Evidence map›Paper›PMID 28864529›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Thyroid hormone receptor beta and NCOA4 regulate terminal erythrocyte differentiation.

Xiaofei Gao, Hsiang-Ying Lee, Wenbo Li, Randall Jeffrey Platt, M Inmaculada Barrasa, Qi Ma, Russell R Elmes, Michael G Rosenfeld, Harvey F Lodish

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 11% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  8. Article
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  11. Myxedema Coma-associated Pancytopenia: A Case Report.Rambam Maimonides medical journal · 2024
    Article
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  16. Article
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  19. Article
  20. Role of Nuclear Receptors in Controlling Erythropoiesis.International journal of molecular sciences · 2022
    Review
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

9 authors at 5 institutions in 1 country.

Xiaofei GaoWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Hsiang-Ying LeeWhitehead Institute for Biomedical Research, Cambridge, MA 02142.ORCID 0000-0002-1503-5818
Wenbo LiHoward Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093.
Randall Jeffrey PlattDepartment of Biological Engineering, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139.
M Inmaculada BarrasaWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Qi MaDepartment of Medicine, School of Medicine, University of California, San Diego, La Jolla, CA 92093.
Russell R ElmesWhitehead Institute for Biomedical Research, Cambridge, MA 02142.
Michael G RosenfeldHoward Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093.
Harvey F LodishWhitehead Institute for Biomedical Research, Cambridge, MA 02142; lodish@wi.mit.edu.
Whitehead Institute for Biomedical Research · USHoward Hughes Medical Institute · USUniversity of California San Diego · USBroad Institute · USIIT@MIT · US

Funding

TRANSCRIPTION FACTOR GATA-1 IN TERMINAL ERYTHROID DEVELOPMENTP01HL032262 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ORKIN, STUART H · 1985 to 2021
$38.9M
REGULATION OF NEUROENDOCRINE SWITCHING EVENTSR37DK039949 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ROSENFELD, MICHAEL G · 1987 to 2020
$12.3M
Howard Hughes Medical InstituteNHLBI NIH HHS P01 HL032262NIDDK NIH HHS R37 DK039949
6 · The paper itself

Abstract

An effect of thyroid hormone (TH) on erythropoiesis has been known for more than a century but the molecular mechanism(s) by which TH affects red cell formation is still elusive. Here we demonstrate an essential role of TH during terminal human erythroid cell differentiation; specific depletion of TH from the culture medium completely blocked terminal erythroid differentiation and enucleation. Treatment with TRβ agonists stimulated premature erythroblast differentiation in vivo and alleviated anemic symptoms in a chronic anemia mouse model by regulating erythroid gene expression. To identify factors that cooperate with TRβ during human erythroid terminal differentiation, we conducted RNA-seq in human reticulocytes and identified nuclear receptor coactivator 4 (NCOA4) as a critical regulator of terminal differentiation. Furthermore,

Indexed as

Cell DifferentiationAnimalsChromatinGenome-Wide Association StudyHumansMiceMice, KnockoutNuclear Receptor CoactivatorsReticulocytesThyroid Hormone Receptors betaThyroid HormonesChromatinNCOA4 protein, humanNcoA4 protein, mouseNuclear Receptor CoactivatorsThyroid Hormone Receptors betaThyroid HormoneserythropoiesisNCOA4nuclear receptorthyroid hormone

Identifiers

PMID28864529
PMCPMC5617304
OpenAlexW2753783443

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.