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Genetic Determinants of UV-Susceptibility in Non-Melanoma Skin Cancer

  • Marleen M. Welsh,

    Affiliation Department of Preventive Medicine and Biometrics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America

  • Margaret R. Karagas,

    Affiliations Department of Community and Family Medicine, Dartmouth Medical School, Lebanon, New Hampshire, United States of America, Norris Cotton Cancer Center, Dartmouth Medical School, Lebanon, New Hampshire, United States of America

  • Jacquelyn K. Kuriger,

    Affiliation Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States of America

  • Andres Houseman,

    Affiliations Department of Community Health, Brown University, Providence, Rhode Island, United States of America, Center for Environmental Health and Technology, Brown University, Providence, Rhode Island, United States of America

  • Steven K. Spencer,

    Affiliation Department of Medicine, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States of America

  • Ann E. Perry,

    Affiliation Department of Pathology, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, United States of America

  • Heather H. Nelson

    hhnelson@umn.edu

    Affiliations Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States of America, Division of Epidemiology and Community Health, University of Minnesota, Minneapolis, Minnesota, United States of America

Genetic Determinants of UV-Susceptibility in Non-Melanoma Skin Cancer

  • Marleen M. Welsh, 
  • Margaret R. Karagas, 
  • Jacquelyn K. Kuriger, 
  • Andres Houseman, 
  • Steven K. Spencer, 
  • Ann E. Perry, 
  • Heather H. Nelson
PLOS
x

Abstract

A milieu of cytokines and signaling molecules are involved in the induction of UV-induced immune suppression and thus the etiology of non-melanoma skin cancer (NMSC). Targeting the UV-induced immunosuppression pathway, and using a large population based study of NMSC, we have investigated the risk associated with functional variants in 10 genes (IL10, IL4, IL4R, TNF, TNFR2, HTR2A, HRH2, IL12B, PTGS2, and HAL). The most prominent single genetic effect was observed for IL10. There was increasing risk for both basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) with increasing number of variant IL10 haplotypes (BCC: ptrend = 0.0048; SCC: ptrend = 0.031). Having two IL10 GC haplotypes was associated with increased odds ratios of BCC and SCC (ORBCC = 1.5, 95% CI 1.1–1.9; ORSCC = 1.4, 95% CI 1.0–1.9), and these associations were largely confined to women (ORBCC = 2.2, 95% CI 1.4–3.4; SCC: ORSCC = 1.8, 95% CI 1.1–3.0). To examine how combinations of these variants contribute to risk of BCC and SCC, we used multifactor dimensionality reduction (MDR) and classification and regression trees (CART). Results from both of these methods found that in men, a combination of skin type, burns, IL10, IL4R, and possibly TNFR2 were important in both BCC and SCC. In women, skin type, burns, and IL10 were the most critical risk factors in SCC, with risk of BCC involving these same factors plus genetic variants in HTR2A, IL12B and IL4R. These data suggest differential genetic susceptibility to UV-induced immune suppression and skin cancer risk by gender.

Introduction

While difficult to measure precisely due to lack of inclusion in national cancer registries, the incidence of non-melanoma skin cancers (NMSCs) in the US is estimated to have matched that of all other cancers combined in 2005 [1] and has been increasing dramatically over the last 25 years [2], with greater increases in women than in men. While predisposing risk factors for NMSC include pigmentation, gender, arsenic or ionizing radiation exposure, and genetic disorders such as Xeroderma pigmentosum and basal cell nevus syndrome [3], exposure to ultraviolet radiation (UVR) is arguably the most important to the development of NMSC.

Separate from mutagenic effects, this type of UV is also implicated in the etiology of cancer via immunosuppression. This immunomodulation results in depletion of the Langerhans cells from the epidermis, improper antigen presentation in the lymph nodes, a shift towards Th2 responses, and development of tumor antigen-specific T regulatory cells, resulting in blocked immune surveillance and tumor outgrowth [4], [5], [6], [7], [8], [9]. Studies using antibody-mediated cytokine suppression and genetically engineered mice have found a wealth of downstream mediators that are critical in UV-induced immune responses.

Strains of inbred mice may be classified into distinct categories of UV-susceptibility and UV-resistance following equal doses of UVR, implicating a genetic component to susceptibility to UV-induced immunosuppression [10]. In New Zealand black (NZB) mice, a strain that exhibits deficiencies in maintaining self-tolerance which lead to a murine form of human systemic lupus erythematosis [11], there was a seven fold increase in sensitivity to UVB in females compared to males, implicating possible gender differences in this process. In both sexes, UV-susceptible mice have higher incidence rates of skin cancer than UV-resistant mice [12]. Preliminary data from two small studies in humans suggest a similar association. An estimated 35–40% of humans may be classified as having a UV-susceptible phenotype, as measured by a contact hypersensitivity test [13], [14]. One of these studies also found that over 90% of skin cancer patients were of the UV-susceptible phenotype [13], further linking cancer development, genetic susceptibility, and UV immunosuppression.

In this study, we analyzed purported functional variants in 10 key mediators of UV-induced immunosuppression and risk of NMSC, including investigation of both single and multiple gene effects. Additionally, we investigated whether these effects varied by gender, as past studies have indicated possible gender differences in risk of NMSC from UV-induced immunosuppression.

Methods

Study Population

Newly diagnosed cases of histologically confirmed BCC and SCC in New Hampshire were identified using an incident survey established through the collaboration of dermatologists, dermatopathologists, and pathology laboratories throughout the state and bordering regions from July 1, 1993 to June 30, 1995 (series 1) and July 1, 1997 to March 30, 2000 (series 2) [2]. The study design of The New Hampshire Health Study has been described previously by Karagas et al. [2]. Briefly, eligibility criteria for cases were as follows: 1) between 25 and 74 years of age, 2) had a listed telephone number, and 3) spoke English. All eligible invasive SCC cases and a ratio of approximately two to one BCC cases in series 1 and one to one ratio in series 2 were selected to take part in the study. The BCC cases were randomly sampled in order to ensure representativeness of age, sex, and anatomic site for all incident BCCs within New Hampshire. Controls aged 25–64 years were identified from the New Hampshire State Department of Transportation files and those aged 65–74 years were obtained from enrollment lists from the Center for Medicaid and Medicare Services. Potential controls were frequency-matched on age and gender to the combined distribution of case groups.

A personal interview was conducted with consenting cases and controls, with about 80% of cases and 72% of controls agreeing to participate. The interviews, usually conducted in the participant's home, covered demographic factors, pigmentation characteristics, sun exposure and sensitivity, and other factors [2]. Blood draws and/or buccal samples were obtained from cases and controls from both phases of the study for DNA analysis. Approximately 85% of subjects consented to a providing a DNA sample; among those that consented, 90% provided a blood-derived sample. All study protocol and materials were approved by the Dartmouth College Committee for the Protection of Human Subjects, and all participants provided informed consent.

Genotyping

Functional polymorphisms in 10 immune-related genes were genotyped (Table 1). DNA was extracted from peripheral blood lymphocytes of consented cases and controls using Qiagen Genomic DNA extraction kits (Valencia, CA). For quality assurance purposes, 10% of blood and buccal samples were used as integrated duplicates, to which researchers were blinded at the time of genotyping. The genotypes of the embedded duplicates were compared afterwards to that of the original samples to calculate the genotyping error rate. All genotype error rates were 5% or less.

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Table 1. Functional polymorphisms in the UV-induced immunosuppression pathway.

https://doi.org/10.1371/journal.pone.0020019.t001

Genotyping for the histidase I439V SNP (rs7297245) was performed by PCR-RFLP analysis. A 333 base pair fragment of exon 16 of the HAL locus was amplified using primers as previously described [26], [27]. Genotyping of four SNPs (rs1800629, rs3212227, rs2243250, rs1805010) was performed on the Taqman allelic discrimination platform (Applied Biosystems, Foster City, CA). Taqman primers, probes, and conditions are available upon request. All other SNPs (rs6311, rs1800689, rs1061622, rs1800896, rs1800871, rs1800872, rs689466, rs1801275) were genotyping by the University of Minnesota Biomedical Genomics Center using the Sequenom platform. Two IL10 SNPs, rs1800871 and rs1800872, were in high linkage disequilibrium (D' = 0.99) in our population, and therefore rs1800872 was not included in the analysis.

Logistic Regression

Adjusted odds ratios (ORs) and 95% confidence intervals for each SNP were obtained using unconditional logistic regression adjusting for age at diagnosis (continuous), gender, skin type and lifetime number of severe sunburns. Self-reported sunburn history was described as the lifetime number of painful sunburns that last 2 or more days. For all analyses, cutoffs were determined based on the distribution in controls, creating groups of no (0), low (1–3), and high (≥4) burns. For stratified analysis, the no and low groups were combined, as done in previous analysis [27]. The measure of skin type, skin's reaction to acute sun exposure, was also trichotomized. Responses were grouped as tan, burn then tan, or burn, if they responded that they burned and peeled or burned and freckled.

Multifactor Dimensionality Reduction

Multifactor dimensionality reduction (MDR) is a nonparametric analysis method in which multiple variables, or attributes, are reduced into a single, binary attribute with “low risk” and “high risk” categories. The specifics of the algorithm used have been previously described [28]. Analysis was conducted for 1 through 5 factor attribute combinations. Ten-fold cross validation was used to develop training and testing sets for each analysis. For those models where the cross validation consistency (CVC) was not 10/10, the true testing balance accuracy (TBA) of that combination was recalculated using only those variables from the most accurate model. This TBA and the original CVC were reported. To determine statistical significance, a normal distribution of testing balance accuracy values was derived by permutating the data 1000 times. As in logistic regression, all genotypes were binary except IL10 and IL4R. Age was dichotomized as 60 and younger or over 60 years. All other variables were coded as described above.

Classification and Regression Trees

Classification and regression trees (CART) is a decision tree-based analysis method that uses binary recursive partitioning to create prediction rules for the outcome of interest. The details of the algorithm used have been previously described [29], [30]. All variables were coded the same as in MDR analysis. A 10-fold cross validation was used for model building, and the optimal tree was chosen as the one with the highest ROC value. To compute the prediction rate, a bootstrap aggregation method was applied to the data, in which 500 trees were averaged to create a “committee of experts” model to best explain the variability in the data.

Results

Evaluation of genetic variants was conducted in 2493 participants (852 controls, 931 BCC, 710 SCC). The frequency distributions for age, sex, and other known risk factors for NMSC, such as skin type and lifetime number of severe sunburns, are shown in Table 2. The average age of participants was 61.3 years (SD = 10.6) for controls, 58.7 years (SD = 11.1) for BCC, and 64.1 years (SD = 8.7) for SCC. In all groups, there were more men than women. BCC and SCC cases were more likely to have experienced severe sunburns and were more likely to burn than controls.

Unconditional logistic regression was used to examine the individual effects of each SNP or haplotype in the pathway. While controlling for age, sex, skin type, and lifetime number of sunburns, IL10 GC haplotypes were associated with increased risk of both BCC (Table 3) and SCC (Table 4). Having two GC haploytypes, which is associated with higher IL10 expression than the AT allele [20], was associated with increased ORs of BCC and SCC (ORBCC = 1.5, 95% CI 1.1–1.9; ORSCC = 1.4, 95% CI 1.0–1.9), although the association with SCC was of borderline significance. There was evidence of a gene dosage effect, with increasing ORs associated with number of GC haplotypes (BCC: ptrend = 0.0048; SCC: ptrend = 0.031). After using the conservative Bonferroni multiple comparisons correction for 10 independent test (p<0.005), the trend in BCC remains significant, but the trend is no longer significant in SCC. When the number of IL10 GC haplotypes was treated as a continuous variable, there was a significant 20% increase in risk of both BCC and SCC associated with each additional GC haplotype (BCC: ORBCC = 1.2, 95% CI 1.1–1.4; SCC: ORSCC = 1.2, 95% CI 1.0–1.4), although again this association was of borderline significance in SCC. As shown in a previous study in this population, there was no significant association between HAL genotype and BCC or SCC [27].

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Table 3. Logistic regression analysis of individual SNPs or haplotypes and BCC.

https://doi.org/10.1371/journal.pone.0020019.t003

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Table 4. Logistic regression analysis of individual SNPs or haplotypes and SCC.

https://doi.org/10.1371/journal.pone.0020019.t004

When stratified by gender, the IL10 association appeared to be largely restricted to women for both histologies. For BCC and SCC, women with 2 IL10 GC haplotypes had an OR of about 2 (ORBCC = 2.2, 95%CI 1.4–3.4; ORSCC = 1.8, 95% CI 1.1–3.0), and these trends were significant (BCC: p = 0.0005; SCC: p = 0.020). Again, after a Bonferroni correction for 20 independent test (10 genes in men and 10 genes in women, p<0.0025), this trend remains significant in BCC in women, but not SCC under this more stringent requirement. Among men, the ORs were close to one (BCC: OR = 1.1, 95% CI 0.8–1.6; SCC: OR = 1.2, 95% CI 0.8–1.7). As previously reported [27], HAL AG/GG was associated with increased risk of SCC in women (Table 4, OR = 1.5, 95% CI 1.0–2.1). Finally, 1–2 variant alleles of the IL4R genes were associated with increased OR of SCC in men (Table 4, OR = 1.5, 95% CI 1.1–2.1) but not women.

MDR analysis for BCC found the most accurate one factor model considers lifetime number of severe sunburns (testing balance accuracy (TBA) = 0.5729, cross validation consistency (CVC) = 10/10, p<0.001), but a 3 factor model including a combination of skin type, burns, and IL4R genotype (TBA = 0.5684, CVC = 9/10, p<0.002) and a 4 factor model adding IL10 haplotypes (TBA = 0.5627, CVC = 8/10, p<0.005) were also statistically significant. The best model of SCC included skin type and sunburns (TBA = 0.5794, CVC = 9/10, p<0.001). A three factor model including IL4R haplotypes (TBA = 0.5718, CVC = 4/10, p<0.001) was also statistically significant but not consistently computed as the best model. Of borderline statistical significance was a four factor model including IL10 and IL4R haplotypes (TBA = 0.5434, CVC = 5/10, p<0.054).

Similar results were found using CART. For BCC, combinations of IL4R and IL10 and IL4 and burns was found among those who tended to either burn or burn then tan and were older than 60 years (Figure 1). For SCC, a combination of IL10, TNFR2, and IL4R were important genetic factors among those with a high lifetime number of sunburns who tend to burn or burn then tan (Figure 2).

When examining these factors in men only, the two analysis methods identified skin type, burns, IL10, IL4R, and to a lesser extent TNFR2 as contributing to risk of BCC. In men, the best models in MDR consider lifetime number of severe sunburns (TBA = 0.5776, CVC = 10/10, p<0.002) and a combination of skin type, burns, and IL10 and IL4R haplotypes (TBA = 0.5764, CVC = 10/10, p = 0.002). Similarly, analysis using CART found IL4R, IL10, and TNFR2 best predicted risk among those who tended to burn or burn then tan and were older than 60 years.

In women only, both analysis methods found combinations of skin type, burns, IL10, HTR2A, IL12B, and IL4R contributed to risk of BCC. The best fit models for MDR included skin type and IL10 (TBA = 0.5908, CVC = 10/10, p<0.008) and skin type, burns and IL10 (TBA = 0.5998, CVC = 10/10, p<0.004). Skin type, burns, IL10, HTR2A, IL12B, and IL4R were related to BCC risk using CART.

As with BCC, the risk of SCC in men identified skin type, burns, IL10, IL4R, and possibly TNFR2 as significant factors. In MDR, the best model involved burns and IL10 and IL4R haplotypes (TBA = 0.5704, CVC = 5/10, p<0.03). Using CART, two risk groups were identified: one with burns, skin type, IL10, and TNFR2, and a second with burns, age, skin type, and IL4R.

Among women, both methods found skin type, burns, and IL10 related to risk of SCC. By MDR, significant models included just skin type (TBA = 0.5863, CVC = 8/10, p<0.05) and skin type, burns, and IL10 haplotypes (TBA = 0.5861, CVC = 8/10, p<0.05). In CART, skin type, burns, IL10 and TNF best explained the variation in the data.

Discussion

We have investigated the effects of multiple functional variants in genes of the UV-induced immunosuppression pathway in non-melanoma skin cancer etiology. We found a main effect for IL10 haplotypes in both BCC and SCC. Stratifying on gender suggested this was primarily attributable to the strong association in women. In men, skin type, burns, IL10, IL4R, and possibly TNFR2 were associated with both BCC and SCC. In women, skin type, burns, and IL10 were related to risk of SCC and BCC, and risk of BCC additionally included HTR2A, IL12B and IL4R.

A prior study had examined the role of IL10 polymorphisms in UV-induced immune suppression. In this phenotype study, a CA-repeat polymorphism in the promoter region was not associated with susceptibility to UV-induced immune suppression [31]. It is possible that the CA repeat does not capture the reduced expression phenotype associated with the 2 SNP haplotype in our study. Additionally, a small population size (N = 42) and the large number of CA repeat alleles could have resulted in a false negative finding. This study also examined the role of TNF -308 and found no association, consistent with our results.

Previous epidemiologic studies have found a similar link between IL10 promoter polymorphisms and risk of NMSCs in immunocompromised populations. Among renal transplant patients, a higher number of GC (or GCC) alleles was found in SCC patients compared to unaffected patients [32], and secreted IL-10 levels were also higher in this group. This was not true for BCC. A study in non-transplant patients examined the association of IL10 -1082 and BCC and also found no association [33]. Therefore, our association between BCC and IL10 appears to be a novel finding that warrants replication in another population.

Other previous work focused on patients with epidermodysplasia verruciformis (EV), a disease characterized by defects in cell-mediated immunity that result in persistent infection with beta-type human papillomavirus (β-HPV) and increased development of non-melanoma skin cancer [34], [35]. EV patients (n = 19) were more likely to have the low expressing (no GCC) alleles than controls (n = 25), and within EV patients, those that developed malignancies (n = 14) were also more likely to have low expressing IL10 alleles. This could indicate a different causal pathway for HPV-related NMSC that is unrelated to UV-induced immunosuppression.

A small study conducted in a Japanese population (32 BCC, 24 SCC, 50 controls) also found an inverse association between number of GC(C) alleles and risk of in situ SCC (Bowen's disease) in non-transplant patients [36], but no association with BCC or SCC. Bowen's disease patients are excluded from our population; therefore, we have no ability to asses this relationship. Previous studies have shown much lower prevalence of these polymorphisms in Japanese populations [37], [38], [39] compared to Caucasians. Thus, aside from the small study size ethnic variation may account for differences in our results. Further, the control group consisted partially of patients with fungal or bacterial infections, which could potentially have been related to a pre-existing immune problem.

MDR and CART analyses identified IL10 and IL4R haplotypes as being related to both BCC and SCC. IL4 has been shown to induce IL10 production in this pathway [40]. Further, IL4R is necessary to up-regulate IL10, a key component in biasing immune reactions towards the Th2 phenotype [41].

We have analyzed the role of gender differences in genetic susceptibility to UV-induced immunosuppression. In addition to the increased susceptibility to UV-induced immunosuppression seen in the female NZB mice, evidence exists for a role of estrogen in regulating wider immune signaling. Experimental evidence supports the fact that estrogen promotes a Th-2 bias, similar to UVR. In pregnancy, when circulating estrogen levels are high, the fetus spontaneously releases Th-2 cytokines (i.e. IL-4 and IL-10), hence biasing the mother's immune system away from producing Th-1 type cytokines which are implicated in spontaneous abortions [42]. Similar to UVR, contraceptive level doses of β-estradiol result in suppression of delayed-type hypersensitivity (DTH) reactions [43]. β-estradiol inhibits the recruitment of inflammatory cells types, such as granulocytes, macrophages, and T cells, to sites of inflammation [44]. Also, T cell activation does not occur, due to improper antigen presentation from spleen antigen presenting cells (APCs) [43], [45]. Considering women may be more primed for immune suppression given the effects of β-estradiol, it is not surprising that our genetic effects were stronger in women.

One advantage of a pathway-based analysis is the ability to examine how combinations of genotypes contribute to disease risk. Often this is done by examining all of the common variants in each gene to guarantee complete coverage of all the variation in the pathway. However, this approach is costly, and the large number of data points and comparisons can increase the chances of type 2 errors. Instead, we have taken a phenotypic approach to pathway analysis, using almost exclusively SNPs that have been reported as functional in past studies (Table 1). While this does not guarantee full coverage of the pathway variation, it has the advantage of improving statistical power and improving interpretability, as the genotypes have an identified phenotype. However, it is important to note that functionality of a SNP does not guarantee that it is the causal SNP, in relation to the outcome of interest; the possibility of the causal SNP being in linkage disequilibrium with the SNP examined still remains.

Major strengths of this study include the population-based nature of the study and the large sample size included, yielding increased generalizability and power to detect smaller genetic effects. Possible limitations include recall bias and missing genetic information for all variants in the population. Sun exposure risk factors of interest in this study were determined by self-reported interview responses, which are subject to recall bias. However, standardized interview instruments like the one used in the NHHS tend to yield reproducible results upon retest for many sun exposure variables [46], [47]. Additionally, there was no evidence of differential recall of sunburns between cases and controls in either study. Finally, use of sunburns as a categorical variable instead of a continuous variable has been shown to improve reproducibility of recall [47].

While genotyping is not complete for any of the genes studied, overall the rate of missing data is relatively small. For 8 of the 10 genes examined, 94% or greater of the 2,493 participants in this study could be assigned a genotype or haplotye. IL12B and IL4R had slightly lower overall genotyping rates, at 90.1% and 87.1%, respectively. However, missing genetic information was not associated with either outcome of interest for any of the genes examined, so we do not believe that this is contributing to a substantial bias in the study.

In this study, we have examined the role of functional polymorphisms in the UV-induced immunosuppression pathway and how they alter risk for NMSC. Like many other cancers, BCC and SCC are both complex diseases where genetic predisposition and environmental exposures, as well and their interactions, contribute enormously to disease etiology. The combinations of gene and environmental (sunburn) effects observed in this study underline the importance of examining genetic variants as part of the greater pathway to which they belong. While the highly antigenic nature of NMSCs make them well-suited to examine the role of genetic variants in the UV-induced immunosuppression pathway, tumor surveillance plays a part in many types of cancers, and thus the interactions found in this study may have applications to a variety of solid tumor types.

Author Contributions

Conceived and designed the experiments: MWW MRK HHN. Performed the experiments: MMW JKK. Analyzed the data: MMW AH HHN. Contributed reagents/materials/analysis tools: MRK SKK AEP. Wrote the paper: MWW MRK HHN.

References

  1. 1. ACS (2005) Cancer Facts and Figures 2005. Atlanta: American Cancer Society. ACS2005Cancer Facts and Figures 2005.AtlantaAmerican Cancer Society
  2. 2. Karagas MR, Greenberg ER, Spencer SK, Stukel TA, Mott LA (1999) Increase in incidence rates of basal cell and squamous cell skin cancer in New Hampshire, USA. New Hampshire Skin Cancer Study Group. Int J Cancer 81: 555–559.MR KaragasER GreenbergSK SpencerTA StukelLA Mott1999Increase in incidence rates of basal cell and squamous cell skin cancer in New Hampshire, USA. New Hampshire Skin Cancer Study Group.Int J Cancer81555559
  3. 3. Karagas MR, Martin A. Weinstock, Heather H. Nelson (2006) Keratinocyte Carcinomas (Basal and Squamous Cell Carcinomas of the Skin). In: Schottenfeld DaJFF, editor. Cancer Epidemiology and Prevention, 3rd ed: Oxford University Press, USA. MR KaragasA. Weinstock MartinH. Nelson Heather2006Keratinocyte Carcinomas (Basal and Squamous Cell Carcinomas of the Skin).DaJFF SchottenfeldCancer Epidemiology and Prevention, 3rd ed: Oxford University Press, USA
  4. 4. Morison WL, Bucana C, Kripke ML (1984) Systemic suppression of contact hypersensitivity by UVB radiation is unrelated to the UVB-induced alterations in the morphology and number of Langerhans cells. Immunology 52: 299–306.WL MorisonC. BucanaML Kripke1984Systemic suppression of contact hypersensitivity by UVB radiation is unrelated to the UVB-induced alterations in the morphology and number of Langerhans cells.Immunology52299306
  5. 5. Noonan FP, Bucana C, Sauder DN, De Fabo EC (1984) Mechanism of systemic immune suppression by UV irradiation in vivo. II. The UV effects on number and morphology of epidermal Langerhans cells and the UV-induced suppression of contact hypersensitivity have different wavelength dependencies. J Immunol 132: 2408–2416.FP NoonanC. BucanaDN SauderEC De Fabo1984Mechanism of systemic immune suppression by UV irradiation in vivo. II. The UV effects on number and morphology of epidermal Langerhans cells and the UV-induced suppression of contact hypersensitivity have different wavelength dependencies.J Immunol13224082416
  6. 6. Cooper KD, Oberhelman L, Hamilton TA, Baadsgaard O, Terhune M, et al. (1992) UV exposure reduces immunization rates and promotes tolerance to epicutaneous antigens in humans: relationship to dose, CD1a-DR+ epidermal macrophage induction, and Langerhans cell depletion. Proc Natl Acad Sci U S A 89: 8497–8501.KD CooperL. OberhelmanTA HamiltonO. BaadsgaardM. Terhune1992UV exposure reduces immunization rates and promotes tolerance to epicutaneous antigens in humans: relationship to dose, CD1a-DR+ epidermal macrophage induction, and Langerhans cell depletion.Proc Natl Acad Sci U S A8984978501
  7. 7. Saijo S, Kodari E, Kripke ML, Strickland FM (1996) UVB irradiation decreases the magnitude of the Th1 response to hapten but does not increase the Th2 response. Photodermatol Photoimmunol Photomed 12: 145–153.S. SaijoE. KodariML KripkeFM Strickland1996UVB irradiation decreases the magnitude of the Th1 response to hapten but does not increase the Th2 response.Photodermatol Photoimmunol Photomed12145153
  8. 8. Ullrich SE, Kripke ML (1984) Mechanisms in the suppression of tumor rejection produced in mice by repeated UV irradiation. J Immunol 133: 2786–2790.SE UllrichML Kripke1984Mechanisms in the suppression of tumor rejection produced in mice by repeated UV irradiation.J Immunol13327862790
  9. 9. Jessup JM, Hanna N, Palaszynski E, Kripke ML (1978) Mechanisms of depressed reactivity to dinitrochlorobenzene and ultraviolet-induced tumors during ultraviolet carcinogenesis in BALB/c mice. Cell Immunol 38: 105–115.JM JessupN. HannaE. PalaszynskiML Kripke1978Mechanisms of depressed reactivity to dinitrochlorobenzene and ultraviolet-induced tumors during ultraviolet carcinogenesis in BALB/c mice.Cell Immunol38105115
  10. 10. Noonan FP, Hoffman HA (1994) Susceptibility to immunosuppression by ultraviolet B radiation in the mouse. Immunogenetics 39: 29–39.FP NoonanHA Hoffman1994Susceptibility to immunosuppression by ultraviolet B radiation in the mouse.Immunogenetics392939
  11. 11. Borchers A, Ansari AA, Hsu T, Kono DH, Gershwin ME (2000) The pathogenesis of autoimmunity in New Zealand mice. Semin Arthritis Rheum 29: 385–399.A. BorchersAA AnsariT. HsuDH KonoME Gershwin2000The pathogenesis of autoimmunity in New Zealand mice.Semin Arthritis Rheum29385399
  12. 12. Noonan FP, Muller HK, Fears TR, Kusewitt DF, Johnson TM, et al. (2003) Mice with genetically determined high susceptibility to ultraviolet (UV)-induced immunosuppression show enhanced UV carcinogenesis. J Invest Dermatol 121: 1175–1181.FP NoonanHK MullerTR FearsDF KusewittTM Johnson2003Mice with genetically determined high susceptibility to ultraviolet (UV)-induced immunosuppression show enhanced UV carcinogenesis.J Invest Dermatol12111751181
  13. 13. Yoshikawa T, Rae V, Bruins-Slot W, Van den Berg JW, Taylor JR, et al. (1990) Susceptibility to effects of UVB radiation on induction of contact hypersensitivity as a risk factor for skin cancer in humans. J Invest Dermatol 95: 530–536.T. YoshikawaV. RaeW. Bruins-SlotJW Van den BergJR Taylor1990Susceptibility to effects of UVB radiation on induction of contact hypersensitivity as a risk factor for skin cancer in humans.J Invest Dermatol95530536
  14. 14. Vermeer M, Schmieder GJ, Yoshikawa T, van den Berg JW, Metzman MS, et al. (1991) Effects of ultraviolet B light on cutaneous immune responses of humans with deeply pigmented skin. J Invest Dermatol 97: 729–734.M. VermeerGJ SchmiederT. YoshikawaJW van den BergMS Metzman1991Effects of ultraviolet B light on cutaneous immune responses of humans with deeply pigmented skin.J Invest Dermatol97729734
  15. 15. Myers RL, Airey DC, Manier DH, Shelton RC, Sanders-Bush E (2007) Polymorphisms in the regulatory region of the human serotonin 5-HT2A receptor gene (HTR2A) influence gene expression. Biol Psychiatry 61: 167–173.RL MyersDC AireyDH ManierRC SheltonE. Sanders-Bush2007Polymorphisms in the regulatory region of the human serotonin 5-HT2A receptor gene (HTR2A) influence gene expression.Biol Psychiatry61167173
  16. 16. Bouma G, Crusius JB, Oudkerk Pool M, Kolkman JJ, von Blomberg BM, et al. (1996) Secretion of tumour necrosis factor alpha and lymphotoxin alpha in relation to polymorphisms in the TNF genes and HLA-DR alleles. Relevance for inflammatory bowel disease. Scand J Immunol 43: 456–463.G. BoumaJB CrusiusM. Oudkerk PoolJJ KolkmanBM von Blomberg1996Secretion of tumour necrosis factor alpha and lymphotoxin alpha in relation to polymorphisms in the TNF genes and HLA-DR alleles. Relevance for inflammatory bowel disease.Scand J Immunol43456463
  17. 17. Braun N, Michel U, Ernst BP, Metzner R, Bitsch A, et al. (1996) Gene polymorphism at position -308 of the tumor-necrosis-factor-alpha (TNF-alpha) in multiple sclerosis and it's influence on the regulation of TNF-alpha production. Neurosci Lett 215: 75–78.N. BraunU. MichelBP ErnstR. MetznerA. Bitsch1996Gene polymorphism at position -308 of the tumor-necrosis-factor-alpha (TNF-alpha) in multiple sclerosis and it's influence on the regulation of TNF-alpha production.Neurosci Lett2157578
  18. 18. Morita C, Horiuchi T, Tsukamoto H, Hatta N, Kikuchi Y, et al. (2001) Association of tumor necrosis factor receptor type II polymorphism 196R with Systemic lupus erythematosus in the Japanese: molecular and functional analysis. Arthritis Rheum 44: 2819–2827.C. MoritaT. HoriuchiH. TsukamotoN. HattaY. Kikuchi2001Association of tumor necrosis factor receptor type II polymorphism 196R with Systemic lupus erythematosus in the Japanese: molecular and functional analysis.Arthritis Rheum4428192827
  19. 19. Seegers D, Zwiers A, Strober W, Pena AS, Bouma G (2002) A TaqI polymorphism in the 3′UTR of the IL-12 p40 gene correlates with increased IL-12 secretion. Genes Immun 3: 419–423.D. SeegersA. ZwiersW. StroberAS PenaG. Bouma2002A TaqI polymorphism in the 3′UTR of the IL-12 p40 gene correlates with increased IL-12 secretion.Genes Immun3419423
  20. 20. Turner DM, Williams DM, Sankaran D, Lazarus M, Sinnott PJ, et al. (1997) An investigation of polymorphism in the interleukin-10 gene promoter. Eur J Immunogenet 24: 1–8.DM TurnerDM WilliamsD. SankaranM. LazarusPJ Sinnott1997An investigation of polymorphism in the interleukin-10 gene promoter.Eur J Immunogenet2418
  21. 21. Zhang X, Miao X, Tan W, Ning B, Liu Z, et al. (2005) Identification of functional genetic variants in cyclooxygenase-2 and their association with risk of esophageal cancer. Gastroenterology 129: 565–576.X. ZhangX. MiaoW. TanB. NingZ. Liu2005Identification of functional genetic variants in cyclooxygenase-2 and their association with risk of esophageal cancer.Gastroenterology129565576
  22. 22. Rosenwasser LJ, Klemm DJ, Dresback JK, Inamura H, Mascali JJ, et al. (1995) Promoter polymorphisms in the chromosome 5 gene cluster in asthma and atopy. Clin Exp Allergy 25 Suppl 2: 74–78.LJ RosenwasserDJ KlemmJK DresbackH. InamuraJJ Mascali1995Promoter polymorphisms in the chromosome 5 gene cluster in asthma and atopy.Clin Exp Allergy 25 Suppl27478discussion 95-76. discussion 95-76.
  23. 23. Mitsuyasu H, Izuhara K, Mao XQ, Gao PS, Arinobu Y, et al. (1998) Ile50Val variant of IL4R alpha upregulates IgE synthesis and associates with atopic asthma. Nat Genet 19: 119–120.H. MitsuyasuK. IzuharaXQ MaoPS GaoY. Arinobu1998Ile50Val variant of IL4R alpha upregulates IgE synthesis and associates with atopic asthma.Nat Genet19119120
  24. 24. Risma KA, Wang N, Andrews RP, Cunningham CM, Ericksen MB, et al. (2002) V75R576 IL-4 receptor alpha is associated with allergic asthma and enhanced IL-4 receptor function. J Immunol 169: 1604–1610.KA RismaN. WangRP AndrewsCM CunninghamMB Ericksen2002V75R576 IL-4 receptor alpha is associated with allergic asthma and enhanced IL-4 receptor function.J Immunol16916041610
  25. 25. Andrews RP, Burrell L, Rosa-Rosa L, Cunningham CM, Brzezinski JL, et al. (2001) Analysis of the Ser786Pro interleukin-4 receptor alpha allelic variant in allergic and nonallergic asthma and its functional consequences. Clin Immunol 100: 298–304.RP AndrewsL. BurrellL. Rosa-RosaCM CunninghamJL Brzezinski2001Analysis of the Ser786Pro interleukin-4 receptor alpha allelic variant in allergic and nonallergic asthma and its functional consequences.Clin Immunol100298304
  26. 26. Suchi M, Sano H, Mizuno H, Wada Y (1995) Molecular cloning and structural characterization of the human histidase gene (HAL). Genomics 29: 98–104.M. SuchiH. SanoH. MizunoY. Wada1995Molecular cloning and structural characterization of the human histidase gene (HAL).Genomics2998104
  27. 27. Welsh MM, Karagas MR, Applebaum KM, Spencer SK, Perry AE, et al. (2008) A role for ultraviolet radiation immunosuppression in non-melanoma skin cancer as evidenced by gene-environment interactions. Carcinogenesis. MM WelshMR KaragasKM ApplebaumSK SpencerAE Perry2008A role for ultraviolet radiation immunosuppression in non-melanoma skin cancer as evidenced by gene-environment interactions.Carcinogenesis
  28. 28. Moore JH, Gilbert JC, Tsai CT, Chiang FT, Holden T, et al. (2006) A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility. J Theor Biol 241: 252–261.JH MooreJC GilbertCT TsaiFT ChiangT. Holden2006A flexible computational framework for detecting, characterizing, and interpreting statistical patterns of epistasis in genetic studies of human disease susceptibility.J Theor Biol241252261
  29. 29. Breiman L, Jerome Friedman, Richard Olsen, Charles Stone (1984) Classification and Regression Trees. Pacific Grove: Wadsworth. L. BreimanFriedman JeromeOlsen RichardStone Charles1984Classification and Regression Trees.Pacific GroveWadsworth
  30. 30. Steinberg DaPC (1997) CART–Classification and Regression Trees. San Diego, CA: Salford Systems. DaPC Steinberg1997CART–Classification and Regression Trees.San Diego, CASalford Systems
  31. 31. Allen MH, Skov L, Barber R, Trembath R, Simon J, et al. (1998) Ultraviolet B induced suppression of induction of contact sensitivity in human skin is not associated with tumour necrosis factor-alpha-308 or interleukin-10 genetic polymorphisms. Br J Dermatol 139: 225–229.MH AllenL. SkovR. BarberR. TrembathJ. Simon1998Ultraviolet B induced suppression of induction of contact sensitivity in human skin is not associated with tumour necrosis factor-alpha-308 or interleukin-10 genetic polymorphisms.Br J Dermatol139225229
  32. 32. Alamartine E, Berthoux P, Mariat C, Cambazard F, Berthoux F (2003) Interleukin-10 promoter polymorphisms and susceptibility to skin squamous cell carcinoma after renal transplantation. J Invest Dermatol 120: 99–103.E. AlamartineP. BerthouxC. MariatF. CambazardF. Berthoux2003Interleukin-10 promoter polymorphisms and susceptibility to skin squamous cell carcinoma after renal transplantation.J Invest Dermatol12099103
  33. 33. Wilkening S, Hemminki K, Rudnai P, Gurzau E, Koppova K, et al. (2006) Case-control study in basal cell carcinoma of the skin: single nucleotide polymorphisms in three interleukin promoters pre-analysed in pooled DNA. Br J Dermatol 155: 1139–1144.S. WilkeningK. HemminkiP. RudnaiE. GurzauK. Koppova2006Case-control study in basal cell carcinoma of the skin: single nucleotide polymorphisms in three interleukin promoters pre-analysed in pooled DNA.Br J Dermatol15511391144
  34. 34. de Oliveira WR, Rady PL, Grady J, Hughes TK, Festa Neto C, et al. (2003) Polymorphisms of the interleukin 10 gene promoter in patients from Brazil with epidermodysplasia verruciformis. J Am Acad Dermatol 49: 639–643.WR de OliveiraPL RadyJ. GradyTK HughesC. Festa Neto2003Polymorphisms of the interleukin 10 gene promoter in patients from Brazil with epidermodysplasia verruciformis.J Am Acad Dermatol49639643
  35. 35. Majewski S, Jablonska S (1995) Epidermodysplasia verruciformis as a model of human papillomavirus-induced genetic cancer of the skin. Arch Dermatol 131: 1312–1318.S. MajewskiS. Jablonska1995Epidermodysplasia verruciformis as a model of human papillomavirus-induced genetic cancer of the skin.Arch Dermatol13113121318
  36. 36. Nagano T, Kunisada M, Yu X, Masaki T, Nishigori C (2008) Involvement of interleukin-10 promoter polymorphisms in nonmelanoma skin cancers-a case study in non-Caucasian skin cancer patients. Photochem Photobiol 84: 63–66.T. NaganoM. KunisadaX. YuT. MasakiC. Nishigori2008Involvement of interleukin-10 promoter polymorphisms in nonmelanoma skin cancers-a case study in non-Caucasian skin cancer patients.Photochem Photobiol846366
  37. 37. Ide A, Kawasaki E, Abiru N, Sun F, Takahashi R, et al. (2002) Genetic association between interleukin-10 gene promoter region polymorphisms and type 1 diabetes age-at-onset. Hum Immunol 63: 690–695.A. IdeE. KawasakiN. AbiruF. SunR. Takahashi2002Genetic association between interleukin-10 gene promoter region polymorphisms and type 1 diabetes age-at-onset.Hum Immunol63690695
  38. 38. Miyazoe S, Hamasaki K, Nakata K, Kajiya Y, Kitajima K, et al. (2002) Influence of interleukin-10 gene promoter polymorphisms on disease progression in patients chronically infected with hepatitis B virus. Am J Gastroenterol 97: 2086–2092.S. MiyazoeK. HamasakiK. NakataY. KajiyaK. Kitajima2002Influence of interleukin-10 gene promoter polymorphisms on disease progression in patients chronically infected with hepatitis B virus.Am J Gastroenterol9720862092
  39. 39. Origuchi T, Kawasaki E, Ide A, Kamachi M, Tanaka F, et al. (2003) Correlation between interleukin 10 gene promoter region polymorphisms and clinical manifestations in Japanese patients with Sjogren's syndrome. Ann Rheum Dis 62: 1117–1118.T. OriguchiE. KawasakiA. IdeM. KamachiF. Tanaka2003Correlation between interleukin 10 gene promoter region polymorphisms and clinical manifestations in Japanese patients with Sjogren's syndrome.Ann Rheum Dis6211171118
  40. 40. Shreedhar V, Giese T, Sung VW, Ullrich SE (1998) A cytokine cascade including prostaglandin E2, IL-4, and IL-10 is responsible for UV-induced systemic immune suppression. J Immunol 160: 3783–3789.V. ShreedharT. GieseVW SungSE Ullrich1998A cytokine cascade including prostaglandin E2, IL-4, and IL-10 is responsible for UV-induced systemic immune suppression.J Immunol16037833789
  41. 41. Balic A, Harcus YM, Taylor MD, Brombacher F, Maizels RM (2006) IL-4R signaling is required to induce IL-10 for the establishment of T(h)2 dominance. Int Immunol 18: 1421–1431.A. BalicYM HarcusMD TaylorF. BrombacherRM Maizels2006IL-4R signaling is required to induce IL-10 for the establishment of T(h)2 dominance.Int Immunol1814211431
  42. 42. Wegmann TG, Lin H, Guilbert L, Mosmann TR (1993) Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon? Immunol Today 14: 353–356.TG WegmannH. LinL. GuilbertTR Mosmann1993Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon?Immunol Today14353356
  43. 43. Salem ML, Matsuzaki G, Kishihara K, Madkour GA, Nomoto K (2000) beta-estradiol suppresses T cell-mediated delayed-type hypersensitivity through suppression of antigen-presenting cell function and Th1 induction. Int Arch Allergy Immunol 121: 161–169.ML SalemG. MatsuzakiK. KishiharaGA MadkourK. Nomoto2000beta-estradiol suppresses T cell-mediated delayed-type hypersensitivity through suppression of antigen-presenting cell function and Th1 induction.Int Arch Allergy Immunol121161169
  44. 44. Salem ML, Hossain MS, Nomoto K (2000) Mediation of the immunomodulatory effect of beta-estradiol on inflammatory responses by inhibition of recruitment and activation of inflammatory cells and their gene expression of TNF-alpha and IFN-gamma. Int Arch Allergy Immunol 121: 235–245.ML SalemMS HossainK. Nomoto2000Mediation of the immunomodulatory effect of beta-estradiol on inflammatory responses by inhibition of recruitment and activation of inflammatory cells and their gene expression of TNF-alpha and IFN-gamma.Int Arch Allergy Immunol121235245
  45. 45. Matsushima GK, Gilmore W, Casteel N, Frelinger JA, Stohlman SA (1989) Evidence for a subpopulation of antigen-presenting cells specific for the induction of the delayed-type hypersensitivity response. Cell Immunol 119: 171–181.GK MatsushimaW. GilmoreN. CasteelJA FrelingerSA Stohlman1989Evidence for a subpopulation of antigen-presenting cells specific for the induction of the delayed-type hypersensitivity response.Cell Immunol119171181
  46. 46. English DR, Armstrong BK, Kricker A (1998) Reproducibility of reported measurements of sun exposure in a case-control study. Cancer Epidemiol Biomarkers Prev 7: 857–863.DR EnglishBK ArmstrongA. Kricker1998Reproducibility of reported measurements of sun exposure in a case-control study.Cancer Epidemiol Biomarkers Prev7857863
  47. 47. Rosso S, Minarro R, Schraub S, Tumino R, Franceschi S, et al. (2002) Reproducibility of skin characteristic measurements and reported sun exposure history. Int J Epidemiol 31: 439–446.S. RossoR. MinarroS. SchraubR. TuminoS. Franceschi2002Reproducibility of skin characteristic measurements and reported sun exposure history.Int J Epidemiol31439446