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Article

Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations

  • Authors:
    • Yuli Christine Chang
    • Ya-Sian Chang
    • Chun-Chi Chang
    • Ta-Chih Liu
    • Ying-Chin Ko
    • Chien-Chin Lee
    • Shun-Jen Chang
    • Jan-Gowth Chang
  • View Affiliations / Copyright

    Affiliations: Graduate Institute of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan, R.O.C., Epigenome Research Center, China Medical University Hospital, Taichung, Taiwan, R.O.C., Division of Chest Medicine, Department of Internal Medicine, Changhua Christian Hospital, Changhua, Taiwan, R.O.C., Graduate Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan, R.O.C., Environment-Omics‑Disease Research Center, China Medical University Hospital, Taichung, Taiwan, R.O.C., Department of Kinesiology, Health and Leisure Studies, National University of Kaohsiung, Kaohsiung, Taiwan, R.O.C.
  • Pages: 2936-2942
    |
    Published online on: March 8, 2016
       https://doi.org/10.3892/or.2016.4662
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Abstract

Tumor necrosis factor, α-induced protein 3 (TNFAIP3) which encodes a ubiquitin-modifying enzyme (A20), acts as a negative regulator of the NF-κB pathway, and in lymphoma and autoimmune diseases it is frequently inactivated by mutations and/or deletions. We investigated the prevalence of the inactivation of TNFAIP3 in oral squamous cell carcinoma (OSCC). DNA was extracted from 81 cases of OSCC and 50 peripheral blood samples from normal controls. A high-resolution melting (HRM) analysis was used to characterize TNFAIP3 mutations, and the results were confirmed by direct DNA sequencing. Three mutations and three single-nucleotide polymorphisms (SNPs) were found to be associated with OSCC; the TNFAIP3 mutation occurred in 3.7% (3/81) of the OSCC cases examined. All mutations were in exon 7 [c.1081G>A (p.E361K), c.1398C>G (p.S466R) (rs200878487) and c.1760C>T (p.P587L) (rs150056192)], and p.E361K was identified as a novel mutation. We further used SIFT and PolyPhen-2 software to assess potentially functional mutations. Two SNPs, c.296‑20_296-18delCTC (rs71670547) and c.380T>G (p.F127C) (rs2230926), were located in exon 3, and c.2140C>T (p.P714S) was located in exon 9. A novel SNP, p.P714S differed from the one reported previously (p.P714A) (rs369155845) at that site. We also identified five SNPs in 50 normal Taiwanese individuals, and two of them [c.296‑15C>T (rs377482653) and c.305A>G (p.N102S) (rs146534657)] were not found in our OSCC tissue. HRM facilitated the screening of genetic changes. In addition, our results indicate that the prevalence of the TNFAIP3 mutation is low in OSCC.
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Copy and paste a formatted citation
Spandidos Publications style
Chang YC, Chang Y, Chang C, Liu T, Ko Y, Lee C, Chang S and Chang J: Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations. Oncol Rep 35: 2936-2942, 2016.
APA
Chang, Y.C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C. ... Chang, J. (2016). Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations. Oncology Reports, 35, 2936-2942. https://doi.org/10.3892/or.2016.4662
MLA
Chang, Y. C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C., Chang, S., Chang, J."Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations". Oncology Reports 35.5 (2016): 2936-2942.
Chicago
Chang, Y. C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C., Chang, S., Chang, J."Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations". Oncology Reports 35, no. 5 (2016): 2936-2942. https://doi.org/10.3892/or.2016.4662
Copy and paste a formatted citation
x
Spandidos Publications style
Chang YC, Chang Y, Chang C, Liu T, Ko Y, Lee C, Chang S and Chang J: Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations. Oncol Rep 35: 2936-2942, 2016.
APA
Chang, Y.C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C. ... Chang, J. (2016). Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations. Oncology Reports, 35, 2936-2942. https://doi.org/10.3892/or.2016.4662
MLA
Chang, Y. C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C., Chang, S., Chang, J."Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations". Oncology Reports 35.5 (2016): 2936-2942.
Chicago
Chang, Y. C., Chang, Y., Chang, C., Liu, T., Ko, Y., Lee, C., Chang, S., Chang, J."Development of a high-resolution melting method for the screening of TNFAIP3 gene mutations". Oncology Reports 35, no. 5 (2016): 2936-2942. https://doi.org/10.3892/or.2016.4662
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