Evidence map›Paper›PMID 38321096›Full record

ArticleScientific reports2024

Investigation of the potential effects of estrogen receptor modulators on immune checkpoint molecules.

Nikita Abramenko, Fréderic Vellieux, Kateřina Veselá, Zdeněk Kejík, Jan Hajduch, Michal Masařík, Petr Babula, David Hoskovec, Karel Pacák, Pavel Martásek and 2 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Research progress in estrogen as an adjunctive therapy for schizophrenia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
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.

Nikita AbramenkoBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Fréderic VellieuxBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Kateřina VeseláBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Zdeněk KejíkBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Jan HajduchBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Michal MasaříkBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Petr BabulaDepartment of Physiology, Faculty of Medicine, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
David Hoskovec1st Department of Surgery-Department of Abdominal, Thoracic Surgery and Traumatology, First Faculty of Medicine, Charles University and General University Hospital, U Nemocnice 2, 121 08, Prague, Czech Republic.
Karel PacákSection on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Building 10, Room 1-3140, 10 Center Drive, Bethesda, MD, 20892, USA.
Pavel MartásekDepartment of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital, 120 00, Prague, Czech Republic.
Karel SmetanaBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic.
Milan JakubekBIOCEV, First Faculty of Medicine, Charles University, 252 50, Vestec, Czech Republic. Milan.Jakubek@lf1.cuni.cz.

Funding

Charles University SVV260637; SVV260521; UNCE 204064; Progres LF1 Q38 and Q27, Cooperatio ONCOEuropean- Union LX22NPO5102 and LX22NPO5107Ministry of Education, Youth, and Sports . LM2023053Technology Agency of the Czech Republic TN02000109the Ministry of Health NU22-D-136 and NU21-08-00407
6 · The paper itself

Abstract

Immune checkpoints regulate the immune system response. Recent studies suggest that flavonoids, known as phytoestrogens, may inhibit the PD-1/PD-L1 axis. We explored the potential of estrogens and 17 Selective Estrogen Receptor Modulators (SERMs) as inhibiting ligands for immune checkpoint proteins (CTLA-4, PD-L1, PD-1, and CD80). Our docking studies revealed strong binding energy values for quinestrol, quercetin, and bazedoxifene, indicating their potential to inhibit PD-1 and CTLA-4. Quercetin and bazedoxifene, known to modulate EGFR and IL-6R alongside estrogen receptors, can influence the immune checkpoint functionality. We discuss the impact of SERMs on PD-1 and CTLA-4, suggesting that these SERMs could have therapeutic effects through immune checkpoint inhibition. This study highlights the potential of SERMs as inhibitory ligands for immune checkpoint proteins, emphasizing the importance of considering PD-1 and CTLA-4 inhibition when evaluating SERMs as therapeutic agents. Our findings open new avenues for cancer immunotherapy by exploring the interaction between various SERMs and immune checkpoint pathways.

Indexed as

Immune Checkpoint ProteinsNeoplasmsB7-H1 AntigenCTLA-4 AntigenEstrogen Receptor ModulatorsHumansImmunotherapyProgrammed Cell Death 1 ReceptorQuercetinSelective Estrogen Receptor ModulatorsB7-H1 AntigenCTLA-4 AntigenEstrogen Receptor ModulatorsImmune Checkpoint ProteinsProgrammed Cell Death 1 ReceptorQuercetinSelective Estrogen Receptor Modulators

Identifiers

PMID38321096
PMCPMC10847107

What OpenQuestion holds

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LicenceCC BY
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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.