Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Mar 4;59(1):9.
doi: 10.1007/s44313-024-00007-9.

Impact of CYP1A1 variants on the risk of acute lymphoblastic leukemia: evidence from an updated meta-analysis

Affiliations

Impact of CYP1A1 variants on the risk of acute lymphoblastic leukemia: evidence from an updated meta-analysis

Imen Frikha et al. Blood Res. .

Abstract

Objective: Our study aimed to investigate the association between cytochrome P450 1A1 (CYP1A1) polymorphisms (T3801C and A2455G) and acute lymphoblastic leukemia (ALL) risk, considering genetic models and ethnicity.

Materials and methods: PubMed, Embase, Web of Knowledge, Scopus, and the Cochrane electronic databases were searched using combinations of keywords related to CYP1A1 polymorphisms and the risk of ALL. Studies retrieved from the database searches underwent screening based on strict inclusion and exclusion criteria.

Results: In total, 2822 cases and 4252 controls, as well as 1636 cases and 2674 controls of the C3801T and A2455G variants of CYP1A1, respectively, were included in this meta-analysis. The T3801C polymorphism of CYP1A1 significantly increases the risk of ALL, particularly those observed in Asian and Hispanic populations, independent of age. Similarly, the A2455G polymorphism of CYP1A1 plays a significant role in the susceptibility to ALL in all genetic models, except the heterozygous form. This association was observed mainly in mixed populations and in both children and adults (except in the heterozygous model).

Conclusion: Our comprehensive analysis indicates that the T3801 and A2455G polymorphisms of CYP1A1 may increase the risk of ALL depending on ethnicity. Therefore, both variants should be considered promising biomarkers for ALL risk. Further large-scale investigations are necessary to assess other factors, such as gene-gene or gene-environment interactions.

Keywords: Acute lymphoblastic leukemia; Cytochrome; Meta-analysis; Risk.

PubMed Disclaimer

Conflict of interest statement

None.

Figures

Fig. 1
Fig. 1
Flow diagram for article identification and exclusion
Fig. 2
Fig. 2
Forest plot of C3801T Polymorphism and ALL Risk under Different Models (A-E)
Fig. 3
Fig. 3
Forest plot of A2455G Polymorphism and ALL Risk under Different Models (A-E)

Similar articles

References

    1. Terwilliger T, Abdul-Hay M. Acute lymphoblastic leukemia: a comprehensive review and 2017 update. Blood Cancer J. 2017;7:e577. doi: 10.1038/bcj.2017.53. - DOI - PMC - PubMed
    1. Chokkalingam AP, Buffler PA. Genetic susceptibility to childhood leukaemia. Radiat Prot Dosim. 2008;132:119–129. doi: 10.1093/rpd/ncn255. - DOI - PMC - PubMed
    1. Severson RK, Ross JA. The causes of acute leukemia. Curr Opin Oncol. 1999;11:20–24. doi: 10.1097/00001622-199901000-00005. - DOI - PubMed
    1. Rendic S, Guengerich FP. Contributions of human enzymes in carcinogen metabolism. Chem Res Toxicol. 2012;25:1316–1383. doi: 10.1021/tx300132k. - DOI - PMC - PubMed
    1. Samuel W, Lovell J, Christine C, Kathi H, editors. Cancer and the Environment: Gene-Environment Interactions. Washington, D.C.: National Academies Press; 2002. 10.17226/10464.

LinkOut - more resources