Evidence map›Paper›PMID 37370739›Full record

ArticleCancers2023

GTN Enhances Antitumor Effects of Doxorubicin in TNBC by Targeting the Immunosuppressive Activity of PMN-MDSC.

Nesrine Mabrouk, Cindy Racoeur, Jingxuan Shan, Aurélie Massot, Silvia Ghione, Malorie Privat, Lucile Dondaine, Elise Ballot, Caroline Truntzer, Romain Boidot and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 11 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

18 authors at 5 institutions in 2 countries.

Nesrine MabroukLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Cindy RacoeurLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Jingxuan ShanGenetic Intelligence Laboratory, Weill Cornell Medicine-Qatar, Qatar Foundation, Doha P.O. Box 24144, Qatar.
Aurélie MassotLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Silvia GhioneLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Malorie PrivatLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Lucile DondaineLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Elise BallotPlateforme de Transfert en Biologie Cancérologique, Centre GFL Leclerc, 21000 Dijon, France.
Caroline TruntzerPlateforme de Transfert en Biologie Cancérologique, Centre GFL Leclerc, 21000 Dijon, France.ORCID 0000-0003-0895-4813
Romain BoidotUnit of Molecular Biology, Georges-François Leclerc Cancer Center-UNICANCER, CNRS UMR 6302, 21000 Dijon, France.ORCID 0000-0001-9956-1737
François HermetetCRI UMR INSERM1231, 21000 Dijon, France.ORCID 0000-0001-5549-1992
Valentin DerangèrePlateforme de Transfert en Biologie Cancérologique, Centre GFL Leclerc, 21000 Dijon, France.
Mélanie BruchardCRI UMR INSERM1231, 21000 Dijon, France.
Frédérique VégranPlateforme de Transfert en Biologie Cancérologique, Centre GFL Leclerc, 21000 Dijon, France.ORCID 0000-0002-4377-1441
Lotfi ChouchaneGenetic Intelligence Laboratory, Weill Cornell Medicine-Qatar, Qatar Foundation, Doha P.O. Box 24144, Qatar.
François GhiringhelliPlateforme de Transfert en Biologie Cancérologique, Centre GFL Leclerc, 21000 Dijon, France.ORCID 0000-0002-5465-8305
Ali BettaiebLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.
Catherine PaulLaboratoire d'Immunologie et Immunothérapie des Cancers, EPHE, PSL Research University, 75006 Paris, France.ORCID 0000-0002-7657-5535
École Pratique des Hautes Études · FRInserm · FRCentre Georges François Leclerc · FRWeill Cornell Medical College in Qatar · QACentre National de la Recherche Scientifique · FR

Funding

Ligue contre le Cancer CCIR-GE 2016Qatar National Research Fund NPRP9-459-3-090
6 · The paper itself

Abstract

(1) Background: Immunosuppression is a key barrier to effective anti-cancer therapies, particularly in triple-negative breast cancer (TNBC), an aggressive and difficult to treat form of breast cancer. We investigated here whether the combination of doxorubicin, a standard chemotherapy in TNBC with glyceryltrinitrate (GTN), a nitric oxide (NO) donor, could overcome chemotherapy resistance and highlight the mechanisms involved in a mouse model of TNBC. (2) Methods: Balb/C-bearing subcutaneous 4T1 (TNBC) tumors were treated with doxorubicin (8 mg/Kg) and GTN (5 mg/kg) and monitored for tumor growth and tumor-infiltrating immune cells. The effect of treatments on MDSCs reprogramming was investigated ex vivo and in vitro. (3) Results: GTN improved the anti-tumor efficacy of doxorubicin in TNBC tumors. This combination increases the intra-tumor recruitment and activation of CD8

Indexed as

doxorubicinglyceryl trinitrateimmunotherapynitric oxide donorPMN-MDSCtriple-negative breast cancer

Identifiers

PMID37370739
PMCPMC10296121
OpenAlexW4380088358

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.