TY - JOUR
T1 - The genetic polymorphisms in the MIR17HG gene are associated with the risk of head and neck squamous cell carcinoma in the Chinese Han population
AU - Xu, Chongwen
AU - Han, Peng
AU - Ren, Wanli
AU - Dai, Hao
AU - Bai, Yanxia
AU - Shen, Zhen
AU - Li, Baiya
AU - Shao, Yuan
N1 - Publisher Copyright:
Copyright © 2020 Chongwen Xu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2020
Y1 - 2020
N2 - Purpose. Head and neck squamous cell carcinoma (HNSCC) is the most common malignant tumors in the world. Genetic variants have an important role in HNSCC progression. Our study is aimed at exploring the relationship between MIR17HG polymorphisms and HNSCC risk in the Chinese Han population. Methods. We recruited 537 HNSCC cases and 533 healthy subjects to detect the correlation of six polymorphisms in MIR17HG with HNSCC susceptibility. The associations were evaluated by computing odds ratios (ORs) and 95% confidence intervals (CIs) using logistic regression analysis. Results. Our study revealed that rs7336610 (OR 1.77, 95%CI = 1:09‐2:86, and p = 0:021) and rs1428 (OR 1.73, 95%CI = 1:07‐2:81, and p = 0:025) are strongly associated with increased susceptibility to HNSCC in men. Besides, rs17735387 played a crucial protective role in stage III/IV HNSCC patients (OR 0.34, 95%CI = 0:12‐0:95, and p = 0:040) compared with stage I/II. Conclusion. Our study firstly indicated that MIR17HG polymorphisms are significantly associated with HNSCC susceptibility, which suggests that MIR17HG has a potential role in the occurrence of HNSCC.
AB - Purpose. Head and neck squamous cell carcinoma (HNSCC) is the most common malignant tumors in the world. Genetic variants have an important role in HNSCC progression. Our study is aimed at exploring the relationship between MIR17HG polymorphisms and HNSCC risk in the Chinese Han population. Methods. We recruited 537 HNSCC cases and 533 healthy subjects to detect the correlation of six polymorphisms in MIR17HG with HNSCC susceptibility. The associations were evaluated by computing odds ratios (ORs) and 95% confidence intervals (CIs) using logistic regression analysis. Results. Our study revealed that rs7336610 (OR 1.77, 95%CI = 1:09‐2:86, and p = 0:021) and rs1428 (OR 1.73, 95%CI = 1:07‐2:81, and p = 0:025) are strongly associated with increased susceptibility to HNSCC in men. Besides, rs17735387 played a crucial protective role in stage III/IV HNSCC patients (OR 0.34, 95%CI = 0:12‐0:95, and p = 0:040) compared with stage I/II. Conclusion. Our study firstly indicated that MIR17HG polymorphisms are significantly associated with HNSCC susceptibility, which suggests that MIR17HG has a potential role in the occurrence of HNSCC.
UR - https://www.scopus.com/pages/publications/85097557334
U2 - 10.1155/2020/2329196
DO - 10.1155/2020/2329196
M3 - 文章
C2 - 33299861
AN - SCOPUS:85097557334
SN - 2314-6133
VL - 2020
JO - BioMed Research International
JF - BioMed Research International
M1 - 2329196
ER -