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Cancer Epidemiology Biomarkers & Prevention 17, 661, March 1, 2008. doi: 10.1158/1055-9965.EPI-07-2647
© 2008 American Association for Cancer Research
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NAT2*7 Allele Is a Potential Risk Factor for Adult Brain Tumors in Taiwanese Population

H. Eugene Liu1,3, Pei-Yu Hsiao2, Ching-Chen Lee5, Jen-Ai Lee2 and Hsiang-Yin Chen2,4

1 Graduate Institute of Clinical Science and 2 School of Pharmacy, Taipei Medical University; Departments of 3 Medicine and 4 Pharmacy, Taipei Medical University-Wanfang Hospital; 5 Department of Pathology, Hsin-Kong Wu Ho Su Hospital, Taipei, Taiwan

Requests for reprints: Hsiang-Yin Chen, School of Pharmacy, Taipei Medical University, 250, Wushing Street, Taipei, Taiwan 116, People's Republic of China. Phone: 886-2-55583019; Fax: 886-2-55583019. E-mail: shawn{at}tmu.edu.tw


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Arylamine N-acetyltransferase-2 (NAT2) displays extensive genetic polymorphisms that affect the rates of acetylation of drugs and toxic compounds such as amine carcinogens. The association of NAT2 polymorphisms with adult brain tumors has been unclear. To investigate whether the NAT2 genotype is a risk factor of brain tumors, we determined the frequencies of three common polymorphisms in the NAT2 gene, NAT2*5 (T341C), NAT2*6 (G590A), and NAT2*7(G857A), in brain tumor patients and in age- and gender-matched control subjects (n = 27 in each group). Genotyping was carried out using PCR-RFLP and subjects were phenotyped as a fast or slow acetylator based on the genotypes. The odds ratio of NAT2*7 allele frequency was significantly higher in patients with brain tumor than in controls (odds ratio, 6.786; 95% confidence interval, 2.06-22.37; P = 0.003); in the mean time, NAT2*4/*7 genotype was significantly more common in the patient group than in controls (odds ratio, 6.19; 95% confidence interval, 1.68-22.79; P = 0.0039). The tumors in the patients with NAT2*7 allele tended to be high-grade astrocytoma or glioblastoma multiforme (P = 0.016). In conclusion, these data suggest that the presence of NAT2*7 allele might be a potential risk factor for the development of brain tumors in Taiwan. (Cancer Epidemiol Biomarkers Prev 2008;17(3):661–5)


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
The N-acetylation polymorphism causes individual variations in the metabolism of xenobiotics with a primary aromatic amine or a hydrazine structure. N-acetyltransferase-2 (NAT2), one of the two NAT isoenzymes in humans, is responsible to the well-known inherited individual variation in the ability to acetylate arylamine agents, including polycyclic aromatic hydrocarbon in diesel exhaust and 4-aminobiphenyl and 2-naphthaylamine in cigarette smoke (1). NAT2 is expressed in the liver, colonic, and bladder mucosa. Its role in the etiology of bladder cancer has been suggested in multiple studies (2-4). Slow acetylator phenotypes caused by polymorphisms in NAT2 gene confer a higher risk of bladder cancer due to the reduced activity in the hepatic N-acetylation pathway, which detoxifies compounds such as 4-aminobiphenyl and competes with N-oxidation of these compounds by cytochrome P4501A2 to reactive hydroxylamines. The relationship between the polymorphism of NAT2 and other cancers such as lung and colorectal cancer has also been studied (5-11).

Human brain cells also express NAT2 enzymes (12). Although the brain is partially protected from chemical insults by blood-brain barrier, several drugs and pollutants can reach the brain. Therefore, NAT2 activity due to gene polymorphism could affect the risk of developing primary brain tumors. However, previous studies of NAT2 polymorphisms on brain tumors on Caucasians have been inconclusive. Two studies found no association between NAT2 acetylator status and brain tumors (9, 13). However, the other study reported that a higher number of rapid acetylation phenotype was found in brain tumor patients compared with healthy volunteers (14). Furthermore, the association of NAT2 polymorphisms with brain tumors in Asian population has not been studied. The present study was to analyze the association between NAT2 genetic polymorphisms and the risk of brain tumors in Taiwanese population. The results indicated that the patients with NAT2*4/*7 genotype were significantly at risk of developing brain tumors, although no association was found between the phenotypes of NAT2 and the overall survival. This trend suggests that, like bladder and lung cancer, genetic factors might as well play a role in developing brain tumors in our population.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Study Subjects
The baseline characteristics of 27 primary brain tumor patients (19 males and 8 females) from Hsin-Kong Wu Ho Su Hospital are shown in Table 1 . Of the 27 tumor samples, 2 were grade 1 astrocytomas, 3 grade 2 astrocytomas, 7 grade 3 astrocytomas, 11 glioblastoma multiforme, 2 oligodendrogliomas, and 2 meningiomas. Peripheral blood samples from 27 age- and gender-matched controls without the history of brain tumors were also collected in Wanfang Hospital after obtaining informed consent. The use of human tissues and record review for research purpose has been approved by the Institutional Review Board in Taipei Medical University-Wanfang Hospital and Shin Kong Wu Ho-Su Hospital.


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  		Table 1. Comparison of brain tumor patients and controls

 
PCR-RFLP Analysis for Determination of NAT2 Genotypes
Genomic DNA from paraffin-embedded tissues from brain tumor patients was extracted by commercial kits (DEXPAT). Genomic DNA from peripheral blood mononuclear cells was extracted by proteinase K digestion followed by the conventional phenol/chloroform method. Analyses for mutations at the NAT2 gene locus were done by the use of RFLP after nested PCR using the scheme shown in Fig. 1 . Primer sequences are showed in Table 2 . PCR products were subjected to the restriction enzyme digested by KpnI, TaqI, and BamHI, respectively. The digested products were resolved by 6% PAGE. NAT2*4 represents the wild-type allele and the loss of restriction cutting sites, KpnI, TaqI, and BamHI, denoted as NAT2*5 (T341C), NAT2*6 (G590A), and NAT2*7 (G857A) allele, respectively. Individuals with one or two wild-type NAT2*4 alleles were defined as fast acetylators and those with any two polymorphic alleles as slow acetylators.


Figure 1
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  		Figure 1. Schema for amplification of NAT2*5 (T341C), NAT2*6 (G590A), and NAT2*7 (G857A) by nested PCR.

 

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  		Table 2. Primer sequences used in NAT2 genotyping

 
Statistical Analysis
The difference in the phenotypes, genotypes, and variant allele frequencies in patients and normal controls were compared by using the {chi}2 test. The continuous data was compared by Student's t test. The survival analysis was done by log-rank tests (SPSS 13.0 for Windows; SPSS). A two-tailed P < 0.05 was considered statistically significant.


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
The NAT2 genotypes of the 27 brain tumor patients and the 27 age- and gender-matched normal controls were examined firstly by PCR-RFLP methods and their corresponding phenotypes were determined (Table 1). Representative results are shown in Fig. 2 . The comparison of genotypes and phenotypes for the two groups was shown in Table 1. The distributions of genotypes for the two groups were significantly different (P = 0.014), with higher percentage of patients with NAT2*4/*7 genotype than those in controls (P = 0.0039; odds ratio, 6.19; 95% confidence interval, 1.68-22.79), suggesting that this genotype might be a potential risk factor for brain tumors. Further analysis showed that the frequency of brain tumor patients with at least one NAT2*7 allele was significantly higher than the control ones (odds ratio, 6.786; 95% confidence interval, 2.06-22.37; P = 0.003; Table 2). Stratified by the histology types and pathologic grading of the tumors, patients with NAT2*7 allele were significantly more likely to have high-grade astrocytomas and glioblastoma multiforme than patients without NAT2*7 allele (P = 0.016; Table 3 ). However, the presence of NAT2*7 allele did not affect either the progression-free survival or the overall survival (Table 3).


Figure 2
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  		Figure 2. PCR-RFLP analysis for NAT2 genetic polymorphisms. After nested PCR amplification, products were subjected to a digestion with (A) KpnI for NAT2*5 allele and (B) TaqI for NAT2*6 allele and BamHI for NAT2*7 allele. Restriction enzyme-digested products were loaded onto a 6% polyacrylamide gel. Representative results for various polymorphisms.

 

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  		Table 3. Characteristics of brain tumor patients with and without NAT2*7 allele

 
There was no difference in the distribution of acetylator status between brain tumor patients and normal controls (P = 0.513; Table 1). The relationships between acetylator phenotypes and mean age of patients, tumor types, tumor grades, or the survival were further evaluated and none of these tumor characteristics was associated with NAT2 phenotypes (Table 4 ; Fig. 3 ). Twenty of 27 (74.07%) patients had fast acetylator phenotypes and 7 (25.93%) had slow acetylator phenotypes. Similar to prior studies on the NAT2 genotypes in Chinese population, 22 of healthy controls are fast acetylators and 5 are slow acetylators (15).


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  		Table 4. Comparison of fast and slow acetylators with brain tumor

 

Figure 3
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  		Figure 3. Survival curves in patients with fast and slow acetylator phenotypes. A. Progression-free survival. B. Overall survival.

 

   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
The present study examined the relationship between NAT2 genotypes/phenotypes and the risk of brain tumors. The results indicated that there is no difference in frequencies of phenotypes, the NAT2 acetylator status, between the tumor patients and the control group. The phenotype results are in agreement with studies included patients with gliomas without further classification (9, 13) but in contrast to another study with astrocytoma and meningioma patients (14). However, previous three studies did not further analyze the data of genotypes and allele frequency. Interestingly, the genotype results of the current study indicated, for the first time, that the NAT2*7 allele, particularly NAT2*4/*7 genotype, was associated with increased risk of brain tumors in Taiwanese population. Patients with NAT2*7 allele are also more likely to develop high-grade astrocytoma or glioblastoma multiforme. This finding may further provide the answer to the discrepancy of the phenotypes data between studies. The significant differences in phenotypes are only found in more malignant types of astrocytoma and glioblastoma. The results on genotype, allele frequency, and tumor grades all indicated that NAT2*7 allele, particularly NAT2*4/*7 genotype, may be a risk factor of brain tumor.

How the presence of a NAT2*7 allele affects the brain tumor risk is still unclear. However, it is not surprising that certain genotypes are associated with increased risk of developing cancer, but the case of phenotypes is another story. One study from Egypt has shown that NAT2*5/*5 genotype has been associated with increased risk of schistosomiasis-associated bladder cancer (16). Similarly, an association between bladder cancer and the presence of NAT1*10 allele has also been reported in some studies (17, 18). In lung cancer studies, although the association between lung cancer and NAT phenotype is weak, patients with NAT1*14, NAT1*15, and NAT2*5B/*6 genotypes have increased cancer risk (19, 20). Likewise, NAT1*10 allele has been found to be associated with colorectal cancer and head and neck cancer (21, 22). Further studies are required to elucidate whether these nucleotide differences represent altered chromosomal stability in a tissue-specific manner in the presence of genotoxic agents in the environment rather than changes in enzymatic activities.

Because cancer is a multigene disease, another speculation, wherein genotypes could be a risk factor, is that multiple genetic factors might take part in carcinogenesis at different stages of cancer development. Taking lung cancer as an example, although NAT2 acetylator phenotype alone is not associated with an increased risk, NAT2 genotypes, when combined with other genetic factors such as NAT1, GSTM1, or CYP1, may increase the cancer risk. Individuals, with combined NAT1 rapid and NAT2 slow genotype, seemed to have a significantly higher risk for lung adenocarcinoma (23), or the NAT2 slow genotype when combined with the GSTM1-null genotype may increase the susceptibility to adduct formation, gene mutation, and lung cancer risk (24). Similarly, a combination of NAT2 slow/CYP1A1 rapid acetylator may also predispose higher risk to lung cancer in nonsmoking females (11). Although there is no single polymorphism able to predict the risk of brain tumors, an allelic combination could jointly affect the risk of brain tumors (13, 25). Because the development of diseases is an outcome of interactions between human genes and environment, the presence of environmental agents, including toxins, might variably, possibly, and preferentially affect genetic activity among different human populations. It is not surprising that results on the association between NAT2 acetylator phenotypes or genotypes and cancers are often dependent on populations studied. Therefore, we speculate that NAT2*4/*7 or NAT2/*7 allele might take part in the complex interactions between environmental agents and cellular activities in Asian genetic background, all of which together impart increased risks for brain tumors. Although our study is somewhat limited by a small sample size, our results strongly suggest that genetic factors might play a role in the development of brain tumors especially for those with high-grade pathology in Taiwanese population and warrant further studies on the pathogenesis of brain tumors.


   Footnotes
 
Grant support: Department of Health, Center of Excellence for Clinical Trial and Research (DOH96-TB-B-111-002) in Selected Specialty.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received 10/ 3/07; revised 11/27/07; accepted 12/ 5/07.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online