Evidence map›Paper›PMID 26447841›Full record

ArticlePloS one2015

Circulating microRNA-200 Family as Diagnostic Marker in Hepatocellular Carcinoma.

Sameer A Dhayat, Anna Hüsing, Norbert Senninger, Hartmut H Schmidt, Jörg Haier, Heiner Wolters, Iyad Kabar

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Combinatorial Gene Expression Profiling of SerumInternational journal of molecular sciences · 2024
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  14. Up-regulation ofOncotarget · 2017
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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

7 authors at 1 institution in 1 country.

Sameer A DhayatDepartment of General and Visceral Surgery, University Hospital Muenster, Muenster, Germany.
Anna HüsingDepartment of Transplant Medicine, University Hospital Muenster, Muenster, Germany.
Norbert SenningerDepartment of General and Visceral Surgery, University Hospital Muenster, Muenster, Germany.
Hartmut H SchmidtDepartment of Transplant Medicine, University Hospital Muenster, Muenster, Germany.
Jörg HaierComprehensive Cancer Center Muenster, University Hospital Muenster, Muenster, Germany.
Heiner WoltersDepartment of General and Visceral Surgery, University Hospital Muenster, Muenster, Germany.
Iyad KabarDepartment of Transplant Medicine, University Hospital Muenster, Muenster, Germany.
University Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

goalsIn this clinical study, we aimed to evaluate the role of circulating microRNA-200 family as a non-invasive tool to identify patients with cirrhosis-associated hepatocellular carcinoma (HCC).

backgroundPrognosis of HCC remains poor with increasing incidence worldwide, mainly related to liver cirrhosis. So far, no reliable molecular targets exist for early detection of HCC at surgically manageable stages. Recently, we identified members of the microRNA-200 family as potential diagnostic markers of cirrhosis-associated HCC in patient tissue samples. Their value as circulating biomarkers for HCC remained undefined.

methodsBlood samples and clinicopathological data of consecutive patients with liver diseases were collected prospectively. Expression of the microRNA-200 family was investigated by qRT-PCR in blood serum samples of 22 HCC patients with and without cirrhosis. Serum samples of patients with non-cancerous chronic liver cirrhosis (n = 22) and of healthy volunteers (n = 15) served as controls.

resultsMicroRNA-141 and microRNA-200a were significantly downregulated in blood serum of patients with HCC compared to liver cirrhosis (p<0.007) and healthy controls (p<0.002). MicroRNA-141 and microRNA-200a could well discriminate patients with cirrhosis-associated HCC from healthy volunteers with area under the receiver-operating characteristic curve (AUC) values of 0.85 and 0.82, respectively. Additionally, both microRNAs could differentiate between HCC and non-cancerous liver cirrhosis with a fair accuracy.

conclusionsCirculating microRNA-200 family members are significantly deregulated in patients with HCC and liver cirrhosis. Further studies are necessary to confirm the diagnostic value of the microRNA-200 family as accurate serum marker for cirrhosis-associated HCC.

Indexed as

AdultAgedBiomarkers, TumorCarcinoma, HepatocellularCase-Control StudiesDiagnosis, DifferentialFemaleHumansLiver CirrhosisLiver NeoplasmsMaleMicroRNAsMiddle AgedROC CurveYoung AdultBiomarkers, TumorMicroRNAsMIRN141 microRNA, humanMIRN200 microRNA, human

Identifiers

PMID26447841
PMCPMC4598187
OpenAlexW2196829420

What OpenQuestion holds

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LicenceCC BY
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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.