Evidence map›Paper›PMID 35008680›Full record

ReviewInternational journal of molecular sciences2021

Histone Modifications and Their Targeting in Lymphoid Malignancies.

Miranda Fernández-Serrano, René Winkler, Juliana C Santos, Marguerite-Marie Le Pannérer, Marcus Buschbeck, Gaël Roué

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Acetylation of Histone H3 in Cancer Progression and Prognosis.International journal of molecular sciences · 2024
    Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
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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

6 authors at 2 institutions in 1 country.

Miranda Fernández-SerranoLymphoma Translational Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0001-9040-8496
René WinklerChromatin, Metabolism and Cell Fate Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0002-7570-0242
Juliana C SantosLymphoma Translational Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0003-4148-9570
Marguerite-Marie Le PannérerChromatin, Metabolism and Cell Fate Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0002-5779-8805
Marcus BuschbeckChromatin, Metabolism and Cell Fate Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0002-3218-4567
Gaël RouéLymphoma Translational Group, Josep Carreras Leukaemia Research Institute (IJC), 08916 Badalona, Spain.ORCID 0000-0003-0245-2257
Josep Carreras Leukaemia Research Institute · ESUniversitat Autònoma de Barcelona · ES

Funding

Agency for Administration of University and Research 2017-SGR-305Deutsche José Carreras Leukämie Stiftung DJCLS 14R/2018Instituto de Salud Carlos III PI18/01383La Marató de TV3 257/C/2019Marie Skłodowska Curie Training network H2020-MSCA-ITN-2020-953407Ministerio de Ciencia e Innovación RTI2018-094005-B-I00
6 · The paper itself

Abstract

In a wide range of lymphoid neoplasms, the process of malignant transformation is associated with somatic mutations in B cells that affect the epigenetic machinery. Consequential alterations in histone modifications contribute to disease-specific changes in the transcriptional program. Affected genes commonly play important roles in cell cycle regulation, apoptosis-inducing signal transduction, and DNA damage response, thus facilitating the emergence of malignant traits that impair immune surveillance and favor the emergence of different B-cell lymphoma subtypes. In the last two decades, the field has made a major effort to develop therapies that target these epigenetic alterations. In this review, we discuss which epigenetic alterations occur in B-cell non-Hodgkin lymphoma. Furthermore, we aim to present in a close to comprehensive manner the current state-of-the-art in the preclinical and clinical development of epigenetic drugs. We focus on therapeutic strategies interfering with histone methylation and acetylation as these are most advanced in being deployed from the bench-to-bedside and have the greatest potential to improve the prognosis of lymphoma patients.

Indexed as

Protein Processing, Post-TranslationalClinical Trials as TopicEpigenesis, GeneticHistonesHumansLymphomaModels, BiologicalHistonesbromodomain inhibitorsclinical testingDNA methylationdrug combinationepigeneticsEZH2HATHDACnon-Hodgkin lymphoma

Identifiers

PMID35008680
PMCPMC8745418
OpenAlexW4226023587

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.