Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variants in miR-196a2 and miR-499 are associated with susceptibility to esophageal squamous cell carcinoma in Chinese Han population.

Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine - 1 Apr 2016

Shen Fangyuan, Chen Jiejun, Guo Shicheng, Zhou Yinghui, Zheng Yabiao, Yang Yajun, Zhang Junjie, Wang Xiaofeng, Wang Chenji, Zhao Dunmei, Wang Mengyun, Zhu Meiling, Fan Lixia, Xiang Jiaqing, Xia Yong, Wei Qingyi, Jin Li, Wang Jiucun, Wang Minghua

Abstract excerpt

Esophageal squamous cell carcinoma (ESCC) is the dominant type of esophageal cancer in the East Asian population. MicroRNAs (miRNAs) have been studied to play important roles in tumorigenesis. Single nucleotide polymorphisms (SNPs) in miRNA lead to the aberrant expression and structural alteration of miRNA and are hypothesized to be involved in tumorigenesis and cancer development. We conducted a population-based...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to Carcinoma, Squamous Cell

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Esophageal Neoplasms

Share to Genetic Association Studies

Share to MicroRNAs

Share to Models, Genetic

Share to ROC Curve

Source

Identifiers

PMID: 26518769
DOI: 10.1007/s13277-015-4268-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variants in miR-196a2 and miR-499 are associated with susceptibility to esophageal squamous cell carcinoma in Chinese Han population.PMID 26518769Read ↗

MiR-196a2 rs11614913 T > C polymorphism and risk of esophageal cancer in a Chinese population.Semantic proximity Read ↗

Association between miR-146a rs2910164, miR-196a2 rs11614913, and miR-499 rs3746444 polymorphisms and the risk of esophageal carcinoma: A case-control study.Semantic proximity Read ↗

A functional variation in pre-microRNA-196a is associated with susceptibility of esophageal squamous cell carcinoma risk in Chinese Han.Semantic proximity Read ↗

Hsa-miR-196a2 functional SNP is associated with the risk of ESCC in individuals under 60 years old.Semantic proximity Read ↗

MicroRNAs related polymorphisms and genetic susceptibility to esophageal squamous cell carcinoma.Semantic proximity Read ↗

miR-449b rs10061133 and miR-4293 rs12220909 polymorphisms are associated with decreased esophageal squamous cell carcinoma in a Chinese population.Semantic proximity Read ↗

A genetic variant in microRNA-196a2 is associated with increased cancer risk: a meta-analysis.Semantic proximity Read ↗

Contributions of polymorphisms in miR146a, miR196a, and miR499 to the development of hepatocellular carcinoma.Semantic proximity Read ↗

Comprehensive review of genetic association studies and meta-analyses on miRNA polymorphisms and cancer risk.Semantic proximity Read ↗

A genetic variant in miR-196a2 increased digestive system cancer risks: a meta-analysis of 15 case-control studies.Semantic proximity Read ↗

Quantitative assessment of the association between miR-196a2 rs11614913 polymorphism and cancer risk: evidence based on 45,816 subjects.Semantic proximity Read ↗

Association of microRNA polymorphisms with the risk of head and neck squamous cell carcinoma in a Chinese population: a case-control study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.