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Erschienen in: Clinical and Translational Oncology 2/2014

01.02.2014 | Research Article

The adiponectin gene single-nucleotide polymorphism rs1501299 is associated with hepatocellular carcinoma risk

verfasst von: X. Cai, Y. Gan, Y. Fan, J. Hu, Y. Jin, F. Chen, T. Chen, Y. Sun, J. Wang, W. Qin, Hong Tu

Erschienen in: Clinical and Translational Oncology | Ausgabe 2/2014

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Abstract

Purpose

Increasing lines of evidence have suggested that adiponectin, an adipocyte-derived hormone, plays an important role in the development of hepatocellular carcinoma (HCC). However, the relationship between genetic variants of the adiponectin gene (ADIPOQ) and HCC has not been previously explored. Therefore, we performed a case–control study to examine the association of haplotype-tagging single-nucleotide polymorphisms (SNPs) in ADIPOQ with HCC risk.

Methods

Five haplotype-tagging SNPs of ADIPOQ (rs266729, rs822395, rs822396, rs2241766 and rs1501299) were genotyped in 200 HCC patients and 200 non-HCC controls by PCR amplification and direct sequencing. Logistic regression was used to estimate the risk of HCC associated with each individual SNP and we adjusted for multiple testing by the Bonferroni correction.

Results

Of the five tested SNPs, rs1501299 showed a strong and significant association with HCC risk even after the Bonferroni correction. After adjusting for the serological status of the hepatitis virus B core antibody and for other SNPs, the odds ratios were 4.33 [95 % confidence interval (CI) 2.07–9.05; corrected P < 0.005] and 3.71 (95 % CI 1.84–7.48; corrected P < 0.005) for the GG genotype and GG/GT combined genotype, respectively, versus the TT genotype.

Conclusions

This is the first report, demonstrating an association of ADIPOQ polymorphisms with HCC risk. Our results implicate the ADIPOQ SNP rs1501299 as a susceptibility locus for HCC.
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Metadaten
Titel
The adiponectin gene single-nucleotide polymorphism rs1501299 is associated with hepatocellular carcinoma risk
verfasst von
X. Cai
Y. Gan
Y. Fan
J. Hu
Y. Jin
F. Chen
T. Chen
Y. Sun
J. Wang
W. Qin
Hong Tu
Publikationsdatum
01.02.2014
Verlag
Springer Milan
Erschienen in
Clinical and Translational Oncology / Ausgabe 2/2014
Print ISSN: 1699-048X
Elektronische ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-013-1056-7

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