Evidence map›Paper›PMID 26457018›Full record

ReviewWorld journal of gastroenterology2015

Genetic and epigenetic aspects of initiation and progression of hepatocellular carcinoma.

Mitsuro Kanda, Hiroyuki Sugimoto, Yasuhiro Kodera

Open access · bronzeAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. miRNAs in HCC, pathogenesis, and targets.Hepatology (Baltimore, Md.) · 2024
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  11. Review
  12. RANBP2 ActivatesCancers · 2021
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  14. Journal of Cancer · 2021
    Article
  15. Article
  16. Article
  17. Expression and Prognostic Significance of m6A-Related Genes in Lung Adenocarcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  18. Article
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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

3 authors at 1 institution in 1 country.

Mitsuro KandaMitsuro Kanda, Hiroyuki Sugimoto, Yasuhiro Kodera, Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Hiroyuki SugimotoMitsuro Kanda, Hiroyuki Sugimoto, Yasuhiro Kodera, Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Yasuhiro KoderaMitsuro Kanda, Hiroyuki Sugimoto, Yasuhiro Kodera, Department of Gastroenterological Surgery (Surgery II), Nagoya University Graduate School of Medicine, Nagoya 466-8550, Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a primary cancer of the liver that is predominant in developing countries and is responsible for nearly 600000 deaths each year worldwide. Similar to many other tumors, the development of HCC must be understood as a multistep process involving the accumulation of genetic and epigenetic alterations in regulatory genes, leading to the activation of oncogenes and the inactivation or loss of tumor suppressor genes. Extensive research over the past decade has identified a number of molecular biomarkers, including aberrant expression of HCC-related genes and microRNAs. The challenge facing HCC research and clinical care at this time is to address the heterogeneity and complexity of these genetic and epigenetic alterations and to use this information to direct rational diagnosis and treatment strategies. The multikinase inhibitor sorafenib was the first molecularly targeted drug for HCC to show some extent of survival benefits in patients with advanced tumors. Although the results obtained using sorafenib support the importance of molecular therapies in the treatment of HCC, there is still room for improvement. In addition, no molecular markers for drug sensitivity, recurrence and prognosis are currently clinically available. In this review, we provide an overview of recently published articles addressing HCC-related genes and microRNAs to update what is currently known regarding genetic and epigenetic aspects of the pathogenesis of HCC and propose novel promising candidates for use as diagnostic and therapeutic targets in HCC.

Indexed as

Epigenesis, GeneticGene Expression Regulation, NeoplasticAnimalsCarcinoma, HepatocellularCell Cycle ProteinsDisease ProgressionDNA MethylationGenes, Tumor SuppressorHumansInterleukin-6Liver NeoplasmsMembrane GlycoproteinsMicrotubule-Associated ProteinsNeoplasm Recurrence, LocalNiacinamideNuclear ProteinsCell Cycle ProteinsInterleukin-6MACC1 protein, humanMembrane GlycoproteinsMicrotubule-Associated ProteinsNiacinamideNuclear ProteinsPhenylurea CompoundsReceptors, ImmunologicSirtuin 1SorafenibTPX2 protein, humanTrans-ActivatorsTranscription FactorsTREM1 protein, humanTriggering Receptor Expressed on Myeloid Cells-1DNA methylationHepatocellular carcinomaMicroRNAOncogeneTumor suppressor gene

Identifiers

PMID26457018
PMCPMC4588080
OpenAlexW2414125851

What OpenQuestion holds

Textmetadata
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.