NFKB1 -94 insertion/deletion polymorphism and cancer risk: a meta-analysis
Linlin Xu1, Shaoyi Huang, Wei Chen
1Department of Clinical Laboratory, The First People's Hospital of Yancheng, Yancheng, Jiangsu, 224001, China, xulinlin1212@126.com.
Summary
The NFKB1 -94 insertion/deletion polymorphism is linked to increased cancer risk, particularly in Asian populations. This genetic variation may influence susceptibility to certain cancers, warranting further investigation.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Conflicting results exist regarding the association between the NFKB1 -94 insertion/deletion polymorphism and cancer risk.
- The NFKB1 gene plays a crucial role in inflammatory and immune responses, potentially influencing cancer development.
Purpose of the Study:
- To conduct a comprehensive meta-analysis defining the effect of the NFKB1 -94 insertion/deletion polymorphism on overall cancer risk.
- To investigate ethnic and cancer-type specific associations with this polymorphism.
Main Methods:
- A systematic literature search was performed using PubMed to identify relevant studies.
- Twenty-three studies, including 6,494 cancer cases and 9,884 controls, were meta-analyzed under various genetic models.
Main Results:
- A significant overall association was observed between the NFKB1 -94 insertion/deletion polymorphism and cancer risk across all genetic models.
- Subgroup analyses revealed significant associations in the Asian population but not in the Caucasian population.
- Specific cancer types like oral cancer (OC), hepatocellular carcinoma (HCC), and oral squamous cell carcinoma (OSCC) showed significant associations, unlike breast cancer (BC) and lung cancer (LC).
Conclusions:
- The NFKB1 -94 insertion/deletion polymorphism is associated with cancer risk, with a notable impact observed in the Asian population.
- This genetic polymorphism may contribute to cancer susceptibility, particularly in specific ethnic groups and cancer types.
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