Evidence map›Paper›PMID 27825117›Full record

ArticleOncotarget2016

Genetic variants in microRNAs predict non-small cell lung cancer prognosis in Chinese female population in a prospective cohort study.

Xia Lingzi, Yin Zhihua, Li Xuelian, Ren Yangwu, Zhang Haibo, Zhao Yuxia, Zhou Baosen

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Knockdown of Long Non-Coding RNACancer management and research · 2020
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Repression of Toll-like receptor-4 by microRNA-149-3p is associated with smoking-related COPD.International journal of chronic obstructive pulmonary disease · 2017
    Article
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

7 authors.

Xia LingziDepartment of Epidemiology, China Medical University, Shenyang, Liaoning, 110122, Peoples R China.
Yin ZhihuaDepartment of Epidemiology, China Medical University, Shenyang, Liaoning, 110122, Peoples R China.
Li XuelianDepartment of Epidemiology, China Medical University, Shenyang, Liaoning, 110122, Peoples R China.
Ren YangwuDepartment of Epidemiology, China Medical University, Shenyang, Liaoning, 110122, Peoples R China.
Zhang HaiboDepartment of Radiotherapy, Shenyang North Hospital, Shenyang, Liaoning, 110001, Peoples R China.
Zhao YuxiaDepartment of Radiotherapy Oncology, The Fourth Affiliated Hospital of China Medical University, Shenyang, Liaoning, 110001, Peoples R China.
Zhou BaosenDepartment of Epidemiology, China Medical University, Shenyang, Liaoning, 110122, Peoples R China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the prognostic effect of microRNA single nucleotide polymorphisms (SNP) on non-small cell lung cancer (NSCLC) patients, 658 female participants from northeast China were enrolled in our prospective cohort study and followed up from 2010 to 2015. C-containing genotypes of miR-149 rs2292832 were associated with better overall survival (OS). The joint effect of miR-149 and miR-196a2 and the joint effect of miR-149 and miR-608 were also observed in our study. To verify the function of miR-149 rs2292832, A549 cell lines were stably transfected with lenti-virus containing miR-149-C vector, miR-149-T vector and empty vector. Cells containing C allele assumed a higher expression level of miR-149, a decrease in cell growth and the sensitivity to anticancer drug when compared with cells containing T allele. The role of miR-149 playing in cancer prognosis may function through DNA topoisomerases 1 (TOP1) pathway, according to the results from luciferase reporter assays. In conclusion, miR-149 C allele may be a prognostic biomarker for better NSCLC OS.

Indexed as

Polymorphism, Single NucleotideA549 CellsAntineoplastic AgentsAsian PeopleBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell ProliferationChinaCisplatinDNA Topoisomerases, Type IDose-Response Relationship, DrugFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansKaplan-Meier EstimateAntineoplastic AgentsBiomarkers, TumorCisplatinDNA Topoisomerases, Type IMicroRNAsMIRN149 microRNA, humanMIRN196 microRNA, humanMIRN608 microRNA, humanTOP1 protein, humanChineselung cancermiRNAprognosisSNP

Identifiers

PMID27825117
PMCPMC5347756

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Registered trials

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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.