Evidence map›Paper›PMID 26886638›Full record

Observational studyMedicine2016

The Associations of Single Nucleotide Polymorphisms in miR196a2, miR-499, and miR-608 With Breast Cancer Susceptibility: A STROBE-Compliant Observational Study.

Zhi-Ming Dai, Hua-Feng Kang, Wang-Gang Zhang, Hong-Bao Li, Shu-Qun Zhang, Xiao-Bin Ma, Shuai Lin, Meng Wang, Yan-Jing Feng, Kang Liu and 3 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 8 pooled it
3.3field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 8 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  8. Effect ofTechnology in cancer research & treatment
    Pooled it
  9. Genetic variations in tumor-suppressor miRNA-encoding genes and their target genes: focus on breast cancer development and possible therapeutic strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
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  19. A New Method for BiostatisticalJournal of healthcare engineering · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Zhi-Ming DaiFrom the Department of Anesthesiology, Department of Hematology (Z-MD), Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an; Department of Oncology (H-FK, S-QZ, X-BM, SL, MW, Y-JF, KL, X-HL, PX, Z-JD), Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an; Department of Hematology (W-GZ), Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an; Department of Physiology and Pathophysiology (H-BL), Xi'an Jiaotong University School of Basic Medical Sciences, Xi'an Jiaotong University Cardiovascular Research Center, Xi'an Jiaotong University Health Science Center, Xi'an, China.
Hua-Feng Kang
Wang-Gang Zhang
Hong-Bao Li
Shu-Qun Zhang
Xiao-Bin Ma
Shuai Lin
Meng Wang
Yan-Jing Feng
Kang Liu
Xing-Han Liu
Peng Xu
Zhi-Jun Dai
China XD Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) play an important role as regulators of tumor suppressors and oncogenes in cancer-related processes. Single nucleotide polymorphisms (SNPs) in miRNAs have been shown to be relevant to various different cancers, including breast cancer (BC). The aim of this study was to estimate the associations between miRNA-related gene polymorphisms (miR-196a2, miR-499, and miR-608) and the risk of BC in a Chinese population. Gene polymorphisms were analyzed in 1143 subjects (controls = 583; BC = 560). The 3 SNPs were genotyped using the Sequenom Mass-ARRAY platform. The associations between the SNP frequencies and BC were assessed by computing odds ratios (ORs) and 95% confidence intervals (95% CIs), as well as by applying Chi-square tests. The miR-196a2 (rs11614913) T allele was associated with a decreased risk of BC based on results from dominant (OR = 0.67, 95% CI = 0.52-0.86), recessive (OR = 0.65, 95% CI = 0.48-0.86), and allele models (OR = 0.73, 95% CI = 0.62-0.86). In contrast, the miR-499 (rs3746444) AG/GG genotypes were associated with an increased risk of BC (OR = 1.45, 95% CI = 1.10-1.91), and miR-608 (rs4919510) was not significantly associated with BC risk. Our study suggested that the polymorphisms of rs11614913 and rs3746444 may be associated with BC risk in Chinese individuals.

Indexed as

AdultAsian PeopleBreast NeoplasmsCase-Control StudiesChinaFemaleGenetic Predisposition to DiseaseHumansMicroRNAsMiddle AgedPolymorphism, Single NucleotideMicroRNAsMIRN196 microRNA, humanMIRN499 microRNA, humanMIRN608 microRNA, human

Identifiers

PMID26886638
PMCPMC4998638
OpenAlexW2313592455

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.