Impacts of Interleukin-10 Promoter Genotypes on Prostate Cancer

Author:

Chin Yu-Ting12,Tsai Chung-Lin3,Ma Hung-Huan4,Cheng Da-Chuan5ORCID,Tsai Chia-Wen126,Wang Yun-Chi12,Shih Hou-Yu12,Chang Shu-Yu127,Gu Jian6ORCID,Chang Wen-Shin126,Bau Da-Tian1268ORCID

Affiliation:

1. Graduate Institute of Biomedical Sciences, China Medical University, Taichung 404333, Taiwan

2. Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung 404327, Taiwan

3. Division of Cardiac and Vascular Surgery, Cardiovascular Center, Taichung Veterans General Hospital, Taichung 407219, Taiwan

4. Division of Nephrology, Department of Internal Medicine, Taichung Tzu Chi Hospital, Taichung 427003, Taiwan

5. Department of Biomedical Imaging and Radiological Science, China Medical University, Taichung 404333, Taiwan

6. Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

7. Department of Nephrology, Chang-Hua Hospital, Ministry of Health and Welfare, Changhua 51341, Taiwan

8. Department of Bioinformatics and Medical Engineering, Asia University, Taichung 413305, Taiwan

Abstract

Prostate cancer (PCa) is a multifactorial disease influenced by genetic, environmental, and immunological factors. Genetic polymorphisms in the interleukin-10 (IL-10) gene have been implicated in PCa susceptibility, development, and progression. This study aims to assess the contributions of three IL-10 promoter single nucleotide polymorphisms (SNPs), A-1082G (rs1800896), T-819C (rs3021097), and A-592C (rs1800872), to the risk of PCa in Taiwan. The three IL-10 genotypes were determined using PCR-RFLP methodology and were evaluated for their contributions to PCa risk among 218 PCa patients and 436 non-PCa controls. None of the three IL-10 SNPs were significantly associated with the risks of PCa (p all > 0.05) in the overall analyses. However, the GG at rs1800896 combined with smoking behavior was found to significantly increase the risk of PCa by 3.90-fold (95% confidence interval [95% CI] = 1.28–11.89, p = 0.0231). In addition, the rs1800896 AG and GGs were found to be correlated with the late stages of PCa (odds ratio [OR] = 1.90 and 6.42, 95% CI = 1.05–3.45 and 2.30–17.89, p = 0.0452 and 0.0003, respectively). The IL-10 promoter SNP, A-1082G (rs1800896), might be a risk factor for PCa development among smokers and those at late stages of the disease. These findings should be validated in larger and more diverse populations.

Funder

Taichung Veterans General Hospital

Taichung Tzu Chi Hospital

Publisher

MDPI AG

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