Evidence map›Paper›PMID 24362524›Full record

ArticleOncogene2014

Chromatin-associated CSF-1R binds to the promoter of proliferation-related genes in breast cancer cells.

V Barbetti, A Morandi, I Tusa, G Digiacomo, M Riverso, I Marzi, M G Cipolleschi, S Bessi, A Giannini, A Di Leo and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  6. Potential Stereoselective Binding ofMolecules (Basel, Switzerland) · 2022
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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 2 institutions in 1 country.

V BarbettiDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
A MorandiDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
I TusaDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
G DigiacomoDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
M RiversoDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
I MarziDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
M G CipolleschiDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
S BessiAnatomia Patologica, Ospedale di Prato, Prato, Italy.
A GianniniAnatomia Patologica, Ospedale di Prato, Prato, Italy.
A Di Leo8216;Sandro Pitigliani' Medical Oncology Unit, Department of Oncology, Hospital of Prato, IstitutoToscanoTumori, Prato, Italy.
P Dello SbarbaDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
E RovidaDipartimento di Scienze Biomediche, Sperimentali e Cliniche, Sezione di Patologia, Universitá degli Studi di Firenze, Istituto Toscano Tumori, Firenze, Italy.
University of Florence · ITNuovo Ospedale di Prato · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The colony-stimulating factor-1 (CSF-1) and its receptor CSF-1R physiologically regulate the monocyte/macrophage system, trophoblast implantation and breast development. An abnormal CSF-1R expression has been documented in several human epithelial tumors, including breast carcinomas. We recently demonstrated that CSF-1/CSF-1R signaling drives proliferation of breast cancer cells via 'classical' receptor tyrosine kinase signaling, including activation of the extracellular signal-regulated kinase 1/2. In this paper, we show that CSF-1R can also localize within the nucleus of breast cancer cells, either cell lines or tissue specimens, irrespectively of their intrinsic molecular subtype. We found that the majority of nuclear CSF-1R is located in the chromatin-bound subcellular compartment. Chromatin immunoprecipitation revealed that CSF-1R, once in the nucleus, binds to the promoters of the proliferation-related genes CCND1, c-JUN and c-MYC. CSF-1R also binds the promoter of its ligand CSF-1 and positively regulates CSF-1 expression. The existence of such a receptor/ligand regulatory loop is a novel aspect of CSF-1R signaling. Moreover, our results provided the first evidence of a novel localization site of CSF-1R in breast cancer cells, suggesting that CSF-1R could act as a transcriptional regulator on proliferation-related genes.

Indexed as

Cell ProliferationPromoter Regions, GeneticAnimalsBase SequenceBreast NeoplasmsCell Line, TumorCell NucleusChromatinFeedback, PhysiologicalFemaleGene Expression Regulation, NeoplasticHumansMiceNIH 3T3 CellsProtein BindingProtein TransportChromatinReceptor, Macrophage Colony-Stimulating Factor

Identifiers

PMID24362524
PMCPMC4141303
OpenAlexW2061049252

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.