Analysis of MMP-2-735C/T (rs2285053) and MMP-9-1562C/T (rs3918242) Polymorphisms in the Risk Assessment of Developing Lung Cancer

被引:7
作者
Wadowska, Katarzyna [1 ]
Blasiak, Piotr [2 ,3 ]
Rzechonek, Adam [3 ]
Sliwinska-Mosson, Mariola [1 ]
机构
[1] Wroclaw Med Univ, Dept Med Lab Diagnost, Div Clin Chem & Lab Haematol, Borowska 211A, PL-50556 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept & Clin Thorac Surg, Grabiszynska 105, PL-53439 Wroclaw, Poland
[3] Lower Silesian Ctr Oncol Lung Dis & Haematol, Dept Thorac Surg, Grabiszynska 105, PL-53439 Wroclaw, Poland
关键词
lung cancer; polymorphism; matrix metalloproteinases; MMP-2-735C; T; rs2285053; MMP-9-1562C; rs3918242; ethnicity; GENE POLYMORPHISMS; MOLECULAR EPIDEMIOLOGY; MMP-2; POLYMORPHISMS; CIGARETTE-SMOKING; ASSOCIATION; METALLOPROTEINASE-2; SUSCEPTIBILITY; PROMOTER; METASTASIS; EXPRESSION;
D O I
10.3390/ijms241310576
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinase (MMP)-2 and -9 are gelatinases which are capable of degrading type IV collagen and have been linked to cancer invasion and metastatic development. MMP-2 and MMP-9 gene polymorphisms may affect their biological function, and thus their role in cancer development and progression. We analyzed the association of the polymorphism frequencies of MMP-2-735C/T and MMP-9-1562C/T with MMP-2 and MMP-9 serum concentrations, as well as their potential effects in lung cancer patients. We conducted a retrospective, case-control study consisting of 112 lung cancer patients and 100 healthy individuals from a Caucasian population in Poland. Polymerase chain reaction with restriction fragment length polymorphism (PCR/RFLP) and electrophoresis was used to genotype genomic DNA from whole blood samples. MMP-2 and MMP-9 serum concentrations were then determined using ELISA. For statistical analysis, Statistica version 13 from TIBCO Software Inc. was utilized with a significance level MMP-2-735CC (OR = 5.39; 95% CI = 0.62-47.17; p = 0.238504) and -735CT genotype (OR = 7.22; 95% CI = 0.78-67.14; p = 0.072836), as well as MMP-9-1562CC (OR = 1.45; 95% CI = 0.31-6.70; p = 0.757914) and -1562CT genotype (OR = 1.60; 95% CI = 0.33-7.83; p = 0.548801) were associated with a higher risk of lung cancer. There were statistically significant differences observed in the MMP-2 concentration between individuals with the -735CC genotype and the -735CT genotype (non-smoking control: 204.04 ng/mL vs. 237.00 ng/mL, respectively, p = 0.041479; adenocarcinoma patients: 157.69 ng/mL vs. 126.37 ng/mL, respectively, p = 0.013222), as well as differences in the MMP-9 concentration between individuals with the -1562CC genotype and the -1562CT genotype (smoking control: 385.67 ng/mL vs. 562.80 ng/mL, respectively, p = 0.000936; patients with other lung neoplasms: 821.64 ng/mL vs. 928.88 ng/mL, respectively p = 0.023315). The role of MMP-2-735C/T and MMP-9 -1562C/T polymorphisms in an increased risk of lung cancer cannot be dismissed. Specific genotypes affect MMP-2 and MMP-9 concentrations in both lung cancer patients and healthy controls, which may thereby increase lung cancer risk, disease aggressiveness, and patient survival outcomes.
引用
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页数:20
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