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Effects of NFKB1 and NFKBIA Gene Polymorphisms on Susceptibility to Environmental Factors and the Clinicopathologic Development of Oral Cancer

  • Chiao-Wen Lin,

    Affiliations Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan, Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan

  • Yih-Shou Hsieh,

    Affiliations Institute of Biochemistry and Biotechnology, Chung Shan Medical University, Taichung, Taiwan, Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan

  • Chung-Han Hsin,

    Affiliations School of Medicine, Chung Shan Medical University, Taichung, Taiwan, Department of Otolaryngology, Chung Shan Medical University Hospital, Taichung, Taiwan

  • Chun-Wen Su,

    Affiliation Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan

  • Chien-Huang Lin,

    Affiliation Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan

  • Lin-Hung Wei,

    Affiliation Department of Oncology, National Taiwan University Hospital, Taipei, Taiwan

  • Shun-Fa Yang,

    Affiliations Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan, Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan

  • Ming-Hsien Chien

    mhchien1976@gmail.com

    Affiliations Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan, Graduate Institute of Clinical Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

Effects of NFKB1 and NFKBIA Gene Polymorphisms on Susceptibility to Environmental Factors and the Clinicopathologic Development of Oral Cancer

  • Chiao-Wen Lin, 
  • Yih-Shou Hsieh, 
  • Chung-Han Hsin, 
  • Chun-Wen Su, 
  • Chien-Huang Lin, 
  • Lin-Hung Wei, 
  • Shun-Fa Yang, 
  • Ming-Hsien Chien
PLOS
x

Abstract

Background

Oral cancer, which is the fourth most common cancer in Taiwanese men, is associated with environmental carcinogens. The possibility that genetic predisposition in nuclear factor-kappa B (NF-κB)-signaling pathways activation is linked to the development of oral squamous cell carcinoma (OSCC) requires investigation. The current study examines associations between polymorphisms within promoter regions of NFKB1 encoding NF-κB1 and NFKBIA encoding IkappaBalpha (IκBα) with both the susceptibility to develop OSCC and the clinicopathological characteristics of the tumors.

Methodology/Principal Findings

Genetic polymorphisms of NFKB1 and NFKBIA were analyzed by a real-time polymerase chain reaction (real-time PCR) for 462 patients with oral cancer and 520 non-cancer controls. We found that NFKB1 −94 ATGG1/ATGG2, −94 ATGG2/ATGG2, and the combination of −94 ATGG1/ATGG2 and ATGG2/ATGG2 genotypes NFKBIA −826 T (CT+TT) and −881 G (AG+GG) allelic carriages, were more prevalent in OSCC patients than in non-cancer participants. Moreover, we found that NFKB1 or NFKBIA gene polymorphisms seem to be related to susceptibility to develop oral cancer linked to betel nut and tobacco consumption. Finally, patients with oral cancer who had at least one −519 T allele of the NFKBIA gene were at higher risk for developing distant metastasis (P<.05), compared with those patients CC homozygotes.

Conclusions

Our results suggest that NFKB1 −94 ATTG2, NFKBIA −826 T, and −881 G alleles are associated with oral carcinogenesis. The combination of NFKB1 or NFKBIA gene polymorphisms and environmental carcinogens appears related to an increased risk of oral cancer. More importantly, the genetic polymorphism of NFKBIA −519 might be a predictive factor for the distal metastasis of OSCC in Taiwanese.

Introduction

Oral squamous cell carcinoma (OSCC), a common malignant cancer of the head and neck region, is the fourth most common cancer among men and the sixth leading cause of cancer deaths in Taiwan [1]. OSCC development is a multistep process requiring the accumulation of multiple genetic alterations, influenced by a patient's genetic predisposition and by environmental factors. The environmental factors include alcohol and tobacco consumption, betel (areca) quid chewing, chronic inflammation, and viral infection [1][6]. Gene expression is affected by a single-nucleotide polymorphism (SNP) located within the promoter or other regulatory regions of the gene and are thought to be associated with the development of certain diseases [7]. To elucidate the complex process of carcinogenesis and improve the scientific basis for preventive interventions, the identification of major genes influencing a patient's susceptibility to OSCC should be prioritized.

Activation of nuclear factor-kappa B (NF-κB), a hallmark of the inflammatory response, is detected frequently in tumors and may play an important role in linking inflammation to tumor development and progression [8], [9]. NF-κB was originally identified as a nuclear factor specific to B cells bound to the B site of the κ-light chain gene enhancer. NF-κB is a heterodimer in the Rel family, which contains 5 members: RelA, RelB, c-Rel, p50/105 (NF-κB1), and p52/p100; the dimeric form of NF-κB p50/RelA is the most common form. NF-κB plays a central role in coordinating the expression of a wide variety of genes that control innate and adaptive immune responses, and also plays a critical role in cancer development and progression [8]. In normal cells, NF-κB is inactivated in the cytoplasm by binding to its inhibitor IκB. When IκB proteins are phosphorylated and degraded, NF-κB is released and further translocated to the nucleus, where gene transcription is initiated [10].

The IκB family includes IkappaB alpha (IκBα), IκBβ, IκBγ, IκBδ, IκBε, IκB-ζ, IκB-R, Bcl-3, p100, and p105, which are all constitutively expressed except for IκBα, which is inducibly expressed. IκBα is a classic form of the IκB family that can be found in the cytoplasm and nuclei [11]. Previous studies demonstrated that NF-κB suppression in cancer inhibits cell proliferation, causes cell-cycle arrest, and results in apoptosis, suggesting that NF-κB plays an important role in cell proliferation and survival [12]. Furthermore, NF-κB is known to prevent apoptosis by inducing antiapoptotic proteins, and suppresses the apoptotic potential of chemotherapeutic agents, leading to chemoresistance [13]. Aberrant expression of NF-κB proteins has been well documented in several types of cancer, including OSCC [14], with the level increasing gradually from premalignant lesions to invasive cancer [15]. Moreover, NF-κB1, which comprises p50 homodimers, transcriptionally regulates the antiapoptotic protein Bcl-2, which is overexpressed in a high proportion of oral cancer cases [16]. These various findings suggest that NF-κB signaling plays an important role in oral carcinogenesis.

Prior research has reported that polymorphic variations in promoter regions of the NF-κB1 gene NFKB1 and the IκBα gene NFKBIA and in the 3′-untranslated region (3′-UTR) of NFKBIA were associated with a risk for Hodgkin's lymphoma, multiple myeloma, breast cancer, prostate cancer, gastric cancer, colorectal cancer, and melanoma [17][23]. In Taiwan Lin et al. investigated the −94 ins/del ATTG polymorphism in the NFKB1 promoter among 3 population groups, namely, OSCC patients, male areca chewers with oral submucous fibrosis, and controls (non-areca chewers). They found no significant difference in NFKB1 genotypes among the 3 groups [24]. However, after stratification by age, OSCC was shown to have a higher frequency of the insertion allelotype in patients older than 50 years. No significant difference was found for the NFKB1 allelotype or genotype in patients with OSCC who exhibited different statuses of lymph node metastasis or clinical stage. Apart from the Lin et al. study, no reports have focused on the association between NFKB1 and NFKBIA polymorphisms and OSCC development.

The current study investigated relationships between SNPs in the promoter regions of the NFKB1 and NFKBIA genes and the risk of oral cancer. In addition, we evaluated the influences of these SNPs combined with betel nut and tobacco consumption, which lead to the susceptibility of oral cancer. We also investigated the relationship among genetic influences, environmental exposure, and the clinicopathological characteristics of oral cancer. To our knowledge, this is the first study to demonstrate a significant association between NFKB1 and NFKBIA polymorphisms and oral carcinogenesis.

Materials and Methods

Subjects and specimen collection

We recruited 462 patients (444 men and 18 women, with a mean age of 54.4±11.4 years) at Chung Shan Medical University Hospital in Taichung and Changhua Christian Hospital and Show Chwan Memorial Hospital in Changhua, Taiwan. Patients were enrolled as a case group between 2007 and 2011. For the control group, we randomly chose 520 non-cancer people (426 men and 94 women, with a mean age of 52.4±14.7 years) who visited the same hospitals and resided in the same geographic area. Before commencement of the study, approval was obtained from the Institutional Review Board of Show Chwan Memorial Hospital, and each person provided written informed consent to participate in the study.

For both cases and controls, we used a questionnaire to obtain information on patient exposure to betel quid chewing, tobacco use, and alcohol consumption. Medical information for the cases was obtained from their medical records, and included TMN clinical staging, primary tumor size, lymph node involvement, and histologic grade. Oral cancer patients were clinically staged at the time of diagnosis according to the TNM staging system of the American Joint Committee on Cancer (AJCC) Staging Manual (7th ed.) [25]. Tumor differentiation was examined by a pathologist according to the AJCC classification. Whole blood specimens collected from controls and OSCC patients were placed in tubes containing ethylenediaminetetraacetic acid (EDTA), and were immediately centrifuged and stored at −80°C.

Genomic DNA Extraction

Genomic DNA was extracted using QIAamp DNA blood mini kits (Qiagen, Valencia, CA, USA) following the manufacturer's instructions. We dissolved DNA in a TE buffer (10 mM Tris, 1 mM EDTA; pH 7.8), which was subsequently quantified by measuring the OD260. The final preparation was stored at −20°C and used to create templates for the polymerase chain reaction (PCR).

Real-time PCR

The allelic discrimination of the NFKB1 −94 ATTG, NFKBIA −519, NFKBIA −826, and NFKBIA −881 gene polymorphisms were assessed with the ABI StepOne™ Real-Time PCR System (Applied Biosystems) and analyzed with SDS v3.0 software (Applied Biosystems) using the TaqMan assay. The final volume for each reaction was 5 µL, containing 2.5 µL TaqMan Genotyping Master Mix, 0.125 µL TaqMan probes mix, and 10 ng genomic DNA. The real-time PCR included an initial denaturation step at 95°C for 10 min, followed by 40 cycles at of 95°C for 15 s and then at 60°C for 1 min.

Statistical analysis

Differences between the 2 groups were considered significant if p-values were less than .05. Hardy-Weinberg equilibrium (HWE) was assessed using a goodness-of-fit X2-test for biallelic markers. The Mann-Whitney U-test and Fisher's exact test were used to compare differences in the distributions of patient demographic characteristics between the non-cancer (control) and oral cancer groups. The adjusted odds ratios (ORs) and 95% confidence intervals (CIs) of the association between genotype frequencies and risk in addition to clinicopathological characteristics were estimated using multiple logistic regression models, after controlling for other covariates. We analyzed all data using the Statistical Analytic System (SAS Institute, Cary, NC, USA) software (v. 9.1, 2005) for Windows.

Results

The statistical analysis of demographic characteristics is shown in Table 1. We found significantly different distributions of age (p = 0.023), sex (p<0.001), betel quid chewing (p<0.001), alcohol consumption (p<0.001), and tobacco use (p<0.001) between control participants and OSCC patients. To reduce the possible interference of environmental factors, the adjusted ORs (AORs) with 95% CIs were estimated by multiple logistic regression models after controlling for other covariates in each comparison.

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Table 1. Distributions of demographic characteristics in 520 controls and 462 patients with oral cancer.

https://doi.org/10.1371/journal.pone.0035078.t001

For the control group, all analyzed gene markers were in HWE (p>0.05). The data in Table 2 show that, for both OSCC patients and the controls, alleles with the highest distribution frequency were as follows: heterozygous ATGG1/ATGG2 for the −94 locus of the NFKB1 gene; and homozygous C/C, C/C, and AA, respectively, for −519, −826, and −881 loci of the NFKBIA gene. According to the AORs (95% CI), significantly (p<0.05) higher risks for OSCC were noted for NFKB1 gene polymorphisms −94 ATGG1/ATGG2,−94 ATGG2/ATGG2, and the combination of −94 ATGG1/ATGG2 and ATGG2/ATGG2 genotypes. Compared with the corresponding wild-type (WT) homozygotes of the control group, the risk for OSCC was 1.8-fold (95% CI = 1.2∼2.8) for −94 ATGG1/ATGG2; 2.2-fold (95% CI = 1.2–4.2) for −94 ATGG2/ATGG2l; and 1.8-fold (95% CI = 1.2–2.8) for the combination of −94 ATGG1/ATGG2 and ATGG2/ATGG2. These results were obtained after adjusting for age, sex, betel quid chewing, alcohol consumption, and tobacco use.

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Table 2. Distribution frequencies for NFKB and NFKBIA genotypes in 520 controls and 462 oral cancer patients.

https://doi.org/10.1371/journal.pone.0035078.t002

We also compared the results from participants with the polymorphic gene to those from participants showing the WT gene. We found significantly higher risks for OSCC in participants with the NFKBIA −826 C/T, −826 C/T+T/T, −881 A/G, and −881 A/G+GG polymorphic genotypes. These risks were, respectively, 1.6-fold (95% CI = 1.0–2.6), 1.7-fold (95% CI = 1.1–2.7), 1.6-fold (95% CI = 1.0–2.6), and 1.7-fold (95% CI = 1.2–2.7), compared with the WT. However, people with the NFKBIA −519 polymorphic gene were not at a significantly higher risk than those with the WT gene.

Interactive effects between environmental risk factors and genetic polymorphisms of NFKB1 and NFKBIA are shown in Tables 3 and 4. Among 598 smokers, participants with at least one ATGG2 allele of NFKB1 −94, the T allele of either NFKBIA −519 or 826, or the G allele of NFKBIA −881 were at a higher risk for OSCC if they also chewed betel nut. These increased risks were 67.3-fold (95% CI = 18.9–239.4), 29.5-fold (95% CI = 9.6–91.1), 45.0-fold (95% CI = 14.6–138.5), and 45.0-fold (95% CI = 14.6–138.5), respectively. Similarly, compared with people who had WT homozygotes but did not chew betel nut, people who chewed betel nut and had any one of these polymorphisms were at higher risk for OSCC development. These increased risks were as follows: 6.9-fold (95% CI = 2.5–18.9) for the ATGG2 allele of NFKB1 −94; 14.2-fold (95% CI = 8.3–24.5) for the T allele of NFKBIA −519; 12.4-fold (95% CI = 7.3–21.2) for the T allele of NFKBIA −826; and 12.4-fold (95% CI = 7.3–21.2) for the G allele of NFKBIA −881 (Table 3).

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Table 3. Adjusted odds ratio (AOR) and 95% CI for oral cancer associated with NFKB and NFKBIA genotypic frequencies and betel nut chewing among 598 smokers.

https://doi.org/10.1371/journal.pone.0035078.t003

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Table 4. Adjusted odds ratio (AOR) and 95% CI for oral cancer associated with NFKB and NFKBIA genotypic frequencies and cigarette smoking among 444 betel nut consumers.

https://doi.org/10.1371/journal.pone.0035078.t004

Among betel nut consumers in the cohort, tobacco smoking elevated oral cancer risk significantly in participants polymorphic for NFKB1 in the 94 locus or NFKBIA in three loci (519, 826, and 881), compared with people with the WT gene who did not smoke tobacco (Table 4). Moreover, people who were either polymorphic for NFKBIA in 3 loci (519, 826, and 881) or who smoked were at 4.67- to 5.91-fold risk (p<0.05) of developing oral cancer, compared with people with the WT gene who did not smoke (Table 4). These results suggest that NFKB1 and NFKBIA gene polymorphisms exert a strong influence on oral cancer susceptibility in men who chew betel nut and/or smoke tobacco.

To explore the effects of polymorphic genotypes of NFKB1 and NFKBIA on the clinical status of OSCC, we classified OSCC patients into 2 subgroups. In the first subgroup, patients had homozygous WT alleles, and in the second subgroup, they had at least one polymorphic allele. For the genotypic frequencies of the SNPs, only NFKBIA −519 showed a significant association with clinical pathological variables in OSCC patients. Compared with the WT genotype (C/C), patients with at least one polymorphic T allele of NFKBIA −519 showed a higher risk (4.88-fold; 95% CI = 1.2–20.4) for distant metastasis (Table 5).

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Table 5. Distribution frequencies for clinical status and NFKBIA−519 genotype in 462 patients with OSCC.

https://doi.org/10.1371/journal.pone.0035078.t005

Discussion

The NF-κB pathway plays an important role in tumor development and aggressiveness by enhancing tumor angiogenesis, antiapoptosis, and proliferation, and by repressing the immune response [12], [26]. NF-κB is rarely found to be constitutively active in normal cells, but it is constitutively active in most tumor cell lines [27][29]. Prior research has demonstrated that NF-κB is constitutively activated in OSCC [15]. Furthermore, the −94 insertion/deletion ATTG polymorphism was shown to have a regulatory influence on NFKB1 gene expression; the promoter sequence containing the ATTG2 allele displayed a 2× higher activity than comparable sequences containing the ATTG1 allele [30]. The allele plays an important role in susceptibility to prostate cancer, cervical squamous cell carcinoma, gastric cancer, and hepatocellular carcinoma [22], [23], [31], [32]. Thus, increased risk for oral cancer associated with the NFKB1 ATGG1/ATGG2 variant might have resulted from its positive regulation of NF-κB expression (Table 2).

Alcohol consumption, tobacco smoking, and betel quid chewing are the main known etiologic factors of oral cancer. In this study, we observed that higher ratios of people in the OSCC group had consumed alcohol and tobacco and chewed betel quid (61.7%, 84.0%, and 76.4%, respectively), compared with the controls (40.3%, 40.4%, and 17.5%, respectively) (Table 1). This finding indicated that alcohol and tobacco consumption and betel quid chewing are highly associated with increased risks for oral cancer. Long-term tobacco smoking and betel nut chewing have been shown to contribute to carcinogenesis [3][5], [33]. Betel nut constituents can increase protein levels of c-fos and c-jun proto-oncogenes, and tobacco consumption can significantly increase nuclear hypoxia-inducible factor (HIF)-1α expression in oral cancer [34], [35].

People carrying the murine double minute 2 (MDM2) SNP 309 GG genotype have oral mucosa that is more susceptible to environmental carcinogens, including tobacco, alcohol, and betel nuts [36]. Therefore, exposure to these factors can result in earlier onset of tumor formation [36]. Accordingly, we evaluated the combined effect of environmental carcinogens and NFKB1 gene polymorphisms on the risk of oral cancer (Tables 2, 3). We found that the NFKB1 −94 insertion/deletion ATTG polymorphism combined with betel quid chewing and smoking further increased risk of oral carcinogenesis. This phenomenon might be caused by alterations in the binding affinities between betel nut and tobacco constituents and the promoter of the polymorphic NFKB1 gene. Consequently, expression or activity of NF-κB was further changed. Several earlier reports have indicated that tobacco and betel nut constituents can induce NF-κB activation in oral keratinocytes [37], [38]. Moreover, evidence has shown that alkaline saliva generated by chewing betel quid may play a role in cigarette-related nicotine-induced DNA damage, and reactive oxygen species may be involved in generating this DNA damage [39]. These findings provide a possible molecular explanation for the synergistic effect of betel quid chewing and smoking in oral cancer development. However, details underlying the mechanism must be verified by other well-designed experiments.

An imbalance between NF-κB and IκB is a critical step in tumor development and response to treatment [40]. Polymorphisms of the 3 loci (519, 826, and 881) of the NFKBIA promoter were investigated in this study. The −881 position was selected based on potential functional effects because of its location within the transcription factor, retinoic acid-related orphan receptor α (RORα), and binding sites [41]. NFKBIA −881G might alter the binding ability of RORα, which plays a potential role in cancer development [41]. Moreover, 881 and −826 in the NFKBIA promoter showed strong local linkage disequilibrium (LD) in 2 Asian populations (Chinese and Japanese). The current study findings showed that Taiwanese men with at least one polymorphic G allele of NFKBIA −881 or the T allele of NFKBIA −826 are at a high risk for oral carcinogenesis (Table 2). The synergistic effect of environmental factors (betel quid and smoking) and NFKBIA −881 and −826 polymorphisms on the risk of oral cancer was also demonstrated adequately (Tables 3 and 4).

Although to date no direct evidence has been presented proving that −881G or −826T at the promoter of NFKBIA decreases promoter activity, indirect evidence indicates this possibility. For instance, NF-κB expression was twice as high in patients with sarcoidosis, compared with that of control participants. In contrast, the −881G and −826T allelic carriages were more prevalent in sarcoidosis patients than in controls [42], indicating that the −881G and −826T allelic carriages might be associated with increased activity of NF-κB. Because IκBα is an absolute requirement for normal termination of the NF-κB response [11], NFKBIA −881G and −826T allelic carriages were thought to retard efficient IκBα expression.

In conclusion, our results suggest that NFKB1 gene polymorphisms might be correlated with oral cancer susceptibility, and the combined effect of NFKB1 or NFKBIA gene polymorphisms with environmental carcinogens increases risk of oral cancer development significantly. Patients with oral cancer carrying at least one T allele of NFKBIA −519 are at higher risk of developing distal metastasis, compared with patients carrying C/C homozygotes.

Author Contributions

Conceived and designed the experiments: CWL MHC. Performed the experiments: YSH CWS. Analyzed the data: CHL CHH LHW. Contributed reagents/materials/analysis tools: MHC SFY. Wrote the paper: MHC.

References

  1. 1. Chung TT, Pan MS, Kuo CL, Wong RH, Lin CW, et al. (2011) Impact of RECK gene polymorphisms and environmental factors on oral cancer susceptibility and clinicopathologic characteristics in Taiwan. Carcinogenesis 32: 1063–8.
  2. 2. Califano J, van der Riet P, Westra W, Nawroz H, Clayman G, et al. (1996) Genetic progression model for head and neck cancer: implications for field cancerization. Cancer Res 56: 2488–92.
  3. 3. Biolchini F, Pollastri G, Figurelli S, Chiarini L (2005) Carcinogen metabolism, DNA damage repair and oral head and neck squamocellular carcinoma (HNSCC). A review. Minerva Stomatol 54: 405–14.
  4. 4. Nagaraj NS, Beckers S, Mensah JK, Waigel S, Vigneswaran N, et al. (2006) Cigarette smoke condensate induces cytochromes P450 and aldo-keto reductases in oral cancer cells. Toxicol Lett 165: 182–94.
  5. 5. Yen CY, Liu SY, Chen CH, Tseng HF, Chuang LY, et al. (2008) Combinational polymorphisms of four DNA repair genes XRCC1, XRCC2, XRCC3, and XRCC4 and their association with oral cancer in Taiwan. J Oral Pathol Med 37: 271–7.
  6. 6. Vairaktaris E, Yapijakis C, Serefoglou Z, Derka S, Vassiliou S, et al. (2007) The interleukin-8 (−251A/T) polymorphism is associated with increased risk for oral squamous cell carcinoma. Eur J Surg Oncol 33: 504–7.
  7. 7. Shastry BS (2002) SNP alleles in human disease and evolution. J Hum Genet 47: 561–6.
  8. 8. Karin M, Greten FR (2005) NF-kappaB: linking inflammation and immunity to cancer development and progression. Nat Rev Immunol 5: 749–59.
  9. 9. Pikarsky E, Porat RM, Stein I, Abramovitch R, Amit S, et al. (2004) NF-kappaB functions as a tumour promoter in inflammation-associated cancer. Nature 431: 461–6.
  10. 10. Gilmore TD (2003) The Re1/NF-kappa B/I kappa B signal transduction pathway and cancer. Cancer Treat Res 115: 241–65.
  11. 11. Whiteside ST, Israel A (1997) I kappa B proteins: structure, function and regulation. Semin Cancer Biol 8: 75–82.
  12. 12. Bharti AC, Aggarwal BB (2002) Nuclear factor-kappa B and cancer: its role in prevention and therapy. Biochem Pharmacol 64: 883–8.
  13. 13. Nakanishi C, Toi M (2005) Nuclear factor-kappaB inhibitors as sensitizers to anticancer drugs. Nat Rev Cancer 5: 297–309.
  14. 14. Dolcet X, Llobet D, Pallares J, Matias-Guiu X (2005) NF-kB in development and progression of human cancer. Virchows Arch 446: 475–82.
  15. 15. Mishra A, Bharti AC, Varghese P, Saluja D, Das BC (2006) Differential expression and activation of NF-kappaB family proteins during oral carcinogenesis: Role of high risk human papillomavirus infection. Int J Cancer 119: 2840–50.
  16. 16. Jordan RC, Catzavelos GC, Barrett AW, Speight PM (1996) Differential expression of bcl-2 and bax in squamous cell carcinomas of the oral cavity. Eur J Cancer B Oral Oncol 32B: 394–400.
  17. 17. Chang ET, Birmann BM, Kasperzyk JL, Conti DV, Kraft P, et al. (2009) Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma. Cancer Epidemiol Biomarkers Prev 18: 976–86.
  18. 18. Spink CF, Gray LC, Davies FE, Morgan GJ, Bidwell JL (2007) Haplotypic structure across the I kappa B alpha gene (NFKBIA) and association with multiple myeloma. Cancer Lett 246: 92–9.
  19. 19. Bu H, Rosdahl I, Sun XF, Zhang H (2007) Importance of polymorphisms in NF-kappaB1 and NF-kappaBIalpha genes for melanoma risk, clinicopathological features and tumor progression in Swedish melanoma patients. J Cancer Res Clin Oncol 133: 859–66.
  20. 20. Curran JE, Weinstein SR, Griffiths LR (2002) Polymorphic variants of NFKB1 and its inhibitory protein NFKBIA, and their involvement in sporadic breast cancer. Cancer Lett 188: 103–7.
  21. 21. Gao J, Pfeifer D, He LJ, Qiao F, Zhang Z, et al. (2007) Association of NFKBIA polymorphism with colorectal cancer risk and prognosis in Swedish and Chinese populations. Scand J Gastroenterol 42: 345–50.
  22. 22. Lo SS, Chen JH, Wu CW, Lui WY (2009) Functional polymorphism of NFKB1 promoter may correlate to the susceptibility of gastric cancer in aged patients. Surgery 145: 280–5.
  23. 23. Zhang P, Wei Q, Li X, Wang K, Zeng H, et al. (2009) A functional insertion/deletion polymorphism in the promoter region of the NFKB1 gene increases susceptibility for prostate cancer. Cancer Genet Cytogenet 191: 73–7.
  24. 24. Lin SC, Liu CJ, Yeh WI, Lui MT, Chang KW, et al. (2006) Functional polymorphism in NFKB1 promoter is related to the risks of oral squamous cell carcinoma occurring on older male areca (betel) chewers. Cancer Lett 243: 47–54.
  25. 25. Edge SB, Byrd DR, Compton CC, Fritz AG, Greene FL, Trotti A (2010) AJCC cancer staging manual (7th ed). New York, NY: Springer. pp. 111–122.
  26. 26. Yang J, Pan WH, Clawson GA, Richmond A (2007) Systemic targeting inhibitor of kappaB kinase inhibits melanoma tumor growth. Cancer Res 67: 3127–34.
  27. 27. Aggarwal BB (2004) Nuclear factor-kappaB: the enemy within. Cancer Cell 2004;6: 203–8.
  28. 28. Pacifico F, Leonardi A (2006) NF-kappaB in solid tumors. Biochem Pharmacol 2006;72: 1142–52.
  29. 29. Sun XF, Zhang H (2007) NFKB and NFKBI polymorphisms in relation to susceptibility of tumour and other diseases. Histol Histopathol 22: 1387–98.
  30. 30. Karban AS, Okazaki T, Panhuysen CI, Gallegos T, Potter JJ, et al. (2004) Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis. Hum Mol Genet 13: 35–45.
  31. 31. Zhou B, Qie M, Wang Y, Yan L, Zhang Z, et al. (2010) Relationship between NFKB1 −94 insertion/deletion ATTG polymorphism and susceptibility of cervical squamous cell carcinoma risk. Ann Oncol 21: 506–11.
  32. 32. He Y, Zhang H, Yin J, Xie J, Tan X, et al. (2009) IkappaBalpha gene promoter polymorphisms are associated with hepatocarcinogenesis in patients infected with hepatitis B virus genotype C. Carcinogenesis 30: 1916–22.
  33. 33. Lai KC, Lee TC (2006) Genetic damage in cultured human keratinocytes stressed by long-term exposure to areca nut extracts. Mutat Res 599: 66–75.
  34. 34. Lin MH, Wang CJ, Huang HP, Chou MY, Chou FP (2004) The tumorigenic characteristics of lime-piper betel quid-transformed JB6 cells. Arch Toxicol 78: 167–73.
  35. 35. Lin PY, Yu CH, Wang JT, Chen HH, Cheng SJ, et al. (2008) Expression of hypoxia-inducible factor-1 alpha is significantly associated with the progression and prognosis of oral squamous cell carcinomas in Taiwan. J Oral Pathol Med 37: 18–25.
  36. 36. Huang SF, Chen IH, Liao CT, Wang HM, Liou SH, et al. (2009) Combined effects of MDM2 SNP 309 and p53 mutation on oral squamous cell carcinomas associated with areca quid chewing. Oral Oncol 45: 16–22.
  37. 37. Lin SC, Lu SY, Lee SY, Lin CY, Chen CH, et al. (2005) Areca (betel) nut extract activates mitogen-activated protein kinases and NF-kappaB in oral keratinocytes. Int J Cancer 116: 526–35.
  38. 38. Nakao S, Ogata Y, Sugiya H (2009) Nicotine stimulates the expression of cyclooxygenase-2 mRNA via NFkappaB activation in human gingival fibroblasts. Arch Oral Biol 54: 251–7.
  39. 39. Wu HJ, Chi CW, Liu TY (2005) Effects of pH on nicotine-induced DNA damage and oxidative stress. J Toxicol Environ Health A 68: 1511–23.
  40. 40. Dong QG, Sclabas GM, Fujioka S, Schmidt C, Peng B, et al. (2002) The function of multiple IkappaB: NF-kappaB complexes in the resistance of cancer cells to Taxol-induced apoptosis. Oncogene 21: 6510–9.
  41. 41. Jetten AM (2009) Retinoid-related orphan receptors (RORs): critical roles in development, immunity, circadian rhythm, and cellular metabolism. Nucl Recept Signal 7: e003.
  42. 42. Abdallah A, Sato H, Grutters JC, Veeraraghavan S, Lympany PA, et al. (2003) Inhibitor kappa B-alpha (IkappaB-alpha) promoter polymorphisms in UK and Dutch sarcoidosis. Genes Immun 4: 450–4.