Evidence map›Paper›PMID 37143728›Full record

ArticleFrontiers in endocrinology2023

A functional genetic screen for metabolic proteins unveils GART and the

Manuela Cipolletti, Stefano Leone, Stefania Bartoloni, Filippo Acconcia

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Manuela CipollettiDepartment of Sciences, Section Biomedical Sciences, and Technology, University Roma Tre, Rome, Italy.
Stefano LeoneDepartment of Sciences, Section Biomedical Sciences, and Technology, University Roma Tre, Rome, Italy.
Stefania BartoloniDepartment of Sciences, Section Biomedical Sciences, and Technology, University Roma Tre, Rome, Italy.
Filippo AcconciaDepartment of Sciences, Section Biomedical Sciences, and Technology, University Roma Tre, Rome, Italy.
Roma Tre University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting tumor cell metabolism is a new frontier in cancer management. Thus, metabolic pathway inhibitors could be used as anti-estrogen receptor α (ERα) breast cancer (BC) drugs. Here, the interplay among metabolic enzyme(s), the ERα levels and cell proliferation was studied. siRNA-based screen directed against different metabolic proteins in MCF10a, MCF-7 and MCF-7 cells genetically resistant to endocrine therapy (ET) drugs and metabolomic analyses in numerous BC cell lines unveil that the inhibition of GART, a key enzyme in the purine

Indexed as

Breast NeoplasmsCarbon-Nitrogen LigasesCarcinoma, Ductal, BreastBiosynthetic PathwaysEstrogen Receptor alphaFemaleHumansNeoplasm Recurrence, LocalPhosphoribosylglycinamide FormyltransferasePurinesCarbon-Nitrogen LigasesEstrogen Receptor alphaGART protein, humanPhosphoribosylglycinamide FormyltransferasePurines17β-estradiolbreast cancerde novo purine biosynthetic pathwayestrogen receptor αGARTlometrexolmetabolic reprogramming

Identifiers

PMID37143728
PMCPMC10151738
OpenAlexW4366290726

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.