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Contribution of Inflammatory Cytokine Interleukin-18 Genotypes to Renal Cell Carcinoma

Authors :
Chia-Wen Tsai
Wei-Lan Yeh
Da Tian Bau
Wen-Shin Chang
Chien Chih Yu
Hui-Yi Lin
Te Chun Shen
Hsi Chin Wu
Source :
International Journal of Molecular Sciences, Volume 20, Issue 7, International Journal of Molecular Sciences, Vol 20, Iss 7, p 1563 (2019)
Publication Year :
2019
Publisher :
Multidisciplinary Digital Publishing Institute, 2019.

Abstract

Interleukin-18 (IL-18) is a multi-functional immuno-mediator in the development and progression of many types of infectious and inflammatory diseases. In this study, we evaluated the contribution of IL-18 genotypes to renal cell carcinoma (RCC) in Taiwan via the genotyping of IL-18 -656 (A/C), -607 (A/C), and -137 (G/C). Moreover, we analyzed their interactions with smoking, alcohol drinking, hypertension, and diabetes status. The results showed an association of the AC and CC genotypes of IL-18 &minus<br />607 with a significant decrease in the risk of RCC compared with the AA genotype (odds ratio (OR) = 0.44 and 0.35, 95% confidence interval (CI) = 0.27&ndash<br />0.72 and 0.18&ndash<br />0.66, p = 0.0008 and 0.0010, respectively). Furthermore, a significantly lower frequency of the C allele at -607 was observed in the RCC group (35.3% vs. 49.8%<br />OR = 0.53<br />95% CI = 0.35&ndash<br />0.71, p = 0.0003). However, IL-18 -656 and -137 did not exhibit a likewise differential distribution of these genotypes between the control and case groups. Stratifying the population according to smoking, alcohol drinking, hypertension, and diabetes status revealed a different distribution of IL-18 -607 genotypes among non-smokers, non-drinkers, and patients without diabetes, but not among smokers, drinkers, or patients with diabetes. These findings suggest that IL-18 -607 genotypes may play a role in the etiology and progression of RCC in Taiwan and may serve as a useful biomarker for early detection.

Details

Language :
English
ISSN :
14220067
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....27c8f92fe741e2f9fe603ef65980ac60
Full Text :
https://doi.org/10.3390/ijms20071563