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. 2012 Dec 22;4(1):71–81. doi: 10.1007/s13238-012-2067-9

Combined effects of p53 and MDM2 polymorphisms on susceptibility and surgical prognosis in hepatitis B virus-related hepatocellular carcinoma

Yun Yang 1, Tian Xia 2, Ning Li 3, Jin Zhang 1, Yuan Yang 1, Wenming Cong 4, Qiang Deng 2, Ke Lan 2,, Weiping Zhou 1,
PMCID: PMC4875440  PMID: 23292895

Abstract

The p53 signaling pathway works as a potent barrier to tumor progression. Two single nucleotide polymorphisms (SNPs) in the gene loci of p53 pathway, p53 codon 72 Arg72Pro and MDM2 SNP309 (T > G), have been shown to cause perturbation of p53 function, but the effect of the two SNPs on the risk of hepatocellular carcinoma (HCC) remains inconsistent. This study investigated the influence of combined p53 Arg72Pro and MDM2 SNP309 on the risk of developing HCC in patients with chronic hepatitis B virus infection, and evaluated the significance of the two combined SNPs on patient prognosis. In total, 350 HCC patients, 230 non-HCC patients, and 96 healthy controls were genotyped for the p53 Arg72Pro and MDM2 SNP309. The combined p53 Pro/Pro and MDM2 G/G genotype was significantly associated with HCC risk (P = 0.047). Multivariate analysis indicated that combined p53 Pro/Pro and MDM2 G/G genotype was an independent factor affecting recurrence and survival (P < 0.05). Patients with combined p53 Pro/Pro and MDM2 G/G genotypes had a poorer prognosis than other genotypes, P < 0.01 for both disease-free survival (DFS) and overall survival (OS). DFS and OS rates also differed significantly between Barcelona Clinic Liver Cancer (BCLC) stage A patients with combined p53 Pro/Pro and MDM2 G/G and other genotypes (P < 0.05). Thus, the combined p53 Pro/Pro and MDM2 G/G genotype is associated with increased risk of developing HCC and is an independent adverse prognostic indicator in early stage HCC.

Electronic Supplementary Material

Supplementary material is available for this article at 10.1007/s13238-012-2067-9 and is accessible for authorized users.

Keywords: hepatocellular carcinoma, p53, MDM2, single nucleotide polymorphisms, prognosis

Electronic supplementary material

13238_2012_2067_MOESM1_ESM.pdf (175.9KB, pdf)

Supplementary material, approximately 175 KB.

Footnotes

These authors contributed equally to the work.

Electronic Supplementary Material

Supplementary material is available for this article at 10.1007/s13238-012-2067-9 and is accessible for authorized users.

Contributor Information

Ke Lan, Email: lanke@sibs.ac.cn.

Weiping Zhou, Email: ehphwp@126.com.

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Supplementary Materials

13238_2012_2067_MOESM1_ESM.pdf (175.9KB, pdf)

Supplementary material, approximately 175 KB.


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