Evidence map›Paper›PMID 35013135›Full record

ArticleCell death discovery2022

Transcription Factor Activation Profiles (TFAP) identify compounds promoting differentiation of Acute Myeloid Leukemia cell lines.

Federica Riccio, Elisa Micarelli, Riccardo Secci, Giulio Giuliani, Simone Vumbaca, Giorgia Massacci, Luisa Castagnoli, Claudia Fuoco, Gianni Cesareni

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2022. 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
0.4field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 1 institution in 1 country.

Federica Riccio *University of Rome "Tor Vergata", Department of Biology, Rome, Italy. federicariccio1989@libero.it.ORCID http://orcid.org/0000-0003-2939-3306
Elisa Micarelli *University of Rome "Tor Vergata", Department of Biology, Rome, Italy.
Riccardo SecciUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy.ORCID http://orcid.org/0000-0002-4562-703X
Giulio GiulianiUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy.ORCID http://orcid.org/0000-0002-4648-0076
Simone VumbacaUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy.ORCID http://orcid.org/0000-0003-1940-3355
Giorgia MassacciUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy.ORCID http://orcid.org/0000-0003-3223-6547
Luisa CastagnoliUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy.
Claudia FuocoUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy. claudia.fuoco@uniroma2.it.ORCID http://orcid.org/0000-0001-8372-305X
Gianni CesareniUniversity of Rome "Tor Vergata", Department of Biology, Rome, Italy. cesareni@uniroma2.it.ORCID http://orcid.org/0000-0002-9528-6018
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Repurposing of drugs for new therapeutic use has received considerable attention for its potential to limit time and cost of drug development. Here we present a new strategy to identify chemicals that are likely to promote a desired phenotype. We used data from the Connectivity Map (CMap) to produce a ranked list of drugs according to their potential to activate transcription factors that mediate myeloid differentiation of leukemic progenitor cells. To validate our strategy, we tested the in vitro differentiation potential of candidate compounds using the HL-60 human cell line as a myeloid differentiation model. Ten out of 22 compounds, which were ranked high in the inferred list, were confirmed to promote significant differentiation of HL-60. These compounds may be considered candidate for differentiation therapy. The method that we have developed is versatile and it can be adapted to different drug repurposing projects.

Identifiers

PMID35013135
PMCPMC8748454
OpenAlexW4225820477

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.