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Published on: June 21, 2018
Contribution of Matrix Metalloproteinase-9 rs3918242 Genotypes to Childhood Leukemia Risk
Chien-Chung Kuo1, Chia-Wen Tsai2,3, Wen-Shin Chang2,3
1Department of Pediatric Orthopedics, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Background/Aim:
A single study has shown positive association and genotype-phenotype correlation between metalloproteinase-9 (MMP-9) promoter genotypes and adult acute lymphocytic leukemia (ALL). However, there is no report about childhood ALL. Thus, this study aimed at examining the role of MMP-9 rs3918242 genotypes in childhood ALL risk.
Patients And Methods:
A total of 266 childhood ALL cases and 266 healthy controls in Taiwan were examined for their MMP-9 rs3918242 genotypes via polymerase chain reaction-restriction fragment length polymorphism methodology.
Results:
The MMP-9 rs3918242 CT or TT genotype carriers only had a slightly increased risk compared with CC carriers (p=0.6386 and 0.6005, respectively). The allelic frequency analysis also supported the idea that the variant T allele at MMP-9 rs3918242 is not differentially distributed between the case and control groups (p=0.4834).
Conclusion:
MMP-9 rs3918242 genotypes may indirectly influence the risk of childhood ALL. Further validations in other populations and analysis of the detail mechanisms are needed.
Insights
Metalloproteinase-9 (MMP-9) rs3918242 genotypes do not significantly increase childhood acute lymphocytic leukemia (ALL) risk. Further research is needed to explore potential indirect influences and underlying mechanisms in diverse populations.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Previous research indicated a link between metalloproteinase-9 (MMP-9) promoter genotypes and adult acute lymphocytic leukemia (ALL).
- No studies have investigated this association in the context of childhood ALL.
- The MMP-9 gene plays a role in various biological processes, including inflammation and tissue remodeling, which could be relevant to cancer development.
Purpose of the Study:
- To investigate the association between the MMP-9 rs3918242 polymorphism and the risk of childhood ALL.
- To determine if specific MMP-9 genotypes are correlated with an increased susceptibility to childhood ALL in a Taiwanese population.
Main Methods:
- A case-control study was conducted involving 266 children diagnosed with ALL and 266 age- and sex-matched healthy controls from Taiwan.
- Genotyping of the MMP-9 rs3918242 polymorphism was performed using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method.
Main Results:
- No statistically significant difference in the frequency of MMP-9 rs3918242 genotypes (CT or TT vs. CC) was observed between childhood ALL cases and healthy controls.
- Allelic frequency analysis revealed that the variant T allele of MMP-9 rs3918242 was not differentially distributed between the case and control groups.
- The study found no significant association between MMP-9 rs3918242 genotypes and the risk of developing childhood ALL.
Conclusions:
- The MMP-9 rs3918242 genotypes do not appear to be a significant risk factor for childhood ALL in the studied Taiwanese population.
- While direct association was not found, the study suggests that MMP-9 genotypes might indirectly influence childhood ALL risk through complex mechanisms.
- Further large-scale validation studies in diverse ethnic groups and detailed mechanistic investigations are warranted to fully elucidate the role of MMP-9 in childhood ALL.
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