The relationship between methionine synthase rs1805087 polymorphism and hematological cancers risk

Author:

Bai Yanliang12,Drokow Emmanuel Kwateng3ORCID,Waqas Ahmed Hafiz Abdul1,Song Juanjuan1,Akpabla Gloria Selorm4,Kumah Maame Awoyoe5,Agyekum Emmanuel Bamfo6,Neku Enyonam Adjoa6,Sun Kai12

Affiliation:

1. Department of Haematology, Zhengzhou University People's Hospital & Henan Provincial People's Hospital Henan, 450003, Zhengzhou, PR China

2. Department of Haematology, Henan University People's Hospital, School of Clinical Medicine, Henan University, Zhengzhou, 450003, Henan, PR China

3. Department of Radiation Oncology, Zhengzhou University People's Hospital & Henan Provincial People's Hospital Henan, 450003, Zhengzhou, PR China

4. Department of Internal Medicine, Tianjin Medical University, 300070, Tianjin, PR China

5. Department of Internal Medicine, University of Ghana Medical School, KB 77 Korle Bu-Accra, Ghana

6. School of Pharmacy, Zhengzhou University, 450001, Zhengzhou, Henan, PR China

Abstract

Background: The relationship between hematological cancer susceptibility and methionine synthase MTR A2756G (rs1805087) polymorphism is inconclusive based on data from past studies. Hence, this updated meta-analysis was conducted to investigate the relationship between methionine synthase reductase (MTR) rs1805087 polymorphism and hematological cancers. Method: We searched EMBASE, Google Scholar, Ovid and PubMed databases for possible relevant articles up to December 31, 2019. Results: The overall pooled outcome of our analysis showed lack of association between the risk of hematological malignancies and MTR A2756G polymorphism under the allele model (G vs A: odds ratio = 1.001, 95% CI: 0.944–1.061; p = 0.983), recessive model (GG vs GA + AA: odds ratio = 1.050, 95% CI: 0.942–1.170; p = 0.382). Conclusion: The findings in this study demonstrate a lack of relationship between hematological cancers and MTR A2756G.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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