Evidence map›Paper›PMID 23416702›Full record

ArticleNature medicine2013

Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction.

Lihong Shi, Shuaiying Cui, James D Engel, Osamu Tanabe

Abstract read
In one paragraph

Article in Nature medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 166 citations in OpenAlex.

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43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 2 countries.

Lihong ShiDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Shuaiying Cui
James D Engel
Osamu Tanabe
University of Michigan–Ann Arbor · US

Funding

EXPRESSION OF DEVELOPMENTALLY RELATED AVIAN GENESR01HL024415 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ENGEL, JAMES DOUGLAS · 1985 to 2009
$3.3M
Reactivation of Fetal Gamma-globin Genes for the Treatment of Beta-globin DisordeRC1DK086956 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TANABE, OSAMU · 2009 to 2010
$984k
NHLBI NIH HHS HL24415NHLBI NIH HHS R01 HL024415NIDDK NIH HHS DK086956NIDDK NIH HHS RC1 DK086956
6 · The paper itself

Abstract

Enhanced fetal γ-globin synthesis alleviates symptoms of β-globinopathies such as sickle cell disease and β-thalassemia, but current γ-globin-inducing drugs offer limited beneficial effects. We show here that lysine-specific demethylase 1 (LSD1) inhibition by RNAi in human erythroid cells or by the monoamine oxidase inhibitor tranylcypromine in human erythroid cells or β-type globin-transgenic mice enhances γ-globin expression. LSD1 is thus a promising therapeutic target for γ-globin induction, and tranylcypromine may serve as a lead compound for the development of a new γ-globin inducer.

Indexed as

Anemia, Sickle CellAnimalsbeta-Globinsbeta-ThalassemiaCell DifferentiationCells, CulturedErythroid CellsFetal Hemoglobingamma-GlobinsHistone DemethylasesHumansMiceMice, TransgenicMolecular Targeted TherapyMonoamine Oxidase InhibitorsNuclear Receptor Subfamily 2, Group C, Member 1beta-GlobinsFetal Hemoglobingamma-GlobinsHistone DemethylasesKDM1A protein, humanMonoamine Oxidase InhibitorsNR2C2 protein, humanNuclear Receptor Subfamily 2, Group C, Member 1Receptors, SteroidReceptors, Thyroid HormoneRNA, Small InterferingTranylcypromine

Identifiers

PMID23416702
PMCPMC5512162
OpenAlexW2010407535

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.