Correction
13 Apr 2015: The PLOS ONE Staff (2015) Correction: Impact of TP53 Codon 72 and MDM2 SNP 309 Polymorphisms in Pancreatic Ductal Adenocarcinoma. PLOS ONE 10(4): e0126295. https://doi.org/10.1371/journal.pone.0126295 View correction
Figures
Abstract
Single-nucleotide polymorphisms (SNPs) of TP53 (codon 72, rs1042522) and MDM2 promoter (SNP 309, rs2279744) have been associated with risk for various human cancers. However, studies analyzing these polymorphisms in pancreatic ductal adenocarcinoma (PDAC) are lacking. We investigated TP53 codon 72 and MDM2 SNP 309 polymorphisms in 32 patients with PDAC, 16 patients with chronic pancreatitis (CP), and 32 normal controls, using formalin-fixed paraffin-embedded tissue. We also examined TP53 and MDM2 protein immunohistochemistry (IHC) to assess the involvement of these differences in malignant transformation and disease progression. TP53 Pro/Pro genotype was significantly more frequent in PDAC patients than in controls (65.6 vs. 15.6%, p < 0.001) and no significant difference was found between CP patients (37.5%) and controls. In MDM2 SNP 309, there were no significant differences among the three groups. Based on the Kaplan-Meier analysis, overall survival was significantly shorter in MDM2 G/G genotypes compared with other genotypes (G/T and T/T) (359 vs. 911 days, p = 0.016) whereas no significant differences in TP53 genotypes were observed (638 vs. 752 days, p = 0.471). Although TP53 IHC was frequent in PDAC patients (53.1%), TP53 and MDM2 protein expression was not correlated with polymorphisms. Our study demonstrated TP53 codon 72 polymorphism is potentially a genetic predisposing factor while MDM2 SNP 309 polymorphism might be useful in predicting survival outcome.
Citation: Hori Y, Miyabe K, Yoshida M, Nakazawa T, Hayashi K, Naitoh I, et al. (2015) Impact of TP53 Codon 72 and MDM2 SNP 309 Polymorphisms in Pancreatic Ductal Adenocarcinoma. PLoS ONE 10(3): e0118829. https://doi.org/10.1371/journal.pone.0118829
Academic Editor: Klaus Roemer, University of Saarland Medical School, GERMANY
Received: September 24, 2014; Accepted: December 2, 2014; Published: March 3, 2015
Copyright: © 2015 Hori et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This study was supported by a research grant from Aichi Cancer Research Foundation (http://www.acrf.or.jp/, no grant number) and the internal source of Nagoya City University Graduate School of Medical Sciences. The funders had no rule in study design, data collection and analysis, employment of any individuals, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Pancreatic ductal adenocarcinoma (PDAC) is a gastrointestinal neoplasm with high malignancy and poor prognosis. Incidence of PDAC has increased in recent years, but the therapeutic efficacy remains unsatisfactory. Complete surgical resection is an essential part of curative therapy. However, most tumors are unresectable and are treated primarily with chemotherapy and/or radiation [1–3]. Recent research has shown that single nucleotide polymorphisms (SNPs) of genes involved in the cell cycle play an important role in carcinogenesis [4–7] and that common polymorphisms may lead to altered susceptibility to PDAC and affect clinical outcome [7].
The tumor protein p53 (TP53) tumor suppressor pathway plays a critical role in cell cycle regulation and apoptosis in many cancers, including PDAC. A common polymorphism located in exon 4 of TP53 gene, resulting in a non-conservative arginine (Arg) to a proline (Pro) change at codon 72, is important for growth suppression and apoptotic function [8]. Additionally, the T to G allelic change introduced by mouse double minute 2 (MDM2) promoter SNP 309 was predicted to increase the affinity of the Sp1 transcription factor by extending the length of a Sp1 binding site, resulting in repressed tumor suppressor activity of the p53 pathway [4]. This finding was subsequently validated through in vitro DNA-protein binding and reporter plasmid cell-based assays [4]. These polymorphisms were investigated previously in peripheral blood samples from PDAC patients [9–11]. To our knowledge, in PDAC, no study has examined TP53 codon 72 and only one study has examined the MDM2 SNP 309 [12] polymorphism using formalin-fixed paraffin-embedded (FFPE) specimens. Furthermore, the relationship between these polymorphisms and malignant transformation has not been investigated in chronic pancreatitis (CP), which is considered a precancerous change.
Immunohistochemistry (IHC) is a method widely used for investigation of TP53 protein expression [13]. TP53 nuclear accumulation is considered a result of TP53 stabilization either by a mutation or cellular stresses. MDM2 is a downstream gene and its expression is induced by wild-type TP53. However, the expression of MDM2 protein can also occur independently of TP53, even if its stress induction is TP53-dependent. Therefore, IHC of MDM2 was suggested as a possible method to discriminate between functional and nonfunctional TP53 in human tumors [14].
In the present study, using IHC we examined the TP53 codon 72 and MDM2 SNP 309 polymorphisms and TP53 and MDM2 proteins in PDAC and CP patients to assess the involvement of these differences in the malignant transformation and disease progression.
Materials and Methods
Study population and samples
Between January 1997 and December 2010, PDAC patients and CP patients were retrospectively evaluated. We also cases of pancreatic epithelium from resected specimens without pancreatic disease as controls (normal controls). All cases were obtained from the archives of the Department of Pathology, Nagoya City University Graduate School of Medical Sciences and affiliated hospitals. The CP cases consisted of both alcoholic and idiopathic CP and were diagnosed based on the Zurich classification [15] including history of excessive alcohol intake (in excess of 80 g ethanol per day), calcification in the pancreas, or moderate to marked ductal lesions described in the Cambridge classification [16]. CP pathology was characterized by perilobular fibrosis and acinar destruction with acute and chronic inflammatory cells.
In order to determine the sample size, we conducted an interim analysis of TP53 IHC in 32 cases of PDAC and 21 normal controls. TP53 IHC was positive in 17 of the 32 PDAC patients (53.1%) and 3 of 21 normal controls (14.3%). For a 5% type I error with 80% statistical power, the required number of patients in each group was estimated to be 28. Therefore, additional normal controls gave 32 normal controls. All of the available CP cases were collected (n = 16).
This study was approved by the Review Board of Nagoya City University Graduate School of Medical Sciences (approval No. 990).
DNA isolation and PCR amplification of TP53 codon 72 and MDM2 SNP 309 polymorphisms
Formalin-fixed paraffin-embedded tissue blocks were used for DNA extraction for gene amplification. Tumor samples were macrodissected from FFPE tissues blocks guided with hematoxylin-and-eosin (H&E) stained sections. Following deparaffinization with xylene and alcohol, genomic DNA was extracted using the QIAamp DNA Mini Kit (QIAGEN, Valencia, CA, USA).
The status of TP53 codon 72 (rs1042522) and MDM2 SNP 309 (rs2279744) was determined in the study participants using a TaqMan SNP Genotyping Assay. Primers were purchased from Applied Biosystems (Foster City, CA, USA). Assay ID for TP53 codon 72 (rs1042522) was C_2403545_10. Primers and probes for MDM2 SNP 309 were as follows: 5′-GACTACGCGCAGCGTTCA-3′ (forward); 5′-AGGTCTCCGCGGGAGTTC-3′ (reverse); 5′-CGCGCCGCAGCGGC-3′ (VIC); 5′-CCGCGCCGAAGCGGC-3′ (FAM).
Genotyping was performed on an Applied Biosystems 7500 FAST Real-Time PCR System using a TaqMan SNP genotyping assay (Affymetrix Inc., Cleveland, OH, USA). Each reaction (10 μL) contained 5 μL TaqMan Genotyping Master Mix, 0.5 μL primers and probes (Applied Biosystems), 3.5 μL water and 1 μL DNA (5–10 μL/μL). Thermal cycling conditions were 95°C for 10 min, followed by 50 cycles of 95°C for 15 sec and 60°C for 1 min.
IHC staining
The same tissue block used for extracting genomic DNA was selected from each case slide. Serial 3-μm thick sections were made from FFPE tissue blocks.
Tissue sections were deparaffinized and rehydrated. After heat-induced antigen retrieval, IHC was performed using an automated immunostainer (Bond-Max, Leica MicroSystems, Wetzlar, Germany) with monoclonal antibodies against TP53 (clone DO7; dilution, 1:200) and MDM2 (clone 1B10; 1:200). Nuclei were counterstained with hematoxylin. Nuclear staining of TP53 and MDM2 protein was shown as brown granules. A positive result was defined as more than 30% of the tumor cells showing positive staining.
All slides were reviewed in a blinded manner without clinical information by two independent authors (H. I. and K.M.). When the assessment was different between the two observers, agreement was reached using a double-headed microscope. These slides were observed using a light microscope (Nikon ECLIPSE 80i, Nikon Corporation Tokyo, Japan) with a 40× field objective and 10× ocular lens corresponding to a field diameter of 550 μm for the slides.
Statistical analyses
The chi-square test and Fisher’s exact test were used to assess the significance of any difference in the prevalence of TP53 codon 72 and MDM2 SNP 309 polymorphisms among PDAC, CP and normal control groups. Tests for Hardy—Weinberg equilibrium were conducted using a goodness-of-fit chi-square test to compare the observed genotype frequencies with the expected genotype frequencies using reported frequencies in Japanese populations with two degree of freedom. The odds ratio (OR) and 95% confidence intervals (CI) were used as measures of the association strength. Values of p ≤ 0.05 without the Bonferroni correction and p ≤ 0.017 with the Bonferroni correction (two comparisons between three groups) were considered statistically significant. Kaplan—Meier analysis was used to analyze overall survival period. A Cox proportional hazards analysis was also performed to identify factors that could lead to a shorter overall survival period.
Results
Patient characteristics (Table 1)
This study included 32 PDAC patients, 16 CP patients and 32 normal controls (median age, 64 years; range, 32–82 years). The patient characteristics are summarized in Table 1. No significant differences in the distribution of gender, age, body mass index (BMI), smoking, or diabetes were observed among three groups. Among PDAC patients, 14 patients (43.8%) received chemotherapy, 2 (6.3%) received radiotherapy and 5 (15.6%) received chemoradiotherapy after tumors were resected. The follow-up period ranged from 3.1 to 101.7 months (median, 23.1 months). The overall one-year survival rate was 71.9% (23/32).
Genotype frequency in each group
Detection of TP53 codon 72 and MDM2 SNP 309 polymorphisms using real—time PCR was conducted successfully in all cases. Distributions of these polymorphisms in patients and controls are shown in Figs. 1 and 2.
The p-value was calculated by comparing the Pro/Pro genotype between PDAC patients and normal controls and between CP patients and normal controls.
The p-value was calculated by comparing the G/G genotype between PDAC patients and normal controls and between CP patients and normal controls.
The genotype distribution of the TP53 codon 72 polymorphism was as follows: 21 cases (65.6%) of Pro/Pro, 9 (28.1%) of Arg/Pro and 2 (6.25%) of Arg/Arg genotypes in PDAC; 6 (37.5%) cases of Pro/Pro, 8 (50%) of Arg/Pro and 2 of (12.5%) Arg/Arg in CP; 5 (15.6%) of Pro/Pro, 16 (50.0%) of Arg/Pro and 11 (34.4%) of Arg/Arg in normal controls. The Pro/Pro genotype was more frequent in PDAC patients than in normal controls (p < 0.001; adjusted OR, 10.31; 95% CI, 3.17–33.24), whereas no significant difference of Pro/Pro frequency was observed between CP patients and controls (p = 0.144).
Conversely, MDM2 SNP 309 polymorphism showed different genotype distribution in each group as follows: 7 cases (21.9%) of GG, 14 (43.8%) of GT and 11 (34.4%) of TT genotypes in PDAC; 5 cases (31.3%) of GG, 4 (25%) of GT and 7 (43.8%) of TT in CP; 9 (28.1%) of GG, 12 (37.5%) of GT and 11 (34.4%) of TT in normal controls. The genotype frequency was not significantly different among the three groups (PDAC vs. normal, p = 0.774; CP vs. normal, p = 0.822).
The genotype frequencies reported in articles studying Japanese populations fit Hardy—Weinberg equilibrium (HWE, Table 2, 3). Therefore, we used a pooled control group reported previously for the normal Japanese population in order to investigate HWE. This step increased the number of control cases for better comparison with our results. The distribution of the TP53 codon 72 polymorphism in normal controls (χ2 = 0.571, df = 2, p = 0.752) fit HWE, while those in PDAC (χ2 = 78.95, df = 2, p < 0.001) and CP (χ2 = 10.44, df = 2, p = 0.005) did not fit HWE (Table 4). The distribution of the MDM2 SNP 309 polymorphism in PDAC (χ2 = 2.155, df = 2, p = 0.340), CP (χ2 = 4.944, df = 2, p = 0.084) and normal controls (χ2 = 2.658, df = 2, p = 0.265) fit HWE (Table 5).
Genotype effect on survival
Overall survival data of all PDAC patients were included in the survival analysis. Based on the log-rank test and Kaplan-Meier survival curve analyses, overall survival was not significantly different between Pro/Pro and other genotypes (p = 0.471; Fig. 3a). The median survival of patients with Pro/Pro and other genotypes was 638 days (95% CI, 504–978 days) and 752 days (631–1291 days), respectively.
(a) TP53 codon 72 genotypes (b) MDM2 single-nucleotide polymorphism (SNP) 309 genotypes.
By contrast, the median survival of MDM2 G/G genotype and other genotypes (T/G and T/T) were 359 days (249–722 days) and 911 days (732–1333 days), respectively. Overall survival was significantly shorter in the G/G genotypes compared with other genotypes (p = 0.016, Fig. 3b).
IHC of TP53 and MDM2 for polymorphism comparison
As shown in Fig. 4, TP53 IHC was positive in 17 of 32 PDAC patients (53.1%), 2 of 16 CP patients (12.5%) and 4 of 32 normal controls (12.5%). MDM2 IHC was positive in 11 of 32 PDAC patients (34.4%), 2 of 16 CP patients (12.5%) and 3 of 32 normal controls (9.4%). The positive expression rate of TP53 IHC was significantly more frequent in PDAC than in normal controls (vs. normal controls, p = 0.001) and the positive expression rate of MDM2 IHC was significantly more frequent in PDAC than in normal controls (p = 0.016). The positive expression rates of TP53 and MDM2 IHC in CP patients did not significantly differ from the rate in normal controls.
Although MDM2 G/G genotypes and overall survival were associated, no statistically significant differences of overall survival were observed between IHC-positive and IHC-negative PDAC patients (TP53 IHC positive vs. negative, p = 0.619; MDM2 IHC positive vs. negative, p = 0.981, Fig. 5a, b).
(a) TP53 IHC positive/negative, (b) MDM2 IHC positive/negative.
Multivariate analysis adjusted by potential confounding factors
The Cox proportional hazards model was applied to multifactor analysis using the following variables: age (<60 or ≥60 years), gender, smoking history, body mass index (BMI, <20 or ≥20), TNM staging, TP53 codon 72 genotype (Pro/Pro or not), MDM2 SNP 309 genotype (G/G or not), IHC of TP53 and MDM2, and the existence of tumor-node-metastases. The outcomes indicated that all factors, except the MDM2 G/G genotype, were not correlated with overall survival.
Discussion
Polymorphism in TP53 codon 72 produces two different P53 proteins because of a single base change altering CGC to CCC in the fourth exon of the TP53 gene, altering amino acid residue 72 from Arg to Pro [17, 18]. An association of the TP53 codon 72 polymorphism with several cancer susceptibilities has been reported [19–29]. Additionally, a common MDM2 promoter polymorphism is the T→G transformation at nucleotide 309. This MDM2 309T/G promoter polymorphism is associated with the development of a variety of tumors [4–6]. However, its association with PDAC has not been fully evaluated. Therefore, we investigated the involvement of TP53 and MDM2 in malignant transformation and disease progression. To our best knowledge, this is the first study evaluating the significance of TP53 codon 72 polymorphism using FFPE pancreatic tissue.
We confirmed that the ratio of Pro/Pro genotype was significantly more frequent in PDAC patients than in controls, even using FFPE tissues, and the finding supports the hypothesis that this polymorphism influences the TP53 gene expression. In this study, the normal controls satisfied HWE, as compared with a pooled analysis from previous articles, which indicates that they were concurrent with the general population. This result vindicates the statistical outcomes in the study. Furthermore, the Pro/Pro frequency in PDAC was higher in this study using FFPE tissues (65.6%) than in the studies of Sonoyama et al. (14.6%) [9] or Nacaeeati et al. (7.9%) [30] using blood samples. One of the plausible explanations for this finding is the influence of FFPE; however, HWE in normal controls with FFPE in this study suggests that it is unlikely. Another plausible explanation is the occurrence of a somatic mutation that is also supported by the failure to fit HWE in PDAC with FFPE tissues. The TP53 codon72 somatic mutation might play an important role in carcinogenesis or cancer progression of PDAC, as well as its germline mutation [31].
In CP, the presence of the TP53 codon 72 allele was not statistically significant. In a previous study, when using tissues obtained by endoscopic ultrasound-guided fine needle aspiration (EUS-FNA), the K-ras mutation status was considered a biomarker for PDAC [32]. Similarly, this finding, combined with the conventional cytology test, might provide more accurate diagnosis to distinguish PDAC from CP such as mass-forming pancreatitis, using only a small specimen obtained by EUS-FNA.
The difference of the MDM2 SNP 309 among the three disease groups was not statistically significant. The HWE of MDM2 SNP 309 in PDAC, CP, and normal controls indicates that few cases have a somatic mutation at this site. However, the analysis of overall survival revealed significant differences between the GG allele and GT/TT allele of SNP 309 genotypes, which was not obtained in the analysis of the TP53 codon 72 genotypes. Our results are consistent with a growing body of evidence supporting a deleterious role of the G allele in this polymorphism on disease outcome. The G allele is associated with increased affinity for Sp1 binding and higher MDM2 RNA and protein levels, weakening the role of the TP53 pathway [4]. Another study suggested the G allele of the MDM2 SNP 309 T/G polymorphism is associated with increasing risk and progression of PDAC and corresponding decrease in survival [10], which partially supports our data.
We also evaluated and compared TP53 and MDM2 protein expressions using IHC on the outcome of SNP genotypes. Our results confirmed that the positive expression rate of TP53 and MDM2 protein was significantly more frequent in PDAC than in CP patients and normal controls, and that the rate in CP was similar to that of the normal controls. Positive TP53 and MDM2 protein expression in PDAC patients was similar to previous reports [5], indicating that our findings in the present study were reliable. Furthermore, the similar distribution of IHC expression in CP patients and normal controls suggest these protein expressions in CP patients were different from PDAC patients. Therefore, based on these protein expressions, CP is not a precancerous entity.
In conclusion, our study demonstrated that the TP53 codon 72 polymorphism is potentially a genetic predisposing factor for pancreatic cancer and MDM2 SNP 309 polymorphism might be useful for predicting survival outcome in PDAC patients. These findings provide insights into the oncogenesis and molecular diagnosis of PDAC.
Supporting Information
S1 Table. Raw data in our cases.
BI, Brinkman Index; BW, body weight; BMI, body mass index.
https://doi.org/10.1371/journal.pone.0118829.s001
(XLSX)
Acknowledgments
We are indebted to Hisashi Takino, Department of Anatomic Pathology and Molecular Diagnostics, Nagoya City University Graduate School of Medical Sciences; and Yukimi Itoh, Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences for providing technical assistance with histological analysis.
Author Contributions
Conceived and designed the experiments: YH KM HI. Performed the experiments: YH SS HK YN SU AK. Analyzed the data: YH MY. Contributed reagents/materials/analysis tools: TN KH IN HO TJ. Wrote the paper: YH KM MY TN.
References
- 1. Baxter NN, Whitson BA, Tuttle TM. Trends in the treatment and outcome of pancreatic cancer in the United States. Ann Surg Oncol. 2007; 14: 1320–1326. pmid:17225980
- 2. Shaib Y, Davila J, Naumann C, El-Serag H. The impact of curative intent surgery on the survival of pancreatic cancer patients: a U.S. Population-based study. The American journal of gastroenterology. 2007; 102: 1377–1382. pmid:17403071
- 3. Zhang J, Dhakal I, Yan H, Phillips M, Kesteloot H. Trends in pancreatic cancer incidence in nine SEER Cancer Registries, 1973–2002. Ann Oncol. 2007; 18: 1268–1279. pmid:17488731
- 4. Bond GL, Hu W, Bond EE, Robins H, Lutzker SG, Arva NC, et al. A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans. Cell. 2004; 119: 591–602. pmid:15550242
- 5. Dong M, Ma G, Tu W, Guo KJ, Tian YL, Dong YT. Clinicopathological significance of p53 and mdm2 protein expression in human pancreatic cancer. World journal of gastroenterology: WJG. 2005; 11: 2162–2165. pmid:15810085
- 6. Ohmiya N, Taguchi A, Mabuchi N, Itoh A, Hirooka Y, Niwa Y, et al. MDM2 promoter polymorphism is associated with both an increased susceptibility to gastric carcinoma and poor prognosis. J Clin Oncol. 2006; 24: 4434–4440. pmid:16983111
- 7. Li D, Liu H, Jiao L, Chang DZ, Beinart G, Wolff RA, et al. Significant effect of homologous recombination DNA repair gene polymorphisms on pancreatic cancer survival. Cancer Res. 2006; 66: 3323–3330. pmid:16540687
- 8. Grochola LF, Zeron-Medina J, Meriaux S, Bond GL. Single-nucleotide polymorphisms in the p53 signaling pathway. Cold Spring Harb Perspect Biol. 2010; 2: a001032. pmid:20452958
- 9. Sonoyama T, Sakai A, Mita Y, Yasuda Y, Kawamoto H, Yagi T, et al. TP53 codon 72 polymorphism is associated with pancreatic cancer risk in males, smokers and drinkers. Mol Med Rep. 2011; 4: 489–495. pmid:21468597
- 10. Asomaning K, Reid AE, Zhou W, Heist RS, Zhai R, Su L, et al. MDM2 promoter polymorphism and pancreatic cancer risk and prognosis. Clin Cancer Res. 2008; 14: 4010–4015. pmid:18559624
- 11. Grochola LF, Muller TH, Bond GL, Taubert H, Udelnow A, Wurl P. MDM2 SNP309 associates with accelerated pancreatic adenocarcinoma formation. Pancreas. 2010; 39: 76–80. pmid:19752772
- 12. Grochola LF, Taubert H, Greither T, Bhanot U, Udelnow A, Wurl P. Elevated transcript levels from the MDM2 P1 promoter and low p53 transcript levels are associated with poor prognosis in human pancreatic ductal adenocarcinoma. Pancreas. 2011; 40: 265–270. pmid:21404460
- 13. Bartek J, Bartkova J, Lukas J, Staskova Z, Vojtesek B, Lane DP. Immunohistochemical analysis of the p53 oncoprotein on paraffin sections using a series of novel monoclonal antibodies. J Pathol. 1993; 169: 27–34. pmid:8433213
- 14. Nenutil R, Smardova J, Pavlova S, Hanzelkova Z, Muller P, Fabian P, et al. Discriminating functional and non-functional p53 in human tumours by p53 and MDM2 immunohistochemistry. J Pathol. 2005; 207: 251–259. pmid:16161005
- 15. Ammann RW. A clinically based classification system for alcoholic chronic pancreatitis: summary of an international workshop on chronic pancreatitis. Pancreas. 1997; 14: 215–221. pmid:9094150
- 16. Sarner M, Cotton PB. Classification of pancreatitis. Gut. 1984; 25: 756–759. pmid:6735257
- 17. Thomas M, Kalita A, Labrecque S, Pim D, Banks L, Matlashewski G. Two polymorphic variants of wild-type p53 differ biochemically and biologically. Mol Cell Biol. 1999; 19: 1092–1100. pmid:9891044
- 18. Dumont P, Leu JI, Della Pietra AC 3rd, George DL, Murphy M. The codon 72 polymorphic variants of p53 have markedly different apoptotic potential. Nat Genet. 2003; 33: 357–365. pmid:12567188
- 19. Fan R, Wu MT, Miller D, Wain JC, Kelsey KT, Wiencke JK, et al. The p53 codon 72 polymorphism and lung cancer risk. Cancer Epidemiol Biomarkers Prev. 2000; 9: 1037–1042. pmid:11045785
- 20. Lee JM, Lee YC, Yang SY, Shi WL, Lee CJ, Luh SP, et al. Genetic polymorphisms of p53 and GSTP1,but not NAT2,are associated with susceptibility to squamous-cell carcinoma of the esophagus. International journal of cancer Journal international du cancer. 2000; 89: 458–464. pmid:11008209
- 21. Zehbe I, Voglino G, Wilander E, Genta F, Tommasino M. Codon 72 polymorphism of p53 and its association with cervical cancer. Lancet. 1999; 354: 218–219. pmid:10421306
- 22. Soulitzis N, Sourvinos G, Dokianakis DN, Spandidos DA. p53 codon 72 polymorphism and its association with bladder cancer. Cancer letters. 2002; 179: 175–183. pmid:11888672
- 23. Kalemi TG, Lambropoulos AF, Gueorguiev M, Chrisafi S, Papazisis KT, Kotsis A. The association of p53 mutations and p53 codon 72, Her 2 codon 655 and MTHFR C677T polymorphisms with breast cancer in Northern Greece. Cancer letters. 2005; 222: 57–65. pmid:15837541
- 24. Langerod A, Bukholm IR, Bregard A, Lonning PE, Andersen TI, Rognum TO, et al. The TP53 codon 72 polymorphism may affect the function of TP53 mutations in breast carcinomas but not in colorectal carcinomas. Cancer Epidemiol Biomarkers Prev. 2002; 11: 1684–1688. pmid:12496062
- 25. Mahasneh AA, Abdel-Hafiz SS. Polymorphism of p53 gene in Jordanian population and possible associations with breast cancer and lung adenocarcinoma. Saudi Med J. 2004; 25: 1568–1573. pmid:15573180
- 26. Shen H, Zheng Y, Sturgis EM, Spitz MR, Wei Q. P53 codon 72 polymorphism and risk of squamous cell carcinoma of the head and neck: a case-control study. Cancer letters. 2002; 183: 123–130. pmid:12065086
- 27. Dong M, Nio Y, Yamasawa K, Toga T, Yue L and Harada T. p53 alteration is not an independent prognostic indicator, but affects the efficacy of adjuvant chemotherapy in human pancreatic cancer. J Surg Oncol. 2003; 82: 111–120. pmid:12561067
- 28. Tsai MH, Lin CD, Hsieh YY, Chang FC, Tsai FJ, Chen WC, et al. Prognostic significance of the proline form of p53 codon 72 polymorphism in nasopharyngeal carcinoma. Laryngoscope. 2002; 112: 116–119. pmid:11802048
- 29. Yu MW, Yang SY, Chiu YH, Chiang YC, Liaw YF, Chen CJ. A p53 genetic polymorphism as a modulator of hepatocellular carcinoma risk in relation to chronic liver disease, familial tendency, and cigarette smoking in hepatitis B carriers. Hepatology. 1999; 29: 697–702. pmid:10051470
- 30. Naccarati A, Pardini B, Polakova V, Smerhovsky Z, Vodickova L, Soucek P, et al. Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic. Carcinogenesis. 2010; 31: 666–670. pmid:20110284
- 31. Comprehensive molecular characterization of gastric adenocarcinoma. Nature. 2014; 513: 202–209. pmid:25079317
- 32. Ogura T, Yamao K, Sawaki A, Mizuno N, Hara K, Hijioka S, et al. Clinical impact of K-ras mutation analysis in EUS-guided FNA specimens from pancreatic masses. Gastrointestinal endoscopy. 2012; 75: 769–774. pmid:22284089
- 33. Sakiyama T, Kohno T, Mimaki S, Ohta T, Yanagitani N, Sobue T, et al. Association of amino acid substitution polymorphisms in DNA repair genes TP53, POLI, REV1 and LIG4 with lung cancer risk. International journal of cancer Journal international du cancer. 2005; 114: 730–737. pmid:15609317
- 34. Kiyohara C, Horiuchi T, Miyake Y, Takayama K, Nakanishi Y. Cigarette smoking, TP53 Arg72Pro, TP53BP1 Asp353Glu and the risk of lung cancer in a Japanese population. Oncology reports. 2010; 23: 1361–1368. pmid:20372852
- 35. Horikawa Y, Nadaoka J, Saito M, Kumazawa T, Inoue T, Yuasa T, et al. Clinical implications of the MDM2 SNP309 and p53 Arg72Pro polymorphisms in transitional cell carcinoma of the bladder. Oncology reports. 2008; 20: 49–55. pmid:18575717
- 36. Kuroda Y, Tsukino H, Nakao H, Imai H, Katoh T. p53 Codon 72 polymorphism and urothelial cancer risk. Cancer letters. 2003; 189: 77–83. pmid:12445680
- 37. Wu WJ, Kakehi Y, Habuchi T, Kinoshita H, Ogawa O, Terachi T, et al. Allelic frequency of p53 gene codon 72 polymorphism in urologic cancers. Japanese journal of cancer research: Gann. 1995; 86: 730–736. pmid:7559095
- 38. Kuroda Y, Nakao H, Ikemura K, Katoh T. Association between the TP53 codon72 polymorphism and oral cancer risk and prognosis. Oral oncology. 2007; 43: 1043–1048. pmid:17306604
- 39. Takeuchi S, Matsushita M, Tsukasaki K, Takeuchi N, Tomonaga M, Komatsu N, et al. P53 codon 72 polymorphism is associated with disease progression in adult T-cell leukaemia/lymphoma. British journal of haematology. 2005; 131: 552–553. pmid:16281948
- 40. Hishida A, Matsuo K, Tajima K, Ogura M, Kagami Y, Taji H, et al. Polymorphisms of p53 Arg72Pro, p73 G4C14-to-A4T14 at exon 2 and p21 Ser31Arg and the risk of non-Hodgkin’s lymphoma in Japanese. Leukemia & lymphoma. 2004; 45: 957–964.
- 41. Mabuchi F, Sakurada Y, Kashiwagi K, Yamagata Z, Iijima H, Tsukahara S. Lack of association between p53 gene polymorphisms and primary open angle glaucoma in the Japanese population. Molecular vision. 2009; 15: 1045–1049. pmid:19471604
- 42. Joshi AM, Budhathoki S, Ohnaka K, Mibu R, Tanaka M, Kakeji Y, et al. TP53 R72P and MDM2 SNP309 polymorphisms and colorectal cancer risk: the Fukuoka Colorectal Cancer Study. Japanese journal of clinical oncology. 2011; 41: 232–238. pmid:21051533
- 43. Yoneda T, Kuboyama A, Kato K, Ohgami T, Okamoto K, Saito T, et al. Association of MDM2 SNP309 and TP53 Arg72Pro polymorphisms with risk of endometrial cancer. Oncology reports. 2013; 30: 25–34. pmid:23624782
- 44. Nakashima M, Kondo S, Shimizu Y, Wakisaka N, Murono S, Furukawa M, et al. Impact of MDM2 single nucleotide polymorphism on tumor onset in head and neck squamous cell carcinoma. Acta oto-laryngologica. 2008; 128: 808–813. pmid:18568525
- 45. Sugano N, Suda T, Godai TI, Tsuchida K, Shiozawa M, Sekiguchi H, et al. MDM2 gene amplification in colorectal cancer is associated with disease progression at the primary site, but inversely correlated with distant metastasis. Genes, chromosomes & cancer. 2010; 49: 620–629.