Genetic variants of interleukin‐1RN and interleukin‐1β genes and risk of cervical cancer
2008
Objectives Inflammation plays a major role in pathogenesis of cervical cancer. We planned to study whether polymorphisms in inflammation-related genes, IL-1RN (VNTR) and IL-1β (-511C/T), are associated with risk of cervical cancer.
Design Case–control study.
Setting Uttar Pradesh state in India.
Sample One hundred and fifty, histopathologically confirmed cases with cervical cancer and 162 age-, ethnicity-matched, cervical cytology negative, healthy controls were recruited to this study.
Methods Genotyping of IL-1RN (VNTR) and IL-1β (-511C/T) polymorphisms was performed using polymerase chain reaction (PCR)/PCR–restriction fragment length polymorphism. Power of study was 80% with type 1 error of 0.05. Haplotypes frequencies were obtained by computer package ‘Arlequin’.
Main outcome measures Haplotype IL-1RN*2/IL-1β*T is associated with higher risk and of cervical cancer.
Results IL-1RN genotypes 1/2 and 2/2 were associated with significantly elevated risk of cervical cancer (OR = 3.3; P= 4.9 × 10−6 and OR = 2.9, P= 0.02). Similarly, TT genotype of IL-1βpolymorphism was significantly higher in cases compared with controls (57.7 versus 38.3%; OR = 2.8; P = 0.012). 2/2 genotype of IL-1RN (OR = 4.8, P = 0.0006) and TT genotype of IL-1β(OR = 5.2; P = 0.02) were associated with the higher stages (III) of cervical cancer. Haplotypes 1T (IL-1RN*1/IL-1β*T) and 2T (IL-1RN*2/IL-1β*T) were also significantly associated with higher susceptibility to cervical cancer and its progression. Logistic regression analysis suggests IL-1RN allele 2 and IL-1β-511T were independently associated with increased risk for cervical cancer.
Conclusion IL-1RN*2 and IL-1β -511*T in various combinations of genotypes and haplotypes are associated with higher susceptibility for cervical cancer.
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