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Kim, Park, Kim, Park, Eun, Kwon, and Kim: Association of Toll-Like Receptor 2 Polymorphisms with Papillary Thyroid Cancer and Clinicopathologic Features in a Korean Population
Original Article
Oncology & Hematology
Journal of Korean Medical Science

Journal of Korean Medical Science 2012; 27(11): 1333-1338.

Published online: 30 October 2012

DOI: https://doi.org/10.3346/jkms.2012.27.11.1333

Association of Toll-Like Receptor 2 Polymorphisms with Papillary Thyroid Cancer and Clinicopathologic Features in a Korean Population

Mi Kyeong Kim1, Sung Wook Park1, Su Kang Kim2, Hae Jeong Park2, Young Gyu Eun3, Kee Hwan Kwon4, Jinju Kim2, 5

1Department of Anesthesiology and Pain Medicine, Kyung Hee University School of Medicine, Seoul, Korea.

2Kohwang Medical Research Institute, Kyung Hee University School of Medicine, Seoul, Korea.

3Department of Otolaryngology-Head and Neck Surgery, Kyung Hee University School of Medicine, Seoul, Korea.

4Department of Otorhinolaryngology-Head and Neck Surgery, Ilsong Memorial Institute of Head and Neck Cancer, Hallym University College of Medicine, Anyang, Korea.

5Department of Oriental Physiology, Kyung Hee University College of Pharmacy, Seoul, Korea.

Address for Correspondence: Jinju Kim, PhD. Department of Oriental Physiology, College of Pharmacy, School of Medicine and Kohwang Medical Research Institute, Kyung Hee University, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul 130-701, Korea. Tel: +82.2-961-9437, Fax: +82.2-968-0560, shdwer@khu.ac.kr

Received 4 January 2012       Accepted 27 August 2012

© 2012 The Korean Academy of Medical Sciences.

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Toll-like receptors (TLRs) single nucleotide polymorphisms (SNPs) were analyzed in patients with papillary thyroid cancer (PTC; n = 133) and their clinicopathologic features and age-matched controls (n = 321) using direct sequencing. PTC patients were divided into subgroups according to size, number, location, extrathyroidal invasion and lymph node metastasis. The two SNPs of TLR2 gene were not associated with the development of PTC. In clinical analysis, two SNPs were associated with location of cancer (rs3804099, P = 0.032, OR, 0.52; 95% CI, 0.28-0.96 in log-additive model; rs3804100, P = 0.039, OR, 0.46, 95% CI, 0.22-0.96 in codominant1 model; P = 0.018, OR, 0.42, 95% CI, 0.21-0.87 in dominant model; P = 0.011, OR, 0.46, 95% CI, 0.25-0.85 in log-additive model). The allele frequencies of two SNPs also showed significant associations with location of cancer (rs3804099, P = 0.046, OR, 0.57, 95% CI, 0.33-0.99 and rs3804100, P = 0.019, OR = 0.52, 95% CI = 0.30-0.90). However, two SNPs were not associated with the clinicopathologic features of PTC. It is suggested that TLR2 polymorphisms may contribute to the clinicopathologic features of PTC, especially the PTC in both lobes.

Keywords: Papillary Thyroid Cancer, Single Nucleotide Polymorphisms, Clinicopathologic Characteristics, Toll-Like Receptors

INTRODUCTION

Thyroid cancer is characterized by the most common endocrine malignant carcinoma and is one of the fastest growing cancer diagnoses worldwide. There are four major types of thyroid cancers that are clinically significant: papillary, follicular, anaplastic, and medullary thyroid cancers. Of these, papillary thyroid cancer (PTC) is the most common type, showed about 80% of all cases of thyroid cancer. It is well-known that ionizing radiation exposure is a main risk factor (1). However, the exact etiology of PTC has been still unknown.
The Toll-like receptors (TLRs) family of transmembrane receptors plays a fundamental role in pathogen recognition and activation of innate immunity. Ligation of TLRs results in substantial immune responses that may be directed against tumor-associated antigens (2). A latent role for radiation in signaling 'danger' and, perhaps, in the activation of antigen presenting cells on immune system has been suggested (3-6). Radiation may also activate effectors of innate immunity through TLR-dependent mechanisms, thereby up-regulate the adaptive immune response to cancer (2). The TLR2 gene is located in the chromosome 4p32 protein coding gene, and is expressed most abundantly in peripheral blood leukocytes, and mediates host response (http://www.ncbi.nlm.nih.gov/gene).
Hashimoto's thyroiditis is the most common gradual autoimmune-mediated thyroid failure and it is developed goiter at times. Some studies have found an association between Hashimoto's thyroiditis and PTC (7). Previous study was demonstrated that Hashimoto's thyroiditis was associated with an increased risk of developing PTC (7). Also, genetic factors seem to be involved as a risk factor for PTC (8-12). Indeed, several single nucleotide polymorphisms (SNPs) are thought to contribute to susceptibility to PTC (13-15).
In this study, we investigated whether synonymous SNPs in TLR2 contribute to the development of PTC. We also assessed the relationships between TLR2 SNPs and the clinicopathologic characteristics of PTC.

MATERIALS AND METHODS

Patients and controls

Study subjects consisted of PTC patients (n = 133, 48 males and 85 females) and controls (n = 321, 129 males and 192 females). The mean ages of the PTC and control groups were 54.7 ± 12.3 yr (mean ± SD) and 56.3 ± 11.9, respectively (Table 1). PTC patients were recruited among participants visiting Kyung Hee University Medical Center, Seoul, Republic of Korea. Control subjects were enrolled from healthy participants examined in a general health check-up program. Participants with cancers, thyroid diseases, or any other severe diseases were excluded. PTC diagnosis was confirmed by pathologic examination. Patients with anaplastic carcinoma, follicular carcinoma, double primary of PTC and follicular carcinoma, follicular variant of PTC, or nodular hyperplasia were excluded.

Patient subgroups

To assess the relationship between TLR2 SNPs and the clinical pathologic characteristics of PTC, patients were divided into subgroups according to the size (< 1 cm and ≥ 1 cm), number (unifocality and multifocality), location (one lobe and both lobes), extrathyroidal invasion (present and absent), and lymph node metastasis (present and absent). Demographic features of PTC patients are summarized in Table 1.

SNP selection and genotyping

For the selection among TLR2 SNPs, we searched the synonymous SNPs of the TLR2 gene in the SNP database of the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/SNP, BUILD132). Because 16 missense SNPs of the TLR2 gene had an unknown heterozygosity or minor allele frequency (MAF) below 0.05, all missense SNPs were excluded. Out of 13 synonymous SNPs of the TLR2 gene, there were 11 SNPs with MAF below 0.05. Finally, two SNPs (rs3804099, Asn199Asn; rs3804100, Ser132Ser) were selected. Blood samples for DNA extraction from all subjects were collected. Genomic DNA was extracted with 200 µL whole blood using DNA Isolation Kit for Cells and Tissues (Roche, Indianapolis, IN, USA) and stored at -20℃ before use. SNP genotyping was determined by direct sequencing. Polymerase chain reactions (PCRs) were performed using the primers for two synonymous SNPs (Table 2). PCR comprised 40 cycles at 94℃ for 30 sec, 58℃ for 30 sec, 72℃ for 30 sec, and 1 cycle at 72℃ for 5 min for the final reaction. The PCR products were sequenced by an ABI PRISM 3730XL analyzer (PE Applied Biosystems, Foster City, CA, USA). Sequencing data were analyzed using SeqManII software (DNASTAR, Madison, WI, USA).

Statistical analysis

Hardy-Weinberg equilibrium (HWE) was estimated using SNPStats (http://bioinfo.iconcologia.net/index.php?module=Snpstats) in both the patient and control groups. Multiple logistic regression models were applied to obtain odds ratios (ORs), 95% confidence intervals (CIs), and P values (codominant1, codominant2, dominant, recessive, and log-additive models). When the numbers of genotype and allele were less than 5, Fisher's exact test was performed. Data analysis was performed using SPSS 18.0 (SPSS, Chicago, IL, USA) and SNPstats (http://bioinfo.iconcologia.net/index.php?module=Snpstats). Linkage disequilibrium (LD) block and haplotypes were evaluated using Haploview version 4.2 (Daly Lab Inc., Cambridge, MA, USA). P < 0.05 was considered significant.

Ethics statement

This study was approved by the institutional review board of the Medical Research Institute, Kyung Hee University Medical Center, Seoul, Korea (20040915). Written informed consent was obtained from all subjects.

RESULTS

We genotyped two synonymous SNPs in the TLR2 gene. The genotype and allele frequencies of two synonymous SNPs are presented in Table 3. Multiple logistic regression analysis with adjustment for age and gender was performed: codominant1 (major allele homozygotes vs heterozygotes), codominant2 (major allele homozygotes vs minor allele homozygotes), dominant (major allele homozygotes vs heterozygotes + minor allele homozygotes), recessive (major allele homozygotes + heterozygotes vs minor allele homozygotes), and log-additive (major allele homozygotes vs heterozygotes vs minor allele homozygotes). The two SNPs were in Hardy-Weinberg equilibrium in the control group (rs3804099, P = 0.30; rs3804100, P = 0.11). Our two synonymous SNP in Table 3 (rs3804099, Asn199Asn; rs3804100, Ser132Ser) of TLR2 was not associated between control and PTC patients (rs3804099, P = 0.680 in allele [reference T vs C]; rs3804100, P = 0.850 in allele [reference T vs C]).
Next, we assessed the relationship between TLR2 SNPs and the clinical pathologic features of PTC. In the location of cancer (one lobe vs both lobes), the SNP (rs3804099) was related to location of PTC in genotype (rs3804099, P = 0.032, OR, 0.52; 95% CI, 0.28-0.96 in log-additive model [reference T/T vs T/C vs C/C]) and allele distributions (P = 0.046, OR, 0.57; 95% CI = 0.33-0.99, reference T vs C). Another SNP (rs3804100) was significantly associated with location of PTC in genotype (rs3804100, P = 0.039, OR, 0.46, 95% CI, 0.22-0.96 in codominant1 model [reference T/T vs T/C]; P = 0.018, OR, 0.42, 95% CI, 0.21-0.87 in dominant model [reference T/T vs T/C + C/C]; P = 0.011, OR, 0.46; 95% CI, 0.25-0.85 in log-additive model [reference T/T vs T/C vs C/C], respectively) and allele distributions (P = 0.019, OR, 0.52; 95% CI, 0.30-0.90, reference T vs C) (Table 4). However, no association was evident with clinical pathologic features of PTC (Tables 5, 6).
Linkage disequilibrium (LD) block between rs3804099 and rs3804100 was determined using Haploview version 4.2. Since the LD block was made (D' = 1.00 and r2 = 0.94, data not shown), the analysis of haplotypes was performed. The frequency of TT was 0.69, CC was 0.297 and CT was 0.013, however, the association was not observed (data not shown). We calculated sample power to verify our data (http://pngu.mgh.harvard.edu/~purcell/gpc/cc2.html). In this study, the sample power of each SNP was 0.745 (rs3804099, alpha level = 0.05, the number of cases for 70% power = 91) and 0.730 (rs3804100, alpha level = 0.05, the number of cases for 70% power = 95). These sample powers were sufficient to detect positive associations between SNPs and PTC.

DISCUSSION

The functions of TLRs have provided potential insight into the cancer development. TLR-dependent mechanisms contribute to activate effectors of innate, thereby augmenting the adaptive immune response to cancer (2, 16, 17).
Numerous studies have investigated TLR2 polymorphisms in different populations and different diseases with conflicting results. The two presently-studied TLR2 SNPs, rs3804099 and rs3804100, were reportedly associated with sarcoidosis with cutaneous manifestations in a Japanese population (18), and rs3804099 was suggested as a relevant risk estimate for the development of sepsis and multiple organ dysfunction in Chinese patients with major trauma (19). In addition, TLR2 -196 to -173 del, +597 T > C and +1350 T > C polymorphisms have been associated with asymptomatic bancroftian filariasis in Thailand (20). In a TLR2-related cancer study, SNPs of TLR2 were not associated with colorectal cancer in individuals of three races (20 Malays, 20 Chinese and 18 Indians) (21). On the contrary, the association with microsatellite GT polymorphisms of TLR2 gene and sporadic colorectal cancer among Croatians has been reported (22).
Here, we sought to determine the relationships between the TLR2 SNPs and PTC in a Korean population. We also assessed the relationships between TLR2 SNPs and the clinicopathologic characteristics of PTC. The findings of our study suggest that no significant differences exist in the frequency of TLR2 genotypes and alleles in the PTC cases comparison with the controls. However, TLR2 was associated with clinicopathologic features, especially in the locations of PTC. The T/T frequency of rs3804099 was different between the one lobe and both lobe groups (37.1% vs 54.0%, respectively). The T allele frequencies of rs3804099 in PTC patients with involvement of both lobes (75.4%) were higher than those in PTC patients with one lobe involvement (63.7%). The T allele frequencies of rs3804100 in PTC patients with involvement of both lobes (76.9%) were higher than those in PTC patients with involvement of one lobe (63.5%). Therefore, the T allele of rs3804099 and rs3804100 may be correlated with the location of PTC in the Korean population. Thyroid lobectomy alone may be sufficient treatment for small (<1 cm), low-risk, unifocal, intrathyroidal papillary carcinomas in the absence of prior head and neck irradiation or radiologically or clinically involved cervical nodal metastases. But patients who have bilateral PTC should undergo total thyroidectomy. Therefore, tumor bilaterality can be used to determine surgical extent (23). The relationship between TLR2 polymorphisms and cancer location is significant.
This study has some limitations. The sample size of patients is small and control subjects did not receive the thyroid ultra sonography. Considering that the incidence of thyroid cancer (0.5-10/100,000 persons) is relatively low, more studies with larger numbers of patients are needed to verify our results.
In conclusion, based on our case-control association study of SNPs in TLR2 genes in patients with PTC and control subjects, significant associations are reported between polymorphisms of the TLR2 gene and PTC in both lobes. The results suggest that the TLR2 polymorphisms may be associated with the clinicopathologic features of PTC in the Korean population, especially concerning the location of cancer.

Figures and Tables

Table 1
Clinical characteristics of the study population
jkms-27-1333-i001

PTC patients having inappropriate clinical data were excluded. Because of PTC patients having inappropriate clinical data, the total number of PTC phenotype are different. PTC, papillary thyroid cancer; No., number of subjects; SD, standard deviation.

Table 2
Primer sequences for each SNP
jkms-27-1333-i002

SNP, single nucleotide polymorphism; bp, base pair.

Table 3
Frequencies of genotype and allele of TLR2 in control and patients with papillary thyroid cancer (PTC)
jkms-27-1333-i003

The P values were calculated from logistic regression analyses adjusting sex and age (codominant1, A/A vs A/B; codominant2, A/A vs B/B; dominant A/A vs A/B+B/B; recessive, A/A+A/B vs B/B; log-additive, A/A vs A/B vs B/B). Missing data of genotype were excluded for exact analysis. PTC, papillary thyroid cancer; SNP, single nucleotide polymorphism; OR, odds ratio; CI, confidence interval.

Table 4
Genotype and allele frequencies of SNPs of TLR2 gene in PTC patients with one lobe and PTC patients with both lobes
jkms-27-1333-i004

The P values were calculated from logistic regression analyses adjusting sex and age (codominant1, A/A vs A/B; codominant2, A/A vs B/B; dominant A/A vs A/B+B/B; recessive, A/A+A/B vs B/B; log-additive, A/A vs A/B vs B/B). Bold numbers mean significance association. Missing data of genotype were excluded for exact analysis. PTC, papillary thyroid cancer; SNP, single nucleotide polymorphism; OR, odds ratio; CI, confidence interval.

Table 5
Genotype and allele frequencies of SNPs of TLR2 gene in PTC patients with tumor size < 1 cm and PTC patients with tumor size ≥ 1 cm
jkms-27-1333-i005

The P values were calculated from logistic regression analyses adjusting sex and age (codominant1, A/A vs A/B; codominant2, A/A vs B/B; dominant A/A vs A/B+B/B; recessive, A/A+A/B vs B/B; log-additive, A/A vs A/B vs B/B). Missing data of genotype were excluded for exact analysis. PTC, papillary thyroid cancer; SNP, single nucleotide polymorphism; OR, odds ratio; CI, confidence interval.

Table 6
Genotype and allele frequencies of SNPs of TLR2 gene in PTC patients with unifocality and PTC patients with multifocality
jkms-27-1333-i006

The P values were calculated from logistic regression analyses adjusting sex and age (codominant1, A/A vs A/B; codominant2, A/A vs B/B; dominant A/A vs A/B+B/B; recessive, A/A+A/B vs B/B; log-additive, A/A vs A/B vs B/B). Missing data of genotype were excluded for exact analysis. PTC, papillary thyroid cancer; SNP, single nucleotide polymorphism; OR, odds ratio; CI, confidence interval.

Notes

This research was supported by the Kyung Hee University Research Fund in 2010 (KHU-20101889).

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