Evidence map›Paper›PMID 35326724›Full record

ArticleCancers2022

A Gene Co-Expression Network-Based Drug Repositioning Approach Identifies Candidates for Treatment of Hepatocellular Carcinoma.

Meng Yuan, Koeun Shong, Xiangyu Li, Sajda Ashraf, Mengnan Shi, Woonghee Kim, Jens Nielsen, Hasan Turkez, Saeed Shoaie, Mathias Uhlen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Identification ofFrontiers in immunology · 2024
    Article
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  9. Non-canonical NLRC4 inflammasomes in astrocytes contribute to glioma malignancy.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  10. Review
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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

12 authors at 4 institutions in 5 countries.

Meng YuanScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.ORCID 0000-0002-9248-3294
Koeun ShongScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.
Xiangyu LiScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.ORCID 0000-0002-8301-9959
Sajda AshrafHeka Lab, Camlik Mah. Hearty, Sk. No:4 Heka Human Plaza Umraniye, Istanbul 34774, Turkey.ORCID 0000-0003-4378-2754
Mengnan ShiScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.ORCID 0000-0001-8643-5846
Woonghee KimScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.
Jens NielsenDepartment of Biology and Biological Engineering, Chalmers University of Technology, SE-41296 Gothenburg, Sweden.
Hasan TurkezDepartment of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum 25240, Turkey.
Saeed ShoaieScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.
Mathias UhlenScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.
Cheng ZhangScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.ORCID 0000-0002-3721-8586
Adil MardinogluScience for Life Laboratory, KTH-Royal Institute of Technology, SE-17165 Stockholm, Sweden.ORCID 0000-0002-4254-6090
Science for Life Laboratory · SEKing's College London · GBAtatürk University · TRBioInnovation Institute · DK

Funding

China Scholarship Council 202006940003Knut and Alice Wallenberg Foundation 72110
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a malignant liver cancer that continues to increase deaths worldwide owing to limited therapies and treatments. Computational drug repurposing is a promising strategy to discover potential indications of existing drugs. In this study, we present a systematic drug repositioning method based on comprehensive integration of molecular signatures in liver cancer tissue and cell lines. First, we identify robust prognostic genes and two gene co-expression modules enriched in unfavorable prognostic genes based on two independent HCC cohorts, which showed great consistency in functional and network topology. Then, we screen 10 genes as potential target genes for HCC on the bias of network topology analysis in these two modules. Further, we perform a drug repositioning method by integrating the shRNA and drug perturbation of liver cancer cell lines and identifying potential drugs for every target gene. Finally, we evaluate the effects of the candidate drugs through an in vitro model and observe that two identified drugs inhibited the protein levels of their corresponding target genes and cell migration, also showing great binding affinity in protein docking analysis. Our study demonstrates the usefulness and efficiency of network-based drug repositioning approach to discover potential drugs for cancer treatment and precision medicine approach.

Indexed as

co-expression networkdrug repositioninghepatocellular carcinoma (HCC)survival analysissystems biology

Identifiers

PMID35326724
PMCPMC8946504
OpenAlexW4221006405

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.