Piepoli A, Gentile A, Valvano MR, Barana D, Oliani C, Cotugno R, Quitadamo M, Andriulli A, Perri F. Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients. World J Gastroenterol 2006; 12(39): 6343-6348
Corresponding Author of This Article
Dr Ada Piepoli, Research Laboratory Department of Gastroenterology, “Casa Sollievo della Sofferenza” Hospital, IRCCS, San Giovanni Rotondo, Italy. email@example.com
Article-Type of This Article
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients
Ada Piepoli, Annamaria Gentile, Maria Rosa Valvano, Daniela Barana, Cristina Oliani, Rosa Cotugno, Michele Quitadamo, Angelo Andriulli, Francesco Perri
Ada Piepoli, Annamaria Gentile, Maria Rosa Valvano, Rosa Cotugno, Michele Quitadamo, Angelo Andriulli, Francesco Perri, Unit and Research Laboratory of Gastroenterology, “Casa Sollievo della Sofferenza”, Hospital, IRCCS, San Giovanni Rotondo, Italy
Daniela Barana, Cristina Oliani, Department of Medical Oncology, Hospital and University of Verona, Verona, Italy
Cristina Oliani, Oncology Unit, ULSS5 Ovest Vicentino, Verona, Italy
ORCID number: $[AuthorORCIDs]
Supported by the Italian Ministry of Health, grant No. RC0402GA19
Correspondence to: Dr Ada Piepoli, Research Laboratory Department of Gastroenterology, “Casa Sollievo della Sofferenza” Hospital, IRCCS, San Giovanni Rotondo, Italy. firstname.lastname@example.org
Telephone: +39-882-416281 Fax: +39-882-411879
Received: March 29, 2006 Revised: September 8, 2006 Accepted: September 9, 2006 Published online: October 21, 2006
AIM: To investigate simultaneously UGT1A7, UGT1A9, ARP, SPINK and CFTR genes to verify whether genetic polymorphisms predispose to the development of pancreatic cancer (PC).
METHODS: Genomic DNA of 61 pancreatic cancer patients and 105 healthy controls (HC) were analyzed. UGT1A7 genotyping was determined by PCR-RFLP analysis. Specific PCR and sequencing were used to analyze genetic variants of UGT1A9, ARP, SPINK1 and CFTR genes.
RESULTS: Four different alleles (*1: WT; *2: N129K and R131K; *3: N129K, R131K, and W208R; and *4: W208R) in UGT1A7 and three different alleles (*1: WT; *4: Y242X; and *5: D256N) in UGT1A9 were detected. All UGT1A polymorphisms were observed at similar frequency in PC patients and HC. Seven different alleles in ARP were found in PC patients and HC at similar frequency. The SPINK1 mutations N34S and P55S occurred in five PC patients with a prevalence (4.1%) not significantly different from that observed (2.0%) in HC. The only CFTRΔF508 mutation was recognized in three PC patients with a prevalence (4.9%) similar to HC.
CONCLUSION: UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms are not associated with PC in Italian patients.
Citation: Piepoli A, Gentile A, Valvano MR, Barana D, Oliani C, Cotugno R, Quitadamo M, Andriulli A, Perri F. Lack of association between UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms and pancreatic cancer in Italian patients. World J Gastroenterol 2006; 12(39): 6343-6348
Pancreatic cancer (PC) is still a major cause of morbidity and mortality worldwide. Despite extensive research, its etiology remains elusive. Recent data suggest that both genetic and environmental factors play a role in the development and progression of PC.
In 5%-10% of cases, PCs are inherited either as part of a known familial cancer syndrome or in association with familial forms of chronic pancreatitis; in contrast, in 90%-95% of PC cases, the relationship between possible genetic predisposition and environmental risk factors is less clear. Tobacco smoking is actually recognized as the only environmental risk factor in at least 30% of all sporadic PC, while the role of alcohol and other xenobiotics is still controversial.
Polymorphisms in low penetrance genes involved in carcinogen metabolism and oxidative stress, such as CYP1A1, CYP2D6, GSTM1, GSTT1, NAT1, UGT1A7 and UGT1A9, could increase susceptibility to PC through exposure to endogenous metabolites or environmental xenobiotics. Interestingly, among all these detoxifying activities, the UGT1A7 and UGT1A9 seem to be the only enzymes capable of tobacco-borne toxicant inactivation[4-6]. Only few studies have investigated the polymorphism of UGT1A7 and UGT1A9 genes in PC patients with controversial findings[7,8].
The known pancreatic cancer susceptibility genes include germline mutations of high penetrance tumor suppressor genes or oncogenes involved in cell cycle control and DNA repair such as CDKN2A (also known as p16), p53, DPC4 (also known as SMAD4), STK11, BRCA2, K-ras, hMLH1 and arginine-rich protein (ARP). The effect of these gene mutations in inducing PC seems to be poorly influenced by environmental factors. In particular, ARP gene has been described as oncogene. Although the functional role of the encoded protein is still unknown, the gene has been found in all species and is highly conserved at the DNA and RNA level. The presence of multiple AGG repeats around codon 50 of the mRNA and the gene has been reported in a variety of solid tumors[10,11]. Thus, variations in the ARP trinucleotide repeat region correspond to polymorphisms of the gene.
The known familial chronic pancreatitis susceptibility genes include germline mutations of moderate penetrance genes, such as cationic trypsinogen (PRSS1), serine protease inhibitor Kazal type 1 (SPINK1)[14-16] or cystic fibrosis transmembrane conductance regulator (CFTR) which determine hereditary pancreatitis (HP), idiopathic chronic pancreatitis (ICP) and cystic fibrosis (CF), respectively. These genes are involved in trypsinogen activation and chloride transport, cause long-standing chronic pancreatitis and, in combination with other environmental factors such as smoking, may induce PC. However, when the polymorphisms of these genes were investigated in patients with PC, data have been inconclusive[18,19].
We hypothesize that patients with PC could have an asymptomatic chronic pancreatitis due to the interaction of environmental factors (smoking and other xenobiotics) and genetic variations of genes involved in chronic pancreatitis susceptibility or detoxifying activities (i.e. UGT1A7). Moreover is conceivable that these genes may interact with each other and with other known risk factors (i.e. smoking) thus increasing the risk for PC. A possible explanation of the inconclusive results of the previous studies could be the evaluation of polymorphisms of single gene. This study focused on the simultaneous investigation of the genetic variations in UGT1A7, UGT1A9, ARP, SPINK1 and CFTR genes as potential risk factor for sporadic PC in an Italian population cohort. A possible gene-gene interaction and correlation with age at diagnosis and smoking habit was also evaluated.
MATERIALS AND METHODS
We investigated the prevalence of UGT1A7, UGT1A9, ARP, SPINK1 and CFTR gene polymorphisms in 61 consecutive unrelated patients with sporadic pancreatic adenocarcinoma (PC) (mean age: 63 ± 10 years; range: 44-81 years; male/female: 31/30) and in 105 healthy blood donors (HC) (mean age: 39 ± 9 years; range: 19-60 years). Information on histological diagnosis and tumor location were available for all patients with pancreatic cancer (Table 1). DNA from patients and controls was obtained from peripheral blood samples after written informed consent was given. The study was approved by the Ethics Committee of our hospital.
Table 1 Clinical features of pancreatic cancer patients.
Pancreatic cancer patients
n = 61
Mean age ± SD (range) (yr)
63 ± 10 (44-81)
31 (50.8%)/30 (49.2%)
Primary tumor location
38 (62.3%) 15 (24.6%)
18 (29.5%)/43 (70.5%)
Genotyping of UGT1A7 (MIM: 606432)
UGT1A7 exon 1 polymorphic variants were identified by PCR-RFLP methods, as described by van der Logt et al. Briefly, to detect variations at UGT1A7 codons 129/131, we used the forward primers F1 and F2 and the reverse primer R1 (Table 2). F1 only detects the N129K/R131K polymorphism, whereas F2 detects both the N129K/R131K and N129R/R131K polymorphisms. To detect the W208R alteration, we used the forward primer F3 and the reverse primer R2 (Table 2). To determine whether the N129K/R131K or N129R/R131K and W208R occur cis or trans, we used the primers F4 and R1 (Table 2). PCR conditions were 5 min at 95°C, then 37 cycles of 45 s at 95°C, 45 s at 55°C (codons 129/131)/65°C (codon 208) /56°C (allele specific), and 45 s at 72°C, and finally an elongation step at 72°C for 5 min. Aliquots of 10 µL of the PCR product were digested with the restriction enzyme VspI (codons 129/131) or RsaI (codon 208/allele specific) for at least 1 h at 37°C.
Table 2 Primers and restriction enzymes used for genotyping analyses.
1Bold ‘a’ in the primer sequence denotes site-directed mutagenesis for introduction of a VspI restriction site in the wild-type allele.
Genotyping of UGT1A9 (MIM: 606434)
The strategy used to identify polymorphisms in the UGT1A9 was PCR amplification of the exon 1, followed by direct DNA sequencing. UGT1A9 exon 1 sequences were amplified using a 5’ primer that specifically anneals to sequence upstream of the UGT1A9 (GenBank accession number S55985) first exon, which is unique to the UGT1A9 gene. Specific primers (Table 2) were used to amplify a PCR product of 939 bp. The PCR conditions were 3 min at 94°C, then 30 cycles of 94°C for 30 s, 57°C for 30 s, and 72°C for 60 s. The UGT1A9 was sequenced on both strands for all subjects. The sequence of the PCR products was determined by automated sequencing and analysed by using Sequencing Analysis 3.4.1 (Applied Biosystems, Applera, Foster City, CA).
Genotyping of ARP (MIM: 601916)
PCR amplification of the (AGG) repeats around codon 50 of the ARP gene was performed using two primers, G and I (Table 2), and analyzed by both sequencing and genotyping assay. For genotyping assay, forward primer was labelled with fluorescent 6-FAM dye (provided by MWG-Biotech AG). Enzymatic amplification of DNA was performed using AmpliTaq Gold® DNA Polymerase (Applied Biosystems, Applera) and amplification cycles consisted of 10 min at 94°C, followed by 35 cycles run at 94°C for 45 s, 62°C for 75 s and 72°C for 45 s, and a final extension step of 72°C for 10 min. The PCR products were analyzed for sequence by using Sequencing Analysis 3.4.1, and for genotyping by using Genescan (Applied Biosystems, Applera, Foster City, CA).
Genotyping of SPINK1 (MIM: 167790)
The SPINK1 polymorphisms in exon 3 were determined by automatic sequencing. PCR-RFLP (restriction endonuclease: TaaI, MBI Fermentas, Germany) or PCR-CTPP (PCR with confronting two pair primers) assays were used to confirm the N34S and P55S variants.
Genotyping of CFTR (MIM: 602421)
The 31 most frequent mutations were examined by an oligonucleotide ligation assay (OLA kit, Applied Biosystems, Applera, Foster City, CA), whereas other seven mutations, frequently observed in Italian cystic fibrosis patients were examined by sequencing as previously described.
The Hardy-Weinberg equilibrium was tested by using the Arlequin software. Comparison of allele and genotype frequencies of UGT1A7, UGT1A9, ARP, SPINK1 and CFTR polymorphism was evaluated using the Monte Carlo approach with CLUMP program for the presence of multiple allele variants.
Univariate analysis was performed for tumor location, age at diagnosis and smoking habits by sorting patients according to their genotype distribution using the SPSS statistical package (SPSS v13 Inc. Chicago, IL, US). Continuous variable was expressed as means and standard deviations. Comparison of variables was performed with ANOVA method. Categorical variables were reported as percentage and comparison of them was performed by χ2-test or Fisher exact test when appropriate.
Sample size calculation to detect a significant difference between two allelic frequencies was carried out based on data reported by Ockenga et al. The software package available as shareware on the World Wide Web at http://statpages.org/proppowr.html was used to determine the sample size. We hypothesized an allelic frequency of 20% and 35% (difference proportion rate: 15%) in controls and pancreatic cancer patients. Setting the power of the test at 80% with a significance level of 5% and assuming a relative sample size proportion of 0.6 between pancreatic cancer patients and controls, we calculated a sample size of 198 alleles for controls and 119 alleles for patients. Consequently, we decided to recruit at least 100 controls and 60 pancreatic cancers into our study.
A summary of the demographic characteristics of the study population is shown in Table 1. In five subjects the diagnosis was made on clinical ground; the remaining 56 cases were confirmed histologically as ductal adenocarcinoma. In 62.3% of patients the tumor was located in the head of the pancreas, in 24.6% in the body, and in 13.1% in the tail at the time of diagnosis.
For each of the five genes, the distribution of the allele frequencies among the control population was found to fit with the assumption of the Hardy-Weinberg equilibrium (P > 0.05).
Three mutations (N129K, R131K, and W208R) combined into four different alleles (*1: wild type; *2: carrying N129K and R131K; *3: carrying N129K, R131K and W208R; and *4: carrying only W208R) were detected in the UGT1A7 gene. UGT1A7 genotyping did not show a significantly different distribution of previous alleles among patients compared to healthy controls except for the genotype *2*3 more commonly observed in healthy controls [21.0% vs 6.6%; CLUMP (T3): χ2 = 6.05, P = 0.01]. Nevertheless, after 1000 simulations with CLUMP this difference became insignificant (Pc = 0.07) (Table 3). Most notably, the frequency of the UGT1A7*3 risk allele was comparable between patients (42.6%) and controls (42.0%) (P = NS).
Table 3 Allele and genotype frequencies of UGT1A7 and UGT1A9 gene polymorphisms in pancreatic cancers and controls n (%).
Cases (n = 61)
Controls(n = 105)
UGT1A7 (exon 1)
CLUMP (T1): χ2 = 5.66 (df = 3), P = 0.10
CLUMP (T3-column used 2): χ2 = 4.75 (df = 1), Pc = 0.07 (uncorrected P = 0.03)
CLUMP (T1): χ2 = 9.43 (df = 9), P = 0.21
CLUMP (T3-column used 5): χ2 = 6.05 (df = 1), Pc = 0.07 (uncorrected P = 0.01)
UGT1A9 (exon 1)
CLUMP (T1): χ2 = 1.19 (df = 2), P = 0.79
CLUMP (T1): χ2 = 1.19 (df = 5), P = 0.79
Two variations (Y242X and D256N) combined into three different alleles (*1: wild type; *4: Y242X; *5: D256N) were detected in the UGT1A9 gene. The distribution of the UGT1A9*1, UGT1A9*4 and UGT1A9*5 alleles did not differ in PC patients and controls (Table 3). The variations were observed only in heterozygous state in both patients and controls.
In ARP gene a high frequency of genetic changes in the multiple arginine-coding-area such as M50R substitution (14.9% vs 11.1%), insertion of (AGG)n (1.4% vs 1.1%), deletion of (AGG)n (2.7% vs 4.4%) was observed in both PC and HC, respectively. Thus, we genotyped this variable site as a simple tandem repeat (STR) polymorphism. Seven different alleles (*1: 143 bp; *2: 146 bp; *3: 149 bp; *4: 152 bp; *5: 155 bp; *6: 158 bp; *7: 176 bp) were detected with wild type sequence corresponding to allele *3 and the other allele to either deletion or insertion of trinucleotide repeats. We did not observe significant difference in both allele and genotype frequencies of ARP between PC patients and HC (Table 4).
Table 4 Allele and genotype frequencies of ARP, SPINK1 and CFTR gene polymorphisms in pancreatic cancers and controls.
Cases(n = 61)
Controls(n = 105)
CLUMP (T1): χ2 = 5.25 (df = 6), P = 0.52
CLUMP (T1): χ2 = 5.29 (df = 27), P = 0.54
SPINK1 (exon 3)
CLUMP (T1): χ2 = 2.36 (df = 2), P = 0.29
CLUMP (T1): χ2 = 2.40 (df = 5), P = 0.30
CLUMP (T1): χ2 = 0.11 (df = 1), P = 1.0
CLUMP (T1): χ2 = 0.11 (df = 2), P = 1.0
Direct sequencing of the coding exonic and flanking intronic sequence of the exon 3 of SPINK1 detected mutations in 5 (4.1%) out of 61 patients. Four of them carried a heterozygous N34S mutation, and one patient had a heterozygous P55S mutation (Table 4). In 4 (2.0%) out of 105 controls two heterozygous mutations in both N34S and P55S (P = NS) were detected.
For the CFTR, only the ∆F508 mutation was found in a heterozygous state in 3 patients with PC (prevalence rate 2.5%) and in 4 controls (3.8%) (P = NS) (Table 4).
The statistical analysis was also performed after sorting pancreatic cancer patients out according to the histological type of the tumor, age at diagnosis and smoking habit. No statistically significant difference in genotype distribution of gene polymorphisms was observed (data no shown). Moreover, no evidence of interaction between investigated genes was found.
The link between genetic polymorphisms of UGT1A, UGT1A9, ARP, SPINK1 and CFTR genes and PC represent an attractive model combining genetic predisposition with environmental exposure. In the present study, we performed a simultaneous analysis of all these five genes in patients with sporadic pancreatic carcinoma. Our working hypothesis was that the predisposition to pancreatic cancer could be due to a gene-gene interaction.
Oxidative cellular injury is a prominent mechanism that could induce pancreatic inflammation and lead to genotoxicity and cancer. A major family of proteins that play a role in cellular detoxification and defense are the UDP-glucuronosyltransferase, which are expressed in different tissues with xenobiotic contact and have been implicated in chemical carcinogenesis[7,27]. Moreover, recent findings indicate that the presence of UGT polymorphisms may modify the risk of cancer development and reinforce the critical role of this pathway in the regulation of the biological activity of endogenous molecules and in determining the response to toxic chemicals. In the present study we found that the frequency of genetic polymorphisms in UGT1A7 in PC patients was not different from those of healthy controls. In particular, the frequency of the UGT1A7*3 allele encoding less active enzymes was 42.6% in pancreatic cancer compared to 42% in healthy controls, a figure comparable to that reported by Verlaan et al in patients with pancreatic disease (35%-48%) and healthy controls (41%), thus suggesting that individuals bearing this allele are not at a higher risk of developing PC. Two polymorphisms of the UGT1A9 gene (UGT1A9*4 and UGT1A9*5), described only in Japanese population[28-30], were found at a similar frequency in PC and healthy controls (0%-1%).
ARP gene has been described as a possible oncogene responsible for PC. Although the functional role of the encoded protein is still unknown, the gene was found evolutionarily conserved. To examine the involvement of the ARP gene in exocrine PC, we screened genetic variations around multiple AGG repeats and STR polymorphism present in exon 1. We did not find a difference in mutation frequency between PC patients and controls, well in keeping with Tanaka et al, who found that the frequency for wild-type, M50R substitution, (AGG)2 insertion, and AGG deletion amounted to 82%, 14%, 3% and 1%, respectively. No significant difference in allele and genotype frequencies between PC and controls for STR polymorphism were observed.
Recently, SPINK1 polymorphisms and CFTR mutations have been associated with long standing chronic pancreatitis[32,33]. SPINK1 is a potent protease inhibitor that is thought to specifically inactivate intrapancreatic trypsin. Evidence suggests that SPINK1 may act as a protective mechanism by preventing the activation of the pancreatic digestive enzyme cascade. Mutations in CFTR may disturb the subtle balance between proteases and their inhibitors by intrapancreatic acidification or by a defective apical trafficking of zymogen granules that might facilitate the intrapancreatic activation of digestive enzymes and result in pancreatitis[35,36]. In the current study, we observed that the prevalence of the SPINK1 N34S and P55S polymorphisms was similar between PC patients and healthy controls as previously reported in Caucasian sporadic pancreatic cancer groups. Regarding the frequency of the most common CFTR mutations, we found a similar prevalence of the ΔF508 mutation in PC patients and HC, consistent with similar results reported by Malats et al.
To the best of our knowledge, this is the first study to evaluate the prevalence of all five gene polymorphisms potentially involved in patients with exocrine pancreatic cancer. The findings of this study suggest that these polymorphisms are possibly not implicated in pancreatic cancer risk, although this study was powered to detect a difference proportion rate of at least 15% in allelic frequencies between controls and pancreatic cancer patients. Moreover, no gene-gene interaction or correlation with tumor location, age at diagnosis and smoking habit could be demonstrated. Further studies are needed to explore other polymorphisms involved in the metabolism of carcinogens and/or endogenous factors.
S- Editor Pan BR L- Editor Zhu LH E- Editor Liu WF
Klein AP, Hruban RH, Brune KA, Petersen GM, Goggins M. Familial pancreatic cancer.Cancer J. 2001;7:266-273.
Lowenfels AB, Maisonneuve P, Whitcomb DC, Lerch MM, DiMagno EP. Cigarette smoking as a risk factor for pancreatic cancer in patients with hereditary pancreatitis.JAMA. 2001;286:169-170.
Malats N. Gene-environment interactions in pancreatic cancer.Pancreatology. 2001;1:472-476.
Ren Q, Murphy SE, Zheng Z, Lazarus P. O-Glucuronidation of the lung carcinogen 4-(methylnitrosamino)-1- (3-pyridyl)-1-butanol (NNAL) by human UDP-glucuronosyltransferases 2B7 and 1A9.Drug Metab Dispos. 2000;28:1352-1360.
Kuehl GE, Murphy SE. N-glucuronidation of nicotine and cotinine by human liver microsomes and heterologously expressed UDP-glucuronosyltransferases.Drug Metab Dispos. 2003;31:1361-1368.
Zheng Z, Park JY, Guillemette C, Schantz SP, Lazarus P. Tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with orolaryngeal cancer risk.J Natl Cancer Inst. 2001;93:1411-1418.
Ockenga J, Vogel A, Teich N, Keim V, Manns MP, Strassburg CP. UDP glucuronosyltransferase (UGT1A7) gene polymorphisms increase the risk of chronic pancreatitis and pancreatic cancer.Gastroenterology. 2003;124:1802-1808.
Verlaan M, Drenth JP, Truninger K, Koudova M, Schulz HU, Bargetzi M, Künzli B, Friess H, Cerny M, Kage A. Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases.J Med Genet. 2005;42:e62.
Shridhar V, Rivard S, Shridhar R, Mullins C, Bostick L, Sakr W, Grignon D, Miller OJ, Smith DI. A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.Oncogene. 1996;12:1931-1939.
Shridhar R, Shridhar V, Rivard S, Siegfried JM, Pietraszkiewicz H, Ensley J, Pauley R, Grignon D, Sakr W, Miller OJ. Mutations in the arginine-rich protein gene, in lung, breast, and prostate cancers, and in squamous cell carcinoma of the head and neck.Cancer Res. 1996;56:5576-5578.
Shridhar V, Rivard S, Wang X, Shridhar R, Paisley C, Mullins C, Beirnat L, Dugan M, Sarkar F, Miller OJ. Mutations in the arginine-rich protein gene (ARP) in pancreatic cancer.Oncogene. 1997;14:2213-2216.
Evron E, Cairns P, Halachmi N, Ahrendt SA, Reed AL, Sidransky D. Normal polymorphism in the incomplete trinucleotide repeat of the arginine-rich protein gene.Cancer Res. 1997;57:2888-2889.
Whitcomb DC, Gorry MC, Preston RA, Furey W, Sossenheimer MJ, Ulrich CD, Martin SP, Gates LK Jr, Amann ST, Toskes PP. Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.Nat Genet. 1996;14:141-145.
Chen JM, Mercier B, Audrezet MP, Ferec C. Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis.J Med Genet. 2000;37:67-69.
Pfützer RH, Barmada MM, Brunskill AP, Finch R, Hart PS, Neoptolemos J, Furey WF, Whitcomb DC. SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis.Gastroenterology. 2000;119:615-623.
Pfützer RH, Whitcomb DC. SPINK1 mutations are associated with multiple phenotypes.Pancreatology. 2001;1:457-460.
Cohn JA, Friedman KJ, Noone PG, Knowles MR, Silverman LM, Jowell PS. Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.N Engl J Med. 1998;339:653-658.
Masamune A, Mizutamari H, Kume K, Asakura T, Satoh K, Shimosegawa T. Hereditary pancreatitis as the premalignant disease: a Japanese case of pancreatic cancer involving the SPINK1 gene mutation N34S.Pancreas. 2004;28:305-310.
Malats N, Casals T, Porta M, Guarner L, Estivill X, Real FX. Cystic fibrosis transmembrane regulator (CFTR) DeltaF508 mutation and 5T allele in patients with chronic pancreatitis and exocrine pancreatic cancer. PANKRAS II Study Group.Gut. 2001;48:70-74.
van der Logt EM, Bergevoet SM, Roelofs HM, van Hooijdonk Z, te Morsche RH, Wobbes T, de Kok JB, Nagengast FM, Peters WH. Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk.Carcinogenesis. 2004;25:2407-2415.
Vogel A, Kneip S, Barut A, Ehmer U, Tukey RH, Manns MP, Strassburg CP. Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene.Gastroenterology. 2001;121:1136-1144.
Witt H, Luck W, Hennies HC, Classen M, Kage A, Lass U, Landt O, Becker M. Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis.Nat Genet. 2000;25:213-216.
Hamajima N, Saito T, Matsuo K, Kozaki K, Takahashi T, Tajima K. Polymerase chain reaction with confronting two-pair primers for polymorphism genotyping.Jpn J Cancer Res. 2000;91:865-868.
Perri F, Piepoli A, Stanziale P, Merla A, Zelante L, Andriulli A. Mutation analysis of the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the cationic trypsinogen (PRSS1) gene, and the serine protease inhibitor, Kazal type 1 (SPINK1) gene in patients with alcoholic chronic pancreatitis.Eur J Hum Genet. 2003;11:687-692.
Schneider S, Roessli D, Excoffier L. Arlequin version 2.000: a software for population genetics data analysis. Geneva, Switzerland: Genetics and Biometry Laboratory, University of Geneva 2000; .
Sham PC, Curtis D. Monte Carlo tests for associations between disease and alleles at highly polymorphic loci.Ann Hum Genet. 1995;59:97-105.
Tukey RH, Strassburg CP. Human UDP-glucuronosyltransferases: metabolism, expression, and disease.Annu Rev Pharmacol Toxicol. 2000;40:581-616.
Saeki M, Saito Y, Jinno H, Sai K, Komamura K, Ueno K, Kamakura S, Kitakaze M, Shirao K, Minami H. Three novel single nucleotide polymorphisms in UGT1A9.Drug Metab Pharmacokinet. 2003;18:146-149.
Jinno H, Saeki M, Saito Y, Tanaka-Kagawa T, Hanioka N, Sai K, Kaniwa N, Ando M, Shirao K, Minami H. Functional characterization of human UDP-glucuronosyltransferase 1A9 variant, D256N, found in Japanese cancer patients.J Pharmacol Exp Ther. 2003;306:688-693.
Girard H, Court MH, Bernard O, Fortier LC, Villeneuve L, Hao Q, Greenblatt DJ, von Moltke LL, Perussed L, Guillemette C. Identification of common polymorphisms in the promoter of the UGT1A9 gene: evidence that UGT1A9 protein and activity levels are strongly genetically controlled in the liver.Pharmacogenetics. 2004;14:501-515.
Tanaka H, Shimada Y, Harada H, Shinoda M, Hatooka S, Imamura M, Ishizaki K. Polymorphic variation of the ARP gene on 3p21 in Japanese esophageal cancer patients.Oncol Rep. 2000;7:591-593.
Drenth JP, te Morsche R, Jansen JB. Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis.Gut. 2002;50:687-692.
Sharer N, Schwarz M, Malone G, Howarth A, Painter J, Super M, Braganza J. Mutations of the cystic fibrosis gene in patients with chronic pancreatitis.N Engl J Med. 1998;339:645-652.
Frossard JL, Pastor CM. Experimental acute pancreatitis: new insights into the pathophysiology.Front Biosci. 2002;7:d275-d287.
Freedman SD, Blanco P, Shea JC, Alvarez JG. Mechanisms to explain pancreatic dysfunction in cystic fibrosis.Med Clin North Am. 2000;84:657-64, x.
Frossard JL. Trypsin activation peptide (TAP) in acute pancreatitis: from pathophysiology to clinical usefulness.JOP. 2001;2:69-77.
Teich N, Schulz HU, Witt H, Böhmig M, Keim V. N34S, a pancreatitis associated SPINK1 mutation, is not associated with sporadic pancreatic cancer.Pancreatology. 2003;3:67-68.