Pri-miR-124 rs531564 and pri-miR-34b/c rs4938723 polymorphisms are associated with decreased risk of esophageal squamous cell carcinoma in Chinese populations.
| dc.contributor.author | Zhang, Junjie | |
| dc.contributor.author | Huang, Xuewen | |
| dc.contributor.author | Xiao, Juanjuan | |
| dc.contributor.author | Yang, Yajun | |
| dc.contributor.author | Zhou, Yinghui | |
| dc.contributor.author | Wang, Xiaofeng | |
| dc.contributor.author | Liu, Qingmei | |
| dc.contributor.author | Yang, Jingmin | |
| dc.contributor.author | Wang, Mengyun | |
| dc.contributor.author | Qiu, Lixin | |
| dc.contributor.author | Zheng, Yabiao | |
| dc.contributor.author | Zhang, Ping | |
| dc.contributor.author | Li, Jin | |
| dc.contributor.author | Wang, Ya'nong | |
| dc.contributor.author | Wei, Qingyi | |
| dc.contributor.author | Jin, Li | |
| dc.contributor.author | Wang, Jiucun | |
| dc.contributor.author | Wang, Minghua | |
| dc.date.accessioned | 2019-02-01T15:17:02Z | |
| dc.date.available | 2019-02-01T15:17:02Z | |
| dc.date.issued | 2014-01 | |
| dc.date.updated | 2019-02-01T15:17:01Z | |
| dc.description.abstract | MicroRNAs are a new class of small non-protein-coding RNAs that sometimes function as tumor suppressors or oncogenes. Aberrant expression and structural alteration of microRNAs have been reported to be involved in tumorigenesis and cancer development. Recently, rs531564/pri-miR-124-1, rs4938723/pri-miR-34b/c, rs7372209/pri-miR-26a-1, rs895819/pre-miR-27a, and rs11134527/pri-miR-218 were reported to be associated with risks of various cancers. In order to evaluate the relationship of these SNPs and esophageal squamous cell carcinoma (ESCC) risk, we conducted a case-control study with 1109 ESCC patients and 1275 control subjects to examine the potential association of these pri/pre-miRNA polymorphisms with ESCC susceptibility. As a result, two SNPs were associated with a significant risk of ESCC. We found that the GG genotype of pri-miR-124-1 rs531564 was associated to a significantly decreased risk of ESCC comparing with the CC/CG genotypes (p = 0.005; OR = 0.61, 95% CI = 0.43-0.86). In addition, the CC genotype of pri-miR-34b/c rs4938723 was associated with a significant decreased risk of ESCC (CC VS.p = 0.007, OR = 0.82, 95% CI = 0.71-0.95) in Chinese population. The present study provides the first evidence that pri-miR-124-1 rs531564 and pri-miR-34 rs4938723 were associated with the risk of ESCC in Chinese population. | |
| dc.identifier | PONE-D-13-49490 | |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.issn | 1932-6203 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Public Library of Science (PLoS) | |
| dc.relation.ispartof | PloS one | |
| dc.relation.isversionof | 10.1371/journal.pone.0100055 | |
| dc.subject | Humans | |
| dc.subject | Carcinoma, Squamous Cell | |
| dc.subject | Esophageal Neoplasms | |
| dc.subject | Genetic Predisposition to Disease | |
| dc.subject | MicroRNAs | |
| dc.subject | Risk Factors | |
| dc.subject | Case-Control Studies | |
| dc.subject | Alcohol Drinking | |
| dc.subject | Smoking | |
| dc.subject | Polymorphism, Single Nucleotide | |
| dc.subject | Adult | |
| dc.subject | Aged | |
| dc.subject | Aged, 80 and over | |
| dc.subject | Middle Aged | |
| dc.subject | Asian Continental Ancestry Group | |
| dc.subject | China | |
| dc.subject | Female | |
| dc.subject | Male | |
| dc.subject | Genetic Association Studies | |
| dc.subject | Multifactor Dimensionality Reduction | |
| dc.title | Pri-miR-124 rs531564 and pri-miR-34b/c rs4938723 polymorphisms are associated with decreased risk of esophageal squamous cell carcinoma in Chinese populations. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Wei, Qingyi|0000-0002-3845-9445|0000-0003-4115-4439 | |
| pubs.begin-page | e100055 | |
| pubs.issue | 6 | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Population Health Sciences | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Medicine, Medical Oncology | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.publication-status | Published | |
| pubs.volume | 9 |
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