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Marijuana Use and Risk of Oral Squamous Cell Carcinoma

¹ Department of Community Health, University of Illinois at Urbana-Champaign, Champaign, Illinois; ² Program in Epidemiology, Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington; ³ Department of Epidemiology, School of Public Health and Community Medicine, University of Washington, Seattle, Washington; and ⁴ Center for Health Studies, Group Health Cooperative, Seattle, Washington

	ABSTRACT

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Previous laboratory investigations, case reports, and a hospital-based case-control study have suggested that marijuana use may be a risk factor for squamous cell head and neck cancer. We conducted a population-based case-control study to determine whether marijuana use is associated with the development of oral squamous cell carcinoma (OSCC). Case subjects (n = 407) were 18–65-year-old residents of three counties in western Washington State who were newly diagnosed with OSCC from 1985 through 1995. Control subjects (n = 615), who were similar to the cases with respect to age and sex, were selected from the general population using random-digit telephone dialing. Lifetime histories of marijuana use and exposure to known OSCC risk factors were ascertained using a structured questionnaire. Information on genetic polymorphisms in glutathione S-transferase enzymes was obtained from assays on participant DNA. Odds ratios for associations with features of marijuana use were adjusted for sex, education, birth year, alcohol consumption, and cigarette smoking. A similar proportion of case subjects (25.6%) and control subjects (24.4%) reported ever use of marijuana (adjusted odds ratio, 0.9; 95% confidence interval, 0.6–1.3). There were no trends in risk observed with increasing duration or average frequency of use or time since first or last use. No subgroup defined by known or suspected OSCC risk factors (age, cigarette smoking, alcohol consumption, and genetic polymorphisms) showed an increased risk. Marijuana use was not associated with OSCC risk in this large, population-based study.

	INTRODUCTION

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Marijuana is the most commonly used illegal drug in the United States (1) , and new users increased among minors during the 1990s (2) . Marijuana smoke contains many known carcinogens (3) , and experimental studies show that components of marijuana smoke are mutagenic in bacteria (4 , 5) and cause molecular and cellular changes in bronchial tissue comparable with those seen among tobacco smokers and consistent with early steps in cancer development (6, 7, 8) . Such findings raise the possibility that chronic marijuana use could cause premalignant changes in cells throughout the upper aerodigestive tract.

The possibility that marijuana use might be a risk factor for head and neck squamous cell carcinoma (HNSCC) was initially raised by several case reports (9) . A small hospital-based study of HNSCC cases (n = 173) and blood donor controls (n = 176) found that ever users of marijuana were at >2-fold increased risk of HNSCC [odds ratio (OR), 2.6; 95% confidence interval (CI), 1.1–6.6] and that the risk increased with increasing frequency of marijuana use (10) . Because hospital-based studies may be particularly susceptible to biases when lifestyle characteristics are the focus of investigation, we analyzed data from a population-based study to test the hypothesis that marijuana use is a risk factor for oral squamous cell carcinoma (OSCC).

	MATERIALS AND METHODS

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Study Population.
This report is based on participants, data, and biological specimens assembled during two population-based case-control studies originally designed to examine the association between human papillomavirus infection and OSCC risk (11 , 12) . All participants were residents of King, Pierce, or Snohomish counties, Washington State. Eligible cases in the first study were all 18–65-year-old men diagnosed with first, incident OSCC between January 1985 and December 1989. Eligible cases in the second study include all 18–65-year-old men and women diagnosed with first, incident OSCC between January 1990 and June 1995. OSCC patients were ascertained through the population-based Cancer Surveillance System, a participant in the Surveillance, Epidemiology, and End Results program (14) . In both studies, only individuals who could communicate in English were eligible. OSCC was defined as in situ and invasive tumors of the tongue, gums, floor of mouth, tonsils, oropharynx, and other intraoral sites. In the earliest of the two studies (11) , the definition of OSCC also included cancers of the lip (exclusive of the vermilion border); these cases of lip cancer were excluded from the present report. To be eligible, OSCC cases also were required to have residential telephones to ensure comparability with controls, who were identified for both previous studies through random-digit telephone dialing and frequency-matched to cases on age (18–19 years, 20–24 years, 25–29 years, ... , 60–65 years) and sex. The protocols for recruitment of cases and controls in both studies were approved by the institutional review board of the Fred Hutchinson Cancer Research Center.

Combined across the two studies, 407 cases and 615 controls participated in an in-person interview (see below). These figures represented participation rates for cases in the first and second study of 54.4% and 63.3%, respectively, and 59.7% overall. Only eligible cases and controls were included in calculation of participation rates. Among the 275 nonparticipating cases in the previous two studies, 125 had died before they could be contacted for recruitment. The control response rates for the two studies were 63% and 61%, respectively; these rates incorporate both the household screening phase of random-digit telephone dialing and the success at interviewing eligible controls from among screened households.

Data and Biological Specimen Collection.
Participating cases and controls were interviewed in-person by trained personnel using a structured questionnaire. The same questionnaire was used in both studies. To elicit histories of marijuana use, we initially asked each participant whether he or she had ever smoked marijuana or hashish (a stronger form of marijuana). If a participant had ever smoked these substances, he or she was asked about different episodes of marijuana or hashish use during his or her lifetime, with each episode representing a different frequency of use (elicited in terms of times per day, week, month, or year). For each episode, each participant was asked about the frequency of use, the age (in whole years) he or she started and stopped using marijuana or hashish at that frequency, and whether marijuana, hashish, or both substances were used. The interview also elicited demographic characteristics and extensive histories of tobacco use and alcohol consumption as described previously (13) . All questions were directed toward the time period before each participant’s reference date. The reference date for a case was the month and year he or she was diagnosed. Reference dates for controls were assigned at random from among the possible case diagnosis dates that had occurred before the selection of a particular control through random-digit telephone dialing.

Genetic Polymorphism Analyses.
Because the putative carcinogenicity of marijuana may derive, at least in part, from exposure to polycyclic aromatic hydrocarbons and other tobacco-related carcinogens, we assayed for polymorphisms in several glutathione S-transferase (GST) genes (GSTM1, GSTT1, and GSTP1), which are known to be involved in the biotransformation of these compounds. Biological specimens from which genomic DNA could be extracted had been sought from each participating case and control during the original studies (13) . Across the two studies, such specimens were available for 365 of 407 interviewed cases (89.7%) and 576 of 615 interviewed controls (93.7%). The null polymorphisms of GSTM1 and GSTT1 were assayed as described previously (15 , 16) . The GSTP1 (I105V) polymorphism (http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi?rs=947894) was assayed as follows: a 176-bp fragment was amplified using primers 5'-ACC-CCA-GGG-CTC-TAT-GGG-AA-3' and 5'-TGA-GGG-CAC-AAG-AAG-CCC-CT-3'. Each 30-µl reaction contained 15 µl of Qiagen Taq PCR Master Mix, 0.2 µM each primer, and 100 ng of genomic DNA. Thermal cycling conditions were as follows: 1 cycle at 94°C for 5 min; 40 cycles at 94°C for 2 min, 60°C for 1 min, and 72°C for 2 min; and 1 cycle at 72°C for 5 min. BsmA1 (New England Biolabs) restriction fragments were separated on a 4% nusieve gel.

Quality control samples included wells containing known genotype (positive controls), wells with PCR reagent only (negative controls), and paired replicate aliquots. Two reviewers independently read the gels and assigned genotypes without knowledge of the case-control status or other characteristics of each participant. Genetic analyses, which were restricted to whites because of variation in allele frequency across racial groups and because most of our study population was white (92.4% among controls), included the following numbers of subjects (percentage of total interviewed): GSTM1, 340 cases (89.0%) and 548 controls (83.5%); GSTT1, 339 cases (88.8%) and 547 controls (83.3%); and GSTP1, 355 cases (91.5%) and 565 controls (87.2%).

Statistical Analysis.
We created variables to characterize various features of marijuana use, including ever use, time since first use, time since last use, years of use, and average frequency of use. The average frequency of use was calculated by first determining, for each episode, the number of times the participant had used marijuana (based on the length of the episode and the reported frequency of use). We then summed the total number of uses over each participant’s lifetime and divided that number by the total weeks of use. These quantitative measures of the extent of marijuana use were categorized for analyses. A separate exposure category, with respect to each of these measures, was established for participants whose who had <1 year of use because this exposure level was felt to be minimal and could not be distinguished from years since first use or years since last use (i.e., because their reported age at first and last use of marijuana was the same). The remaining categories used for marijuana use were established so that they represented either 5- or 10-year intervals (years of use, years since first use, years since last use) or could be directly compared with the results of Zhang et al. (times used/week; Ref. 10 ). Participants who reported never using marijuana comprised the referent group for comparisons.

We used standard methods for statistical analysis of case-control studies (17) . ORs and 95% CIs were calculated using unconditional logistic regression. Analyses were adjusted for sex, education, birth year (continuous), average drinks of alcohol/week (continuous), pack-years of cigarette smoking (continuous), and whether the data came from the first (11) or second (12) of the previous studies. We assessed whether the data were consistent with effect measure modification between marijuana use and other characteristics (age, sex, cigarette smoking, alcohol consumption, and genetic polymorphisms) by estimating stratum-specific ORs associated with marijuana use and by estimating ORs jointly for marijuana use and each putative modifier relative to a common baseline consisting of individuals who never used marijuana and were in the a priori "low-risk" category of the modifier. We performed likelihood ratio tests of the fit of respective models with multiplicative and additive interaction terms compared with the fit of models without such terms. For multiplicative models, all terms were log-linear, whereas for additive models, confounders were log-linear, and the interaction terms were linear. Possible differences in the association with marijuana use according to tumor site (tongue, gum, floor of the mouth, tonsils and hypopharynx, and other sites) were assessed using polytomous logistic regression (18) .

To evaluate the extent to which the reporting of marijuana use among our controls was consistent with other population-based studies, we analyzed publicly available data from the National Household Survey of Drug Abuse (NHSDA) conducted in 1988 and 1990–1994 [the NHSDA was not conducted in 1989) (19) ]. These years largely include the reference dates we used for eliciting risk factor histories. We compared the observed number of controls who reported ever use of marijuana with the expected number, based on the birth cohort (or in some analyses, age) and sex-specific prevalences of "ever marijuana use" from the NHSDA and the birth cohort and sex-specific distribution of our controls. We calculated the observed:expected ratio of ever marijuana users and corresponding 95% CIs using the logarithmic transformation.

	RESULTS

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Cases had lower annual incomes and a lower educational level than controls (Table 1) . The risk of OSCC was strongly related to cigarette smoking and alcohol consumption, as well as the combination of these characteristics (results not shown).

	DISCUSSION

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In this large, population-based study, we did not find any association between marijuana use and OSCC risk. The absence of an increased risk was largely consistent across analyses using different measures of marijuana use (e.g., ever use, frequent versus infrequent use, and long-term versus short-term use) and among subgroups representing different levels of underlying risk.

The possibility that marijuana use might increase the risk of cancer was initially raised more than 20 years ago when marijuana smoke components yielded positive results in Ames salmonella/microsome mutagenesis assays (4 , 5) . However, in other non-human model systems, ⁹-tetrahydrocannabinol, the psychoactive component of marijuana, both induced expression, and inhibited the activity, of cytochrome p450 1A1 (3) ; the combination of tobacco extracts and ⁹-tetrahydrocannabinol also led to reduced cytochrome p450 1A1 activity. In studies focusing directly on tumor development and growth, cannabinoids have been shown to have both tumorigenic (20 , 21) and antitumor (22 , 23) properties. These findings suggest that the ultimate effect of marijuana use on OSCC development, if any, results from opposing physiological pathways. Nonetheless, human in vivo studies of chronic marijuana smokers have found increased premalignant changes in bronchial tissue (8 , 24) akin to those observed in lung tissue from tobacco smokers.

Reports of young patients with OSCC and other respiratory tract cancers raised the question of whether marijuana use contributed to these malignancies (9) . These reports lacked comparison groups and control for established risk factors and thus provide little evidence for or against the existence of an association. A cohort study did not provide results specific to OSCC or HNSCC, but for lung cancer and other smoking-related and/or alcohol-related cancers in general, no association was found (25) . The only epidemiological study of marijuana use and HSNCC found a 2–3-fold increased risk associated with ever marijuana use, a dose-response relationship with frequency and duration of use, and evidence of particularly strong associations with ever use among several subgroups [e.g., younger individuals, smokers, and those exhibiting mutagen sensitivity (10) ]. Although our study had a greater proportion of participants who had used marijuana for >5 years [10.9% versus 3.5% in Zhang et al. (10) ], we did not confirm their findings.

Differences in the extent to which control groups represent the population from which the cases arise potentially explain the discrepancy between our null findings and the increased risks observed by Zhang et al. (10) . Blood donors comprise a highly self-selected population likely to be depleted of individuals with high-risk lifestyle behaviors; thus, the prevalence of marijuana use by blood donor controls in Zhang et al. (10) may have been spuriously low in comparison with what would have been observed in a group of controls that more closely reflected the source population for their cases. Alternatively, as Zhang et al. (10) hypothesized, controls may in general underreport marijuana use to a greater extent than cases. Zhang et al. (10) used published NHSDA estimates (26) to show that the observed prevalence of ever marijuana use among their controls was similar to the prevalence expected in the general population (10) . The published data from which Zhang et al. (10) calculated expected numbers, however, excluded persons who had initiated marijuana use after 20 years of age (Table 5 in Ref. 10 ; Table 3 in Ref. 26 ), whereas the observed number of users among their controls included individuals who had used marijuana regardless of the age at initiation. We recalculated the sex- and birth cohort-adjusted expected prevalence of ever marijuana use among controls in Zhang et al. (10) without the exclusion based on age at initiation (using publicly available NHSDA data for individuals who were 18 years old in 1992–1994). The expected number of ever marijuana users was 40.6, whereas only 17 users were observed. If a similar deficit was not present among the HNSCC cases in Zhang et al. (10) , some or all of the 2.6-fold association with marijuana use they observed would be due to a spuriously low exposure prevalence among their controls. The results of similar calculations performed for our control group showed no difference in the observed and expected number of ever marijuana users.

Marijuana cigarettes do not contain filters, as tobacco cigarettes do, and are typically smoked well into the proximal end. Furthermore, marijuana smokers may inhale more deeply and hold the smoke in their lungs longer than tobacco smokers (27 , 28) . These latter characteristics of marijuana smoking may explain why lung tar levels are higher for marijuana cigarettes compared with tobacco cigarettes (29) . If marijuana is an oral cavity carcinogen, we nonetheless may not have observed an association because the amount of marijuana consumed by a typical user is substantially less than the amount of tobacco consumed by a typical tobacco smoker (1) , and a substantial proportion of our population were not chronic, long-term users of this drug. We also did not ask about the number of marijuana cigarettes or bowls of hashish smoked or the depth of inhalation.

Our study included only OSCC, whereas laryngeal carcinomas comprised a large proportion (27%) of the cases in Zhang et al. (10) . Marijuana use was reported similarly by their laryngeal cancer cases (22%) and tongue carcinoma cases (approximately 19%), and we found no evidence that the marijuana use association varied by OSCC site. Potential etiologic heterogeneity among HNSCC of different organs thus does not seem to explain the differences between our results and those of Zhang et al. (10) .

Our study was not without important limitations. We had relatively low participation, and any association between marijuana use and participation status that differed between cases and controls could have biased our results. If an association between marijuana use and OSCC truly exists, but the prevalence of marijuana use among our controls is close to that expected (as discussed above), then under-recruitment of cases who had used marijuana or under-reporting of marijuana use by cases due to the drug’s illegality could have led to our null associations. Our study observed well-established associations with tobacco smoking and alcohol drinking, however, providing some reassurance that low participation among our cases has not noticeably affected our study. Our study also did not have data on mutagen sensitivity status, which Zhang et al. (10) found to be a strong modifier of the risk associated with marijuana use. Because Zhang et al. (10) observed an association between HNSCC and marijuana use even without considering mutagen sensitivity status, we also should have observed an association if the prevalence of mutagen sensitivity among our participants was similar to that in Zhang et al. (10) .

Studies of HNSCC have not observed consistent associations with the GSTM1-null, GSTT1-null, or GSTP1 I105V polymorphisms (30, 31, 32, 33, 34) , but few have examined whether these polymorphisms modify the risk associated with exposure to sources of carcinogens that the enzymes metabolize. We did not find that carriers of the "high-risk" genotypes of GSTM1, GSTT1, or GSTP1 who also smoked marijuana were at greater risk than predicted on a multiplicative or additive scale. Marijuana use was associated with a borderline statistically significant 50% reduced risk of OSCC among individuals carrying at least one copy of the GSTM1 gene, statistically distinguishable from the absence of an association among GSTM1-null homozygotes. The reduced risk of OSCC among carriers of GSTM1 could represent a chance finding or could be consistent with induction of detoxifying GSTM1 activity by marijuana constituents. Although we also observed statistically distinguishable heterogeneity in the association with marijuana use among current, former, and never cigarette smokers, the pattern of ORs did not fit any obvious biologically based model, nor was similar effect modification seen with pack-years of cigarette smoking. In general, our study was not sufficiently large to allow us to reliably assess the potential modifying effects of known or suspected OSCC risk factors on risks associated with marijuana use.

Although the evidence from nonepidemiological investigations suggests that marijuana smoking could cause upper respiratory tract cancer, we did not observe an association with OSCC in this study. Nonetheless, because our data included relatively few individuals who had used marijuana for many years, we cannot discount the possibility that long-term use of this drug is related to OSCC risk. As individuals born since the 1940s age into their sixth decade of life (when the baseline rates of OSCC start to rise dramatically), the prevalence of long-term use marijuana use in the population will increase. This demographic change will permit future studies to assess more definitively the role of marijuana in OSCC development.

	FOOTNOTES

 
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.

Requests for reprints: Stephen M. Schwartz, Program in Epidemiology, Fred Hutchinson Cancer Research Center, M4-C308, P. O. Box 19024, Seattle, WA 98109-1024. E-mail: sschwart{at}fhcrc.org

Received 11/ 2/03. Revised 3/11/04. Accepted 3/23/04.

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