Evidence map›Paper›PMID 30112706›Full record

ReviewCurrent hematologic malignancy reports2018

Emerging EZH2 Inhibitors and Their Application in Lymphoma.

Jennifer K Lue, Jennifer E Amengual

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hematologic malignancy reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 98 citations in OpenAlex.

  1. Pooled it
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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

2 authors at 1 institution in 1 country.

Jennifer K LueCenter for Lymphoid Malignancies, Department of Medicine, Columbia University Medical Center, 51 W 51st Street, Suite 200, New York, NY, 10019, USA.
Jennifer E AmengualCenter for Lymphoid Malignancies, Department of Medicine, Columbia University Medical Center, 51 W 51st Street, Suite 200, New York, NY, 10019, USA. jea2149@columbia.edu.
Columbia University Irving Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewEnhancer of Zeste Homolog 2 (EZH2) is histone methyltransferase and catalyzes the methylation of histone 3 lysine 27, a mark of transcriptional repression. Various studies have elucidated the complex role of EZH2 in both normal biology and tumorigenesis. Here, we critically review the emerging role of EZH2 in malignancies, the development of small molecule inhibitors of EZH2, and their application in lymphoma. RECENT

findingsActivating mutations and overexpression of EZH2 are found in non-Hodgkin lymphoma (NHL). As a result, several EZH2 inhibitors have been developed and entered clinical investigation. Tazemetostat, first-in-class EZH2 inhibitor, demonstrated enhanced clinical activity in mutant follicular lymphoma and diffuse large B cell lymphoma. With the early activity noted by tazemetostat in B cell lymphomas, the role of EZH2 inhibition in NHL is becoming more evident. This can be leveraged in future rationale combinations to enhance the activity of EZH2 inhibitors.

Indexed as

Enhancer of Zeste Homolog 2 ProteinLymphoma, FollicularLymphoma, Large B-Cell, DiffuseNeoplasm ProteinsAnimalsAntineoplastic AgentsBenzamidesBiphenyl CompoundsEnzyme InhibitorsHumansMorpholinesPyridonesAntineoplastic AgentsBenzamidesBiphenyl CompoundsEnhancer of Zeste Homolog 2 ProteinEnzyme InhibitorsEZH2 protein, humanMorpholinesNeoplasm ProteinsPyridonestazemetostatEpigeneticsEZH2EZH2 inhibitorsHistone methylationNon-Hodgkin lymphoma

Identifiers

PMID30112706
OpenAlexW2887768610

What OpenQuestion holds

Textmetadata
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.