Evidence map›Paper›PMID 32483162›Full record

ArticleScientific reports2020

A computational drug repositioning method applied to rare diseases: Adrenocortical carcinoma.

Maryam Lotfi Shahreza, Nasser Ghadiri, James R Green

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 21 citations in OpenAlex.

  1. AΙ-Driven Drug Repurposing: Applications and Challenges.Medicines (Basel, Switzerland) · 2025
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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 2 institutions in 2 countries.

Maryam Lotfi ShahrezaDepartment of Electrical and Computer Engineering, Isfahan University of Technology, Isfahan, 84156-83111, Iran.
Nasser GhadiriDepartment of Electrical and Computer Engineering, Isfahan University of Technology, Isfahan, 84156-83111, Iran. nghadiri@iut.ac.ir.ORCID http://orcid.org/0000-0002-6519-6548
James R GreenDepartment of Systems and Computer Engineering, Carleton University, Ottawa, K1S 5B6, Canada.ORCID http://orcid.org/0000-0002-6039-2355
Isfahan University of Technology · IRCarleton University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rare or orphan diseases affect only small populations, thereby limiting the economic incentive for the drug development process, often resulting in a lack of progress towards treatment. Drug repositioning is a promising approach in these cases, due to its low cost. In this approach, one attempts to identify new purposes for existing drugs that have already been developed and approved for use. By applying the process of drug repositioning to identify novel treatments for rare diseases, we can overcome the lack of economic incentives and make concrete progress towards new therapies. Adrenocortical Carcinoma (ACC) is a rare disease with no practical and definitive therapeutic approach. We apply Heter-LP, a new method of drug repositioning, to suggest novel therapeutic avenues for ACC. Our analysis identifies innovative putative drug-disease, drug-target, and disease-target relationships for ACC, which include Cosyntropin (drug) and DHCR7, IGF1R, MC1R, MAP3K3, TOP2A (protein targets). When results are analyzed using all available information, a number of novel predicted associations related to ACC appear to be valid according to current knowledge. We expect the predicted relations will be useful for drug repositioning in ACC since the resulting ranked lists of drugs and protein targets can be used to expedite the necessary clinical processes.

Indexed as

Adrenal Cortex NeoplasmsAdrenocortical CarcinomaComputational BiologyCosyntropinDNA Topoisomerases, Type IIDrug RepositioningHumansOxidoreductases Acting on CH-CH Group DonorsPoly-ADP-Ribose Binding ProteinsReceptor, IGF Type 17-dehydrocholesterol reductaseCosyntropinDNA Topoisomerases, Type IIIGF1R protein, humanOxidoreductases Acting on CH-CH Group DonorsPoly-ADP-Ribose Binding ProteinsReceptor, IGF Type 1TOP2A protein, human

Identifiers

PMID32483162
PMCPMC7264316
OpenAlexW3029577894

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.