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Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma
Background: As the sixth most common cancer of worldwide, head and neck cancers (HNC) are springing from oral cavity, pharynx and larynx and there is no strong biomarker for prognosis. Rates of 5 years survival with HNC remain relatively low in decades with improvement of treatments. Evidence that s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099049/ https://www.ncbi.nlm.nih.gov/pubmed/32266149 http://dx.doi.org/10.3389/fonc.2020.00372 |
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author | He, Yingzheng Ji, Pei Li, Yuancheng Wang, Ruixia Ma, Hongxia Yuan, Hua |
author_facet | He, Yingzheng Ji, Pei Li, Yuancheng Wang, Ruixia Ma, Hongxia Yuan, Hua |
author_sort | He, Yingzheng |
collection | PubMed |
description | Background: As the sixth most common cancer of worldwide, head and neck cancers (HNC) are springing from oral cavity, pharynx and larynx and there is no strong biomarker for prognosis. Rates of 5 years survival with HNC remain relatively low in decades with improvement of treatments. Evidence that single nucleotide polymorphisms (SNPs) play a part in cancer prognosis is growing. Methods: We conducted an exome-wide association study among 261 patients with head and neck squamous cell carcinoma (HNSCC) and then validated in The Cancer Genome Atlas (TCGA) database for survival by using the Cox proportional hazards regression models and Kaplan–Meier analyses. Results: After combining the result of the two stages, 4 SNPs were significantly associated with HNSCC survival (rs16879870 at 6q14.3: adjusted HR = 2.02, 95%CI = 1.50–2.73, P = 3.88 × 10(−6); rs2641256 at 17p13.2: adjusted HR = 0.67, 95%CI = 0.56–0.80, P = 7.51 × 10(−6); rs2761591 at 11p13: adjusted HR = 2.07, 95%CI = 1.50–2.87, P = 1.16 × 10(−5); and rs854936 at 22q11.21: adjusted HR = 1.92, 95%CI = 1.43–2.57, P = 1.27 × 10(−5)). Besides, we constructed a receiver operating characteristic (ROC) model to estimate predictive effect of the novel SNPs combined with clinical stage in HNSCC prognosis (AUC = 0.715). We also found the genotype of rs16879870 and rs854936 was significantly associated with the expression of gene GJB7 (P = 0.013) and RTN4R (P = 0.047) in cancer tissues of TCGA, respectively. Conclusion: Our findings suggested that the SNPs (rs16879870, rs2641256, rs2761591, rs854936) might play a crucial role in prognosis of HNSCC. |
format | Online Article Text |
id | pubmed-7099049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70990492020-04-07 Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma He, Yingzheng Ji, Pei Li, Yuancheng Wang, Ruixia Ma, Hongxia Yuan, Hua Front Oncol Oncology Background: As the sixth most common cancer of worldwide, head and neck cancers (HNC) are springing from oral cavity, pharynx and larynx and there is no strong biomarker for prognosis. Rates of 5 years survival with HNC remain relatively low in decades with improvement of treatments. Evidence that single nucleotide polymorphisms (SNPs) play a part in cancer prognosis is growing. Methods: We conducted an exome-wide association study among 261 patients with head and neck squamous cell carcinoma (HNSCC) and then validated in The Cancer Genome Atlas (TCGA) database for survival by using the Cox proportional hazards regression models and Kaplan–Meier analyses. Results: After combining the result of the two stages, 4 SNPs were significantly associated with HNSCC survival (rs16879870 at 6q14.3: adjusted HR = 2.02, 95%CI = 1.50–2.73, P = 3.88 × 10(−6); rs2641256 at 17p13.2: adjusted HR = 0.67, 95%CI = 0.56–0.80, P = 7.51 × 10(−6); rs2761591 at 11p13: adjusted HR = 2.07, 95%CI = 1.50–2.87, P = 1.16 × 10(−5); and rs854936 at 22q11.21: adjusted HR = 1.92, 95%CI = 1.43–2.57, P = 1.27 × 10(−5)). Besides, we constructed a receiver operating characteristic (ROC) model to estimate predictive effect of the novel SNPs combined with clinical stage in HNSCC prognosis (AUC = 0.715). We also found the genotype of rs16879870 and rs854936 was significantly associated with the expression of gene GJB7 (P = 0.013) and RTN4R (P = 0.047) in cancer tissues of TCGA, respectively. Conclusion: Our findings suggested that the SNPs (rs16879870, rs2641256, rs2761591, rs854936) might play a crucial role in prognosis of HNSCC. Frontiers Media S.A. 2020-03-20 /pmc/articles/PMC7099049/ /pubmed/32266149 http://dx.doi.org/10.3389/fonc.2020.00372 Text en Copyright © 2020 He, Ji, Li, Wang, Ma and Yuan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology He, Yingzheng Ji, Pei Li, Yuancheng Wang, Ruixia Ma, Hongxia Yuan, Hua Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title | Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title_full | Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title_fullStr | Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title_full_unstemmed | Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title_short | Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma |
title_sort | genetic variants were associated with the prognosis of head and neck squamous carcinoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099049/ https://www.ncbi.nlm.nih.gov/pubmed/32266149 http://dx.doi.org/10.3389/fonc.2020.00372 |
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