Evidence map›Paper›PMID 35163302›Full record

ArticleInternational journal of molecular sciences2022

Histamine H4 Receptor Agonism Induces Antitumor Effects in Human T-Cell Lymphoma.

Mariángeles Clauzure, Mónica A Táquez Delgado, Jude M Phillip, Maria V Revuelta, Leandro Cerchietti, Vanina A Medina

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Mast Cells and Basophils in IgE-Independent Anaphylaxis.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Molecular Biology of Histamine System, Volume 1.International journal of molecular sciences · 2022
    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

6 authors at 3 institutions in 2 countries.

Mariángeles ClauzureLaboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), National Scientific and Technical Research Council (CONICET), Buenos Aires 1107, Argentina.
Mónica A Táquez DelgadoLaboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), National Scientific and Technical Research Council (CONICET), Buenos Aires 1107, Argentina.
Jude M PhillipHematology and Oncology Division, Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
Maria V RevueltaHematology and Oncology Division, Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
Leandro CerchiettiHematology and Oncology Division, Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
Vanina A MedinaLaboratory of Tumor Biology and Inflammation, Institute for Biomedical Research (BIOMED), School of Medical Sciences, Pontifical Catholic University of Argentina (UCA), National Scientific and Technical Research Council (CONICET), Buenos Aires 1107, Argentina.
Cornell University · USConsejo Nacional de Investigaciones Científicas y Técnicas · ARPontificia Universidad Católica Argentina · AR

Funding

Agencia Nacional de Promoción Científica y Tecnológica PICT2018-03778National Scientific and Technical Research Council 1508PCB
6 · The paper itself

Abstract

The discovery of the human histamine H4 receptor (H4R) has contributed to our understanding of the role of histamine in numerous physiological and pathological conditions, including tumor development and progression. The lymph nodes of patients with malignant lymphomas have shown to contain high levels of histamine, however, less is known regarding the expression and function of the H4R in T-cell lymphoma (TCL). In this work we demonstrate the expression of H4R isoforms (mRNA and protein) in three human aggressive TCL (OCI-Ly12, Karpas 299, and HuT78). Histamine and specific H4R agonists (VUF8430 and JNJ28610244) significantly reduced cell viability in a dose-dependent manner (

Indexed as

Antineoplastic AgentsApoptosisCell LineCell Line, TumorCell ProliferationHEK293 CellsHistamineHistamine AgonistsHistamine AntagonistsHumansLymphoma, T-CellOxidative StressReceptors, Histamine H4Antineoplastic AgentsHistamineHistamine AgonistsHistamine AntagonistsHRH4 protein, humanReceptors, Histamine H4apoptosisH4R isoformshistaminepanobinostatproliferationT-cell lymphoma

Identifiers

PMID35163302
PMCPMC8836034
OpenAlexW4210796701

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.