ji-Jun Chen; Ai-Qin Wang; Qing-Qi Chen
Journal:  Cancer Biol Med       Date:  2017-02       Impact factor: 4.248

4.  Sex-specific clinicopathological significance of novel (Frizzled-7) and established (MGMT, IDH1) biomarkers in glioblastoma.

Authors:  Salveena Schiffgens; Ludwig Wilkens; Alba A Brandes; Tatiana Meier; Enrico Franceschi; Mario Ermani; Christian Hartmann; Ibrahim Erol Sandalcioglu; Claudia A Dumitru
Journal:  Oncotarget       Date:  2016-08-23
  4 in total

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