Evidence map›Paper›PMID 25466449›Full record

ArticleDiagnostic pathology2014

Upregulation of microRNA-106b is associated with poor prognosis in hepatocellular carcinoma.

Bin-Kui Li, Pin-Zhu Huang, Ji-Liang Qiu, Ya-Di Liao, Jian Hong, Yun-Fei Yuan

Open access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  10. Serum miR-106b upregulation predicts poor prognosis in patients with colorectal cancer.International journal of clinical and experimental pathology · 2018
    Article
  11. Article
  12. Article
  13. Review
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  15. MicroRNA-155-3p promotes hepatocellular carcinoma formation by suppressing FBXW7 expression.Journal of experimental & clinical cancer research : CR · 2016
    Article
  16. Article
  17. Review
  18. 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

6 authors at 3 institutions in 1 country.

Bin-Kui LiState Key Laboratory of Oncology in South China, Guangzhou, China. libinkui@mail.sysu.edu.cn.
Pin-Zhu HuangState Key Laboratory of Oncology in South China, Guangzhou, China. pinzhuhuang@163.com.
Ji-Liang QiuState Key Laboratory of Oncology in South China, Guangzhou, China. jiliangqiu@163.com.
Ya-Di LiaoState Key Laboratory of Oncology in South China, Guangzhou, China. liaoyd@sysucc.org.cn.
Jian HongState Key Laboratory of Oncology in South China, Guangzhou, China. 05213625hj@sina.com.
Yun-Fei YuanState Key Laboratory of Oncology in South China, Guangzhou, China. yuanyf@mail.sysu.edu.cn.
Sun Yat-sen University · CNState Key Laboratory of Oncology in South ChinaSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNA-106b (miR-106b) is a member of the miR-106b ~ 25 cluster. It has been reported that miR-106b acts as an oncogene and is upregulated in many human cancers. However, the prognostic value of miR-106b in hepatocellular carcinoma (HCC) remains unclear. The aim of this study was to investigate the clinical significance of miR-106b expression in HCC.

methodsWe determined the expression level of miR-106b in 104 cases of paired HCC and adjacent non-tumor tissues by quantitative real-time PCR (qRT-PCR). The correlation between miR-106b expression and prognosis of HCC was studied by univariate and multivariate analysis. Multivariate analysis of the prognostic factors was performed with Cox proportional hazards model.

resultsMiR-106b expression was significantly upregulated in as high as 76.0% of HCC tissues, compared with their non-tumor counterparts (P < 0.001). High miR-106b expression was significantly associated with large tumor size (P = 0.019) and vascular invasion (P = 0.016). Kaplan-Meier analysis showed that patients with high miR-106b expression had a worse overall survival than patients with low miR-106b expression (log-rank P = 0.004). The multivariate Cox regression analysis indicated that miR-106b expression was an independent prognostic factor for overall survival (HR, 2.002; 95% CI, 1.130-6.977; P = 0.027).

conclusionOur data indicated that miR-106b expression was significantly upregulated in HCC and could serve as a potential unfavorable prognostic biomarker. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_226.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularChi-Square DistributionFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLiver NeoplasmsMaleMicroRNAsMiddle AgedMultivariate AnalysisNeoplasm InvasivenessPredictive Value of TestsPrognosisProportional Hazards ModelsBiomarkers, TumorMicroRNAsMIRN106 microRNA, human

Identifiers

PMID25466449
PMCPMC4261545
OpenAlexW2120193238

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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.