Evidence map›Paper›PMID 39504332›Full record

ArticlePloS one2024

Identification of small molecule agonists of fetal hemoglobin expression for the treatment of sickle cell disease.

Jian-Ping Yang, Rachel Toughiri, Anshu P Gounder, Dan Scheibe, Matt Petrus, Sarah J Fink, Sebastien Vallee, Jon Kenniston, Nikolaos Papaioannou, Steve Langston and 2 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. 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

12 authors.

Jian-Ping YangTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Rachel ToughiriTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Anshu P GounderTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Dan ScheibeTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Matt PetrusTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Sarah J FinkTakeda Development Center Americas, Inc., Cambridge, Massachusetts, United States of America.ORCID 0000-0003-2990-2625
Sebastien ValleeTakeda Development Center Americas, Inc., Cambridge, Massachusetts, United States of America.
Jon KennistonTakeda Development Center Americas, Inc., Cambridge, Massachusetts, United States of America.
Nikolaos PapaioannouTakeda Development Center Americas, Inc., Cambridge, Massachusetts, United States of America.ORCID 0000-0002-2516-8497
Steve LangstonTakeda Development Center Americas, Inc., Cambridge, Massachusetts, United States of America.
Narender R GavvaTakeda Development Center Americas, Inc., San Diego, California, United States of America.
Shane R HormanTakeda Development Center Americas, Inc., San Diego, California, United States of America.ORCID 0000-0002-4291-2126

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induction of fetal hemoglobin (HbF) has been shown to be a viable therapeutic approach to treating sickle cell disease and potentially other β-hemoglobinopathies. To identify targets and target-modulating small molecules that enhance HbF expression, we engineered a human umbilical-derived erythroid progenitor reporter cell line (HUDEP2_HBG1_HiBiT) by genetically tagging a HiBiT peptide to the carboxyl (C)-terminus of the endogenous HBG1 gene locus, which codes for γ-globin protein, a component of HbF. Employing this reporter cell line, we performed a chemogenomic screen of approximately 5000 compounds annotated with known targets or mechanisms that have achieved clinical stage or approval by the US Food and Drug Administration (FDA). Among them, 10 compounds were confirmed for their ability to induce HbF in the HUDEP2 cell line. These include several known HbF inducers, such as pomalidomide, lenalidomide, decitabine, idoxuridine, and azacytidine, which validate the translational nature of this screening platform. We identified avadomide, autophinib, triciribine, and R574 as novel HbF inducers from these screens. We orthogonally confirmed HbF induction activities of the top hits in both parental HUDEP2 cells as well as in human primary CD34+ hematopoietic stem and progenitor cells (HSPCs). Further, we demonstrated that pomalidomide and avadomide, but not idoxuridine, induced HbF expression through downregulation of several transcriptional repressors such as BCL11A, ZBTB7A, and IKZF1. These studies demonstrate a robust phenotypic screening workflow that can be applied to large-scale small molecule profiling campaigns for the discovery of targets and pathways, as well as novel therapeutics for sickle cell disease and other β-hemoglobinopathies.

Indexed as

Anemia, Sickle CellFetal HemoglobinCell LineErythroid Precursor Cellsgamma-GlobinsHumansRepressor ProteinsSmall Molecule LibrariesFetal Hemoglobingamma-GlobinsRepressor ProteinsSmall Molecule Libraries

Identifiers

PMID39504332
PMCPMC11540224

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Registered trials

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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.