Evidence map›Paper›PMID 36768566›Full record

ArticleInternational journal of molecular sciences2023

Guiding Drug Repositioning for Cancers Based on Drug Similarity Networks.

Shimei Qin, Wan Li, Hongzheng Yu, Manyi Xu, Chao Li, Lei Fu, Shibin Sun, Yuehan He, Junjie Lv, Weiming He and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. International journal of molecular sciences · 2023
    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

11 authors.

Shimei QinCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Wan LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.ORCID 0000-0002-9797-0315
Hongzheng YuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Manyi XuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Chao LiCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Lei FuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Shibin SunCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Yuehan HeCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Junjie LvCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.
Weiming HeInstitute of Opto-Electronics, Harbin Institute of Technology, Harbin 150001, China.
Lina ChenCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China.

Funding

Heilongjiang Postdoctoral Funds for Scientific Research Initiation LBH-Q17132National Natural Science Foundation of China 61702141National Natural Science Foundation of China 81627901Natural Science Foundation of Heilongjiang Province LH2021F043
6 · The paper itself

Abstract

Drug repositioning aims to discover novel clinical benefits of existing drugs, is an effective way to develop drugs for complex diseases such as cancer and may facilitate the process of traditional drug development. Meanwhile, network-based computational biology approaches, which allow the integration of information from different aspects to understand the relationships between biomolecules, has been successfully applied to drug repurposing. In this work, we developed a new strategy for network-based drug repositioning against cancer. Combining the mechanism of action and clinical efficacy of the drugs, a cancer-related drug similarity network was constructed, and the correlation score of each drug with a specific cancer was quantified. The top 5% of scoring drugs were reviewed for stability and druggable potential to identify potential repositionable drugs. Of the 11 potentially repurposable drugs for non-small cell lung cancer (NSCLC), 10 were confirmed by clinical trial articles and databases. The targets of these drugs were significantly enriched in cancer-related pathways and significantly associated with the prognosis of NSCLC. In light of the successful application of our approach to colorectal cancer as well, it provides an effective clue and valuable perspective for drug repurposing in cancer.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsComputational BiologyDrug RepositioningHumansAntineoplastic Agentsdrug repositioningdrug similarity networkNSCLCRandom Walk with Restart

Identifiers

PMID36768566
PMCPMC9917231

What Socratic 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 Socratic graph.