American Journal of Epidemiology Advance Access originally published online on October 22, 2008
American Journal of Epidemiology 2008 168(11):1221-1232; doi:10.1093/aje/kwn246
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NQO1 Polymorphisms and De Novo Childhood Leukemia: A HuGE Review and Meta-Analysis
Correspondence to Neela Guha, University of California at Berkeley, Northern California Childhood Leukemia Study, 2150 Shattuck Avenue, Suite 500, Berkeley, CA 94704 (e-mail: neela{at}berkeley.edu).
Received for publication September 27, 2007. Accepted for publication July 16, 2008.
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ABSTRACT |
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TOP
ABSTRACT
GENE AND ENZYMEPolymorphisms in NQO1, a gene coding for the phase II enzyme involved in the detoxification of quinone carcinogens, have been associated with childhood leukemia in some studies, although the observed direction and magnitude of effects have been inconsistent. Therefore, the authors systematically reviewed all published reports describing the effect of NQO1 in de novo childhood leukemia and conducted a meta-analysis of 7 case-control studies that examined the association between NQO1*2 and childhood leukemia. Although a family-based study previously demonstrated overtransmission of this allele among childhood acute lymphoblastic leukemia cases, the meta-analysis showed that the presence of a NQO1*2 variant allele, which reduces the activity of the enzyme NAD(P)H:quinone oxidoreductase 1 (NQO1), had no significant effect on childhood leukemia. However, there was an increased risk associated with having at least 1 copy of the NQO1*2 allele in a subset of cases with MLL translocations (summary odds ratio = 1.39, 95% confidence interval: 0.98, 1.97). Heterogeneity between studies may be due to differences in population exposures to NQO1 substrates and small sample sizes, as well as potential population stratification in non-family-based studies. Therefore, further research is warranted on the role of NQO1 polymorphisms in the etiology of childhood leukemia, especially among MLL-positive leukemias.
epidemiology; leukemia; meta-analysis; NAD(P)H dehydrogenase (quinone); NQO1; polymorphism, single nucleotide; systematic review
Abbreviations: ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; CI, confidence interval; NQO1, NAD(P)H:quinone oxidoreductase 1; OR, odds ratio; SNP, single nucleotide polymorphism
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GENE AND ENZYME |
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The human NAD(P)H:quinone oxidoreductase 1 gene (NQO1; DT-diaphorase, Enzyme Commission (EC) number 1.6.99.2 [EC] ) occupies 17 kilobase pairs (kb) within a gene-rich region on chromosome 16 at 16q22.1 (1). This cytosolic flavoenzyme detoxifies quinones (a large class of aromatic compounds found commonly in plants, benzene metabolites, and chemotherapies) to hydroquinones or catechols (2–4). The enzyme NAD(P)H:quinone oxidoreductase 1 (NQO1) acts as an antioxidant by catalyzing a 2-electron reduction that bypasses the need for two 1-electron reductions that can result in the production of DNA and protein-damaging reactive oxygen species. In certain conditions (e.g., the presence of myeloperoxidase or autooxidants), NQO1 can contribute to the formation of reactive oxidation species via oxidative cycling and therefore can act as a prooxidant (2, 5). NQO1 is constitutively expressed in most tissues including the bone marrow, where expression is thought to be highly inducible by xenobiotics with quinone moieties, and is upregulated during times of oxidative or electrophilic stress (6). NQO1 expression is also upregulated in tumor tissues as the result of hypoxia (7): The success of quinone-based chemotherapies to exert their cytotoxic effects depends on their bioactivation by elevated levels of NQO1.
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GENE VARIANTS |
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There have been more than 93 single nucleotide polymorphisms (SNPs) identified in the NQO1 gene. The most widely studied SNP of NQO1 is a C to T change at nucleotide position 609 (rs1800566), also known as NQO1*2. This results in a proline to serine amino acid change at codon 187 that is associated with a loss of enzyme activity due to instability of the protein product (8). Thus, the enzyme activity of the homozygous variant genotype (NQO1*2/*2) is almost undetectable, and the enzyme activity of the heterozygous genotype (NQO1*1/*2) is intermediate between the homozygous variant genotype and wild type (NQO1*1/*1) (6). The NQO1*2 allele frequency varies between different ethnic groups, ranging from 16% in Caucasians to 49% in Chinese populations. Prevalence of the NQO1*2/*2 genotype is 4.4% in non-Hispanic whites, 5.2% in African Americans, 12.2% in Japanese, 15.5% in Mexican Hispanics, 17.9% in Native Americans, 18.8% in Koreans, and 22.4% in Chinese (6, 9–11).
Another genetic polymorphism of NQO1 is a single nucleotide change from C to T at nucleotide position 465 (rs4986998), also known as NQO1*3, which changes the amino acid at codon 139 from arginine to tryptophan. This SNP results in alternative messenger RNA splice sites that can lead to a deletion of exon 4 and create a protein lacking the quinone binding site (12–15) for which enzyme activity differs according to the substrate (14). The frequency of the NQO1*3 polymorphism is generally low and ranges from 0% to 5% among different ethnic populations (9).
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LABORATORY TESTS |
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Most publications describing NQO1 genotyping utilized polymerase chain reaction followed by restriction fragment length polymorphism analysis or allele-specific oligonucleotide hybridization assays, as described previously (16, 17). The SNPs on NQO1 are also amenable to genotyping by using more modern array-based methods.
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DISEASE |
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Leukemia represents one-third of all cancer cases under the age of 15 years and is the most common pediatric cancer (18). A heterogeneous disease that disrupts normal hematopoiesis, it can present as either acute or chronic: Approximately 80% of childhood leukemias (<15 years of age) are acute lymphoblastic leukemia (ALL), less than 20% are acute myeloid leukemia (AML), and 2% are chronic myeloid leukemia, while chronic lymphocytic leukemia rarely occurs in children (19).
The incidence of childhood ALL varies by and within countries, with the lowest rates observed by the African countries (from 4.5 per million to 14.3 per million), followed by Asian countries (from 9.2 per million to 40.6 per million), with the highest rates observed by European, American (North, Central, and South), and Oceania (Australia and New Zealand) countries (from 16.1 per million to 48 per million) (20). In contrast, the differences in the incidence of childhood AML among different countries are not as distinct (20). In addition, the ratio of ALL to AML also varies by region, with the lower ratios observed in most African and Asian countries (i.e., more AML than ALL cases) and higher ratios observed in the European, American, and Oceania countries (20).
The most common cytogenetic changes in childhood leukemias include high hyperdiploidy (>50 chromosomes in karyotype) and specific recurrent chromosomal translocations; these are both believed to occur in utero after prenatal exposure to toxic agents. About 80% of infant leukemia cases (acute leukemia in children <12 months of age) harbor the MLL gene rearrangement at 11q23, and the most common translocation among children aged 2–5 years is the TEL-AML1. Despite our knowledge of tumor genetics, the causes of childhood leukemia are largely unknown: Currently, the only established risk factors are ionizing radiation and genetic syndromes such as Down syndrome (21). Accordingly, exogenous factors including history of infections, maternal diet and medication use during pregnancy, and benzene exposures from pesticides, parental smoking, parental occupation, and traffic emissions have been the subject of investigation. Several compounds from these exposures can be oxidized to semiquinones and quinones by peroxidases (e.g., myeloperoxidase), which then are substrates for NQO1 (5, 22).
The NQO1*2 variant allele has been associated with infants' leukemias harboring the MLL rearrangement (17, 23), childhood ALL (16), and therapy-related leukemias (24, 25). These observations are supported by a large epidemiologic study that showed that presence of the NQO1*2 allele increased the risk of hematotoxicity more than 2-fold among a large cohort of Chinese workers exposed to benzene, an established risk factor for adult AML (26). The NQO1*3 allele has been less studied, although Eguchi-Ishimae et al. (27) showed an association with Japanese infant leukemia cases that harbored the MLL-AF4 [t(4;11)] translocation. In contrast, in a comparison of childhood leukemia cases with controls in a British population, there was no evidence of association of the NQO1*3 allele in MLL-positive leukemias in infants (odds ratio (OR) = 1.12) or in TEL-AML1 or hyperdiploid leukemias compared with controls (17).
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REVIEW AND METHODS—IDENTIFICATION AND ELIGIBILITY OF RELEVANT STUDIES |
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Our objective was to identify all published articles examining the association between NQO1 polymorphisms and childhood leukemia. We searched PubMed for all articles published up to September 24, 2007. We identified 56 articles with the search terms ("NAD(P)H Dehydrogenase (Quinone)" [MeSH] or "NQO1") and "leukemia" and limiting the search to studies in human populations. Articles with the following characteristics were excluded from the review: 1) non-English articles; 2) review articles; 3) nonepidemiologic studies (e.g., studies on animals or cell culture); 4) treatment outcome studies; 5) studies with therapy-related leukemia; 6) studies that included nonleukemia cases (e.g., non-Hodgkin's lymphoma) without reporting separate results for leukemia; and 7) studies with only adults or studies that combined adult and childhood leukemia but did not report results separately by age group (Figure 1). As of September 24, 2007, we had identified 9 published studies describing the association between NQO1 polymorphisms and de novo childhood leukemia: 1 family-based study (28) and 8 "case-control" studies (16, 17, 23, 27, 29–32) for which 2 of these studies (23, 31) included case-only analyses.
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ASSOCIATIONS |
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Family-based studies
One study with a family-based design of 657 case-parent trios and case-parent-grandparent clusters found that the NQO1*2 allele was transmitted to childhood ALL cases more frequently than expected, with a relative risk (dominant model) of 1.39 (95% confidence interval (CI): 1.07, 1.79) (28). This study also examined transmission of the NQO1*2 allele among 21 trios of infants (aged
12 months) with leukemia and found that there was a large, nonstatistically significant increased risk with carrying the variant allele (relative risk = 4.29, 95% CI: 0.58, 31.68). The family-based design is a powerful approach to study the effects of genetic variation in disease susceptibility, because it is immune to the effects of population stratification that could bias the results of case-case and case-control studies.
Case-case studies
Two studies used a case-only approach to examine the association between NQO1*2 and MLL-positive leukemias in infants (23, 31). Both studies used patients with de novo B-lineage ALL without the MLL gene rearrangement as a comparison group. The NQO1*2 allele significantly increased the risk of MLL-negative leukemia in infants in both the Italian (OR = 5.55, 95% CI: 1.81, 16.98) (31) and American (OR = 2.47, 95% CI: 1.08, 5.68) populations (23).
Case-control studies
Among the 5 traditional case-control studies that examined the association between NQO1*2 and acute childhood leukemia, the results were inconclusive (Table 1) (16, 27, 29, 31, 32). In a Canadian population, the presence of at least 1 variant NQO1*2 allele increased the risk of childhood ALL in cases compared with controls by approximately 50% (OR = 1.49, 95% CI: 1.02, 2.19) (Figure 2) (16). In contrast, a decreased risk of childhood ALL associated with the NQO1*2 allele was observed in a Turkish population (OR = 0.79, 95% CI: 0.58,1.08) (32). The other case-control studies showed essentially null results (27, 29, 31). In addition, Wiemels et al. (17) did not detect any association of the NQO1*2 allele in a subset of TEL-AML1-positive and hyperdiploid childhood ALL cases. There was no evidence of association between NQO1*2 and childhood AML among the 3 case-control studies that examined this outcome (27, 29, 32).
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Four case-control studies examined the association between NQO1*2 and MLL-positive childhood leukemia (17, 27, 30, 31). A significantly increased risk of MLL-positive leukemia associated with the NQO1*2 allele was observed in a British population (OR = 2.5, 95% CI: 1.08, 5.96) (17), while results from 2 other studies were also suggestive of an increased risk (27, 31). Additionally, in a case-control analysis comparing allele frequencies in cases with the expected population distribution of NQO1 allele frequencies at nucleotide position 609 derived from the published literature, Smith et al. (23) observed that MLL-positive leukemia cases were significantly more likely to have at least 1 copy of the NQO1*2 allele compared with ethnically matched, disease-free subjects (OR = 2.50; P = 0.02). Three of these studies further classified MLL-positive cases and identified a small subset (n
35) of cases harboring the MLL-AF4 translocation [t(4;11)] (17, 27, 30). Wiemels et al. (17) authored the only case-control study to show a significantly increased risk of MLL-AF4-positive leukemias associated with the NQO1*2 allele (OR = 8.63, 95% CI: 2.45, 33.22). It should be noted that this study (17) had the smallest sample size (21 MLL-AF4-positive cases) among all 3 studies. In summary, the results of 4 case-control studies suggest that the NQO1*2 allele may be associated with MLL-positive leukemia (17, 27, 30, 31) and possibly with the MLL-AF4-positive subtype (17). |
INTERACTIONS |
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The presence of a functional polymorphism in NQO1 does not appear to confer a strong increased risk of childhood leukemia in general but may do so in the presence of an environmental exposure to quinones. Furthermore, this effect may be modified by polymorphisms in other carcinogen-metabolizing genes such as the GSTs, CYP2E1, and MPO. Therefore, it is important to study gene-gene and gene-environment interactions. In a French study, Clavel et al. (29) examined interactions among the NQO1*2 polymorphism, maternal tobacco smoking, and alcohol and coffee consumption during pregnancy. Using a case-control analysis, they observed that maternal coffee consumption negatively interacted with the NQO1*2 allele to reduce the risk of childhood acute leukemia (OR = 0.3, 95% CI: 0.1, 1.0). However, they found no significant interactions between the NQO1*2 polymorphism and either maternal smoking or alcohol consumption during pregnancy. A case-only analysis produced similar results.
Using a trio design (biologic parents and the affected child) to study a French-Canadian population, Infante-Rivard et al. (28) did not observe a multiplicative interaction between prenatal exposure to mononuclear aromatic hydrocarbons and the child's (NQO1) genotype (likelihood ratio test: P = 0.33) but did find weak evidence for a "supermultiplicative" interaction between maternal smoking during pregnancy and the child's (NQO1) genotype (likelihood ratio test: P = 0.15). In a small sample of study subjects, Krajinovic et al. (16) found a suggestion of a combined 3-way interaction between NQO1 and CYP2E1 risk-elevating genotypes and the wild-type MPO allele in increasing the risk of childhood ALL (OR = 5.4, 95% CI: 1.2, 23.4).
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META-ANALYSIS |
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Identification and eligibility of relevant studies for meta-analysis
We decided that a quantitative summary of the role of NQO1 in childhood leukemia would be useful and therefore conducted a meta-analysis using the results of published studies. It was only possible to include case-control studies from the review into the meta-analysis because of the need for exposed and unexposed groups and diseased and nondiseased groups. Therefore, 2 of the studies included in the review were excluded from the meta-analysis because of 1) a family-based design (28) and 2) a case-only analysis of MLL-positive versus MLL-negative cases (23) (Figure 1). Although the latter study (23) included a second comparison group of disease-free, ethnically matched controls, the expected NQO1 allele frequencies were derived from previously published data and expressed as a percentage, rather than a count, and therefore could not be included in our meta-analysis. Table 1 describes the 7 case-control studies included in the meta-analysis.
Data abstraction for meta-analysis
All articles were assessed independently by two reviewers (N. G. and J. S. C.), who extracted data from each article that included authors, year of publication, country of origin, case and control selection, demographics of the study subjects, and the number of cases and controls for the genotypes of each NQO1 polymorphism. Any discrepancies between the two reviewers were resolved by discussion and consultation with a third reviewer (A. P. C.).
Statistical methods for meta-analysis
Four childhood leukemia outcomes were assessed in this meta-analysis: 1) ALL, 2) AML, 3) MLL-positive leukemia (ALL or AML), and 4) MLL-AF4-positive leukemia (ALL or AML). We calculated summary odds ratios for studies that assessed the relation between NQO1*2 and each outcome. Because NQO1*3 was assessed in only 2 studies (16, 27), we did not include this marker in the current meta-analysis. Forest plots were used to display the results from individual studies on a common scale, as well as the summary odds ratios, and further allowed for a visual assessment of the degree of heterogeneity among studies (Figures 2–5) (33). We used both random and fixed effect models with weights equal to the inverse of the variance to calculate a summary odds ratio for the effect of NQO1*2 on the different subtypes of childhood leukemia. Results from random effects models, which account for heterogeneity among studies, are presented when Mantel-Haenszel chi-squared (
2) tests for heterogeneity showed significant differences across studies (conservatively defined as P < 0.20).
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The I2 statistic measured the extent of inconsistency among the studies (34). I2 values of 25%–50% indicate moderate inconsistency, while values larger than 50% reflect large inconsistencies among studies. We assumed a dominant mode of inheritance (the presence of at least 1 variant allele vs. wild-type), because only 1 copy of the variant NQO1*2 allele is needed to reduce enzyme activity. However, to explore the possibility of a "threshold effect" of enzyme activity, we also explored the analyses for the ALL and AML subsets assuming a recessive mode of inheritance (homozygous variant vs. heterozygote + wild-type); the results were similar to those assuming a dominant model (data not shown). It should be noted that only 1 study did not separate heterozygote and homozygote variants and therefore was not amenable to assessing a recessive mode of inheritance (31).
We evaluated publication bias by using funnel plots (35); however, this assessment was uninformative because of the limited number of studies. The results of the meta-analysis were generated using RevMan software (Review Manager, version 4.2 for Windows; The Nordic Cochrane Centre, Copenhagen, Denmark, 2003). Forest plots were generated using the "plot.meta" function in R software (http://www-ice.iarc.fr/
martyn/software/meta/).
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META-ANALYSIS RESULTS |
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Overall effects
Figure 2 presents the results of the 5 previous studies examining the association between the NQO1*2 polymorphism and risk of childhood ALL by using a random effects model. Only 1 of the 5 studies showed a significant positive association between childhood ALL and the presence of at least one NQO1*2 allele (16). Overall, the summary odds ratio showed no evidence of association of the NQO1*2 variant and risk of childhood ALL (OR = 1.08, 95% CI: 0.83, 1.40).
Results of the 3 studies that examined the association between the NQO1*2 polymorphism and childhood AML are shown in Figure 3. None of the 3 individual studies showed a statistically significant association (27, 29, 32). The combined analysis, using a random effects model showed no effect of the NQO1*2 variant on the development of childhood AML (OR = 0.90, 95% CI: 0.50, 1.62). Of the studies that evaluated the relation between the NQO1*2 polymorphism and MLL-positive leukemia (ALL or AML), 3 of 4 showed a positive association (17, 27, 31) (Figure 4), but only 1 study had statistically significant results (17). The combined odds ratio of these 4 studies suggested an increased risk of MLL-positive childhood leukemia associated with the presence of at least 1 NQO1*2 allele (fixed effects model: OR = 1.39, 95% CI: 0.98, 1.97; 2 test for heterogeneity: P = 0.23). This result was also supported by that of Smith et al. (23) (not included in this meta-analysis), who showed that the NQO1*2 allele increased risk of MLL-positive leukemia (OR = 2.47, 95% CI: 1.08, 5.68).
Results of the 3 studies that examined the associations between risk of childhood ALL or AML with the MLL-AF4 translocation and the presence of the NQO1*2 allele were inconsistent (Figure 5). The combined odds ratio for these 3 studies (OR = 1.79, 95% CI: 0.49, 6.55) suggested that the presence of at least 1 NQO1*2 allele confers an increased risk of MLL-AF4-positive childhood leukemia; however, this result must be interpreted with caution as the confidence interval of the combined odds ratio is very wide and driven mainly by the results of 1 study (17).
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DISCUSSION |
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Overall, we did not find any statistically significant association of the NQO1*2 polymorphism and the risk of childhood ALL. However, a family-based study (28) using trios (biologic parents and the affected child) found that there was excess transmission of the NQO1*2 variant allele from parents to affected offspring, suggesting that the NQO1*2 variant was associated with developing childhood ALL.
When restricting to a subset of studies with MLL-positive leukemia as the outcome, we observed an elevated risk with borderline statistical significance with the presence of at least 1 variant NQO1*2 allele (17, 27, 30, 31). Smith et al. (23) also reported that infants with de novo MLL-positive leukemias were significantly more likely to be heterozygous for the NQO1*2 allele (OR = 2.77, 95% CI: 1.17, 6.57; P = 0.02) and also significantly more likely to have low/null activity NQO1 genotypes (NQO1*1/*2 or NQO1*2/*2) than patients with de novo B-lineage ALL without MLL translocations (OR = 2.47, 95% CI: 1.08, 5.68; P = 0.03). This subgroup of infants with de novo MLL-positive leukemias were also significantly more likely to have low/null activity NQO1 genotypes (NQO1*1/*2 or NQO1*2/*2) than expected in an ethnically matched population of disease-free subjects (OR = 2.50; P = 0.02) (23). The lack of statistically significant results among the MLL-positive subgroup in our meta-analysis may be due to the rare occurrence of MLL-positive leukemias in infants, but these results are biologically plausible.
A rearrangement in the MLL gene at 11q23 is common in leukemias of both infants (<2 years) and adults (as secondary leukemias that arise after chemotherapy with topoisomerase II inhibitors), suggesting that topoisomerase II inhibition may be a common mechanism (36). Many of the compounds that are metabolized by NQO1 also inhibit topoisomerase II, an enzyme involved in maintaining DNA structure through cleavage and subsequent repair of double-stranded DNA. Inhibition of topoisomerase II activity can ultimately result in chromosomal translocations, as has been evidenced by the ability of dietary flavonoids to cleave the MLL gene (37).
However, the mechanism by which MLL breakage and subsequent translocation occur still remains to be discovered: Topoisomerase II inhibition, as well as bioactivation of reactive metabolites, and formation of reactive oxygen species have been suggested. The double-stranded DNA breaks created by topoisomerase II inhibition can stimulate apoptosis, which leads to the activation of endonucleases that cause further DNA breaks. Wild-type NQO1 has been shown to sensitize cells to undergo apoptosis by tumor necrosis factor-alpha and also to stabilize the p53 tumor suppressor protein, whereas NQO1*2 does not (38, 39). Therefore, it is also possible that the NQO1*2 variant can enable cells to survive DNA damage, thereby increasing the likelihood of survival with DNA breaks and translocations.
The overall results of the meta-analysis may be biased because of confounding and population stratification that may be present in the individual case-control studies included. However, many of the case-control studies included in this meta-analysis had relatively homogeneous ethnic/racial populations (16, 17, 27, 30–32) and/or were matched for ethnicity (29).
The largely negative results among childhood leukemias (outside the MLL group) may be a reflection of low bioactivation in precursor B-cells (i.e., low myeloperoxidase) and also low relevant exposures in the pediatric population. There may also be unrecognized gene-gene and gene-environment interactions that have yet to be elucidated. The elevated risk in the MLL group and in particular the MLL-AF4 group (17, 23) suggests that the MLL gene or the AF4 gene is particularly sensitive to reactive quinones in the bone marrow. This result was not upheld in the Japanese population (27), leaving open the suggestion that the NQO1*2 allele may be linked to a second causal allele within this gene-rich region of chromosome 16 in non-Japanese populations.
Furthermore, the differences in worldwide incidence rates of childhood leukemia and the worldwide differences in the observed ratios of ALL to AML could be due to the variation of environmental exposures among regions; for example, differences in exposure profiles to infectious agents have also been suggested (40). As suggested by Kracht et al. (30), the specific exposure histories for leukemia cases may reflect differences in exposure profiles among countries.
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BIAS |
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The results of the meta-analysis were most suggestive of the role of low/null activity NQO1*1/*2 and NQO1*2/*2 genotypes in MLL-positive leukemia. Among the 4 studies included in this subgroup analysis, the study by Wiemels et al. (17) was the most influential. Therefore, we also reassessed the results by dropping this study and found weak evidence of association between NQO1*1/*2 and NQO1*2/*2 variant genotypes and MLL-positive infant leukemia (OR = 1.19, 95% CI: 0.80, 1.77).
The different choice of control groups (Table 1) could bias the results of the individual studies and lead to inconsistencies between studies; however, the direction and magnitude of this bias are uncertain. For example, hospital-based controls may not necessarily be representative of the underlying source population, and therefore population-based controls may be a better comparison group. Use of controls that are older than cases can introduce a bias because older subjects could have a very different exposure history and also a different response to toxic exposures (because of differences in body size) than younger subjects. Controls selected from different geographic areas than those of the cases can also introduce bias because the cases and controls could have different genetic ancestries and exposure histories. Lack of quality control measures used during genotyping could introduce misclassification bias from genotyping error. Furthermore, the genotyping calls could be prone to bias if the observer was not blinded to case-control status. Although we used random effects models to account for heterogeneity between studies, results from fixed effects models were similar.
We also evaluated bias in our results using 3 criteria (amount of evidence, replication, and protection from bias) published in the interim guidelines for the assessment of cumulative evidence on genetic associations (41). For the amount of evidence, all subgroup analyses (Figures 2–5) contained a moderate number of subjects studied with the NQO1*2 allele. Furthermore, there was no obvious bias incurred from phenotype misclassification or population stratification; however, there was insufficient information on quality control procedures for genotyping (Figures 2–5; Table 1). To assess replication of the associations, we used the I2 values that ranged from 30.9% to 83.3%. The totality of evidence for the association of the NQO1*2 allele with childhood leukemia, as suggested by these guidelines, is moderate for acute lymphoblastic and MLL-positive leukemia but weak for acute myeloid and MLL-AF4-positive leukemia.
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POPULATION TESTING |
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Currently there is insufficient evidence to establish the role of NQO1 in childhood leukemia and, thus, population testing for polymorphisms in this gene has not been implemented.
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OTHER POTENTIAL PUBLIC HEALTH APPLICATIONS |
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There are currently not enough data to support any public health applications.
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CONCLUSIONS AND RECOMMENDATIONS FOR RESEARCH |
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Results of studies examining the effect of polymorphisms in NQO1 on childhood leukemia have been inconsistent, and this is the first meta-analysis to systematically summarize the association of the NQO1*2 polymorphism and the risk of childhood leukemia by immunophenotypic and cytogenetic subtype, when possible. A more homogeneous and consistent classification of the outcome would increase statistical power to detect any significant associations. Therefore, future studies should also cytogenetically classify leukemia cases. Such efforts will understandably require large numbers of patients to assess statistically meaningful cytogenetic subgroups, requiring coordinated collaboration among epidemiology study groups.
We conclude that the NQO1*2 variant allele appears to have no strong association with childhood ALL or AML, but it may be associated with MLL-positive childhood leukemias. However, these results should be interpreted with caution, as this meta-analysis included only a few studies with small sample sizes. Furthermore, the suggested increase in risk of MLL-positive childhood leukemia among the NQO1*2 allele carriers was driven mainly by the results of 1 case-control study but was also supported by 1 additional case-only study. This emphasizes the need for further replication of these findings. Because this is a rare subtype, this would be a prime candidate for a consortium-based effort.
Because the presence of a functional polymorphism in NQO1 may not confer an increased risk of childhood leukemia alone, but rather in the presence of an environmental exposure to quinones, in future studies it would also be important to incorporate both the effects of environmental agents and genotypes of other enzymes (e.g., GSTs, CYP2E1, MPO) that metabolize these carcinogenic substances to toxic quinones and reactive oxygen species (22). Such investigations will require larger sample sizes to permit assessment of first- and, possibly, second-order interactions.
Some of the heterogeneity between the risk ratios of individual studies may simply be a result of unmeasured cofactors that vary among the populations studied here; therefore, inconsistent results between studies warrant detailed exploration. Because NQO1*2 is a highly penetrant marker and metabolizes a number of putative leukemogens, it remains an important candidate risk factor for leukemia and deserves further analysis.
Our meta-analysis of case-control studies did not provide evidence for a statistically significant effect of NQO1*2 in childhood ALL, yet a family-based study (28) did demonstrate an overtransmission of NQO1*2 among ALL cases. These conflicting results underscore the need to incorporate genetic markers of ancestry for addressing the bias that may result from potential population stratification in non-family-based study designs (i.e., case-control studies), especially given the wide population differences in NQO1*2 allele frequencies (42–44). In addition, family-based designs such as case-parent trios should be encouraged (44, 45). Future studies are needed in Asians and Hispanics, populations that have a higher occurrence of the NQO1*2 polymorphism, in order to better understand its role in childhood leukemia in these populations. In addition, other SNPs in NQO1—such as the less-studied C465T functional variant (NQO1*3), other haplotype-tagging SNPs, and SNPs in neighboring genes—should be further evaluated to comprehensively assess the importance of NQO1 in the development of childhood leukemia.
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ACKNOWLEDGMENTS |
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Author affiliations: Division of Epidemiology, School of Public Health, University of California, Berkeley, California (Neela Guha, Anand P. Chokkalingam, Patricia A. Buffler); Department of Epidemiology and Biostatistics, University of California, San Francisco, California (Jeffrey S. Chang, Joseph L. Wiemels); and Division of Environmental Health Sciences, School of Public Health, University of California, Berkeley, California (Martyn T. Smith).
A. P. C. and P. A. B. were supported by grant R01 ES09137. J. S. C. was supported by a fellowship from the National Cancer Institute (grant R25 CA 112355). M. T. S. was supported by National Institutes of Health (NIH) Superfund grant P42ES04705. J. L. W. is a Scholar of the Leukemia and Lymphoma Society and was supported by NIH grant CA89032.
The authors thank Sébastien Antoni for assistance with formatting the figures.
Conflict of interest: none declared.
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NOTES |
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Editor's note: This paper is also available on the website of the Human Genome Epidemiology Network (http://www.cdc.gov/genomics/hugenet/).
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N. Guha, J. S. Chang, A. P. Chokkalingam, J. L. Wiemels, M. T. Smith, and P. A. Buffler THE AUTHORS REPLY Am. J. Epidemiol., May 15, 2009; 169(10): 1279 - 1279. [Full Text] [PDF]
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M. Lanciotti and C. Dufour Re: "NQO1 POLYMORPHISMS AND DE NOVO CHILDHOOD LEUKEMIA: A HUGE REVIEW AND META-ANALYSIS" Am. J. Epidemiol., May 15, 2009; 169(10): 1278 - 1279. [Full Text] [PDF]
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