Evidence map›Paper›PMID 30944118›Full record

ArticleCancer discovery2019

Cytokine-Regulated Phosphorylation and Activation of TET2 by JAK2 in Hematopoiesis.

Jong Jin Jeong, Xiaorong Gu, Ji Nie, Sriram Sundaravel, Hui Liu, Wen-Liang Kuo, Tushar D Bhagat, Kith Pradhan, John Cao, Sangeeta Nischal and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer discovery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
5.6field-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

40 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  10. Article
  11. Review
  12. Review
  13. Clonal hematopoiesis and bone marrow inflammation.Translational research : the journal of laboratory and clinical medicine · 2023
    Review
  14. Review
  15. Article
  16. Role of TET dioxygenases in the regulation of both normal and pathological hematopoiesis.Journal of experimental & clinical cancer research : CR · 2022
    Review
  17. Article
  18. Article
  19. Article
  20. Mechanisms that regulate the activities of TET proteins.Cellular and molecular life sciences : CMLS · 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

26 authors at 8 institutions in 1 country.

Jong Jin JeongSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Xiaorong GuCleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
Ji NieDepartment of Chemistry, The University of Chicago, Chicago, Illinois.
Sriram SundaravelSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Hui LiuSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Wen-Liang KuoSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Tushar D BhagatAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.ORCID 0000-0002-4527-5505
Kith PradhanAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
John CaoSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Sangeeta NischalAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
Kathy L McGrawMoffitt Cancer Center, Tampa, Florida.
Sanchari BhattacharyyaAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
Michael R BishopSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Andrew ArtzSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Michael J ThirmanSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Alison MoliternoDepartment of Hematology, Johns Hopkins School of Medicine, Baltimore, Maryland.ORCID 0000-0002-8673-4317
Peng JiDepartment of Pathology, Northwestern University, Chicago, Illinois.
Ross L LevineMemorial Sloan Kettering Cancer Center, New York, New York.
Lucy A GodleySection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois.
Ulrich SteidlAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
James J BiekerDepartment of Cell, Developmental and Regenerative Biology, Mount Sinai School of Medicine, New York, New York.
Alan F ListMoffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-1647-2972
Yogen SaunthararajahCleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.ORCID 0000-0002-9757-1031
Chuan HeDepartment of Chemistry, The University of Chicago, Chicago, Illinois.
Amit VermaAlbert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York. awickrema@uchicago.edu amit.verma@einstein.yu.edu.
Amittha WickremaSection of Hematology/Oncology, Department of Medicine, The University of Chicago, Chicago, Illinois. awickrema@uchicago.edu amit.verma@einstein.yu.edu.
University of Chicago · USAlbert Einstein College of Medicine · USCleveland Clinic · USMoffitt Cancer Center · USIcahn School of Medicine at Mount Sinai · USJohns Hopkins University · USMemorial Sloan Kettering Cancer Center · USNorthwestern University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Mechanisms of Formation and Progression of Preleukemic Stem CellsR01CA217092 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STEIDL, ULRICH · 2017 to 2021
$2.0M
Leveraging epigenetic and epitranscriptomic aberrations in cancer to identify molecular targets for designing therapyK00CA223044 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SUNDARAVEL, SRIRAM · 2019 to 2022
$379k
Leveraging epigenetic and epitranscriptomic aberrations in cancer to identify molecular targets for designing therapyF99CA223044 · NCI · UNIVERSITY OF CHICAGO · PI SUNDARAVEL, SRIRAM · 2017 to 2018
$90k
NCI NIH HHS F99 CA223044NCI NIH HHS K00 CA223044NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA217092
6 · The paper itself

Abstract

Even though the Ten-eleven translocation (TET) enzymes catalyze the generation of 5-hydroxymethylcytosines required for lineage commitment and subsequent differentiation of stem cells into erythroid cells, the mechanisms that link extracellular signals to TET activation and DNA hydroxymethylation are unknown. We demonstrate that hematopoietic cytokines phosphorylate TET2, leading to its activation in erythroid progenitors. Specifically, cytokine receptor-associated JAK2 phosphorylates TET2 at tyrosines 1939 and 1964. Phosphorylated TET2 interacts with the erythroid transcription factor KLF1, and this interaction with TET2 is increased upon exposure to erythropoietin. The activating JAK2

Indexed as

Transcriptional ActivationBiomarkersCytokinesDioxygenasesDNA-Binding ProteinsHematopoiesisHematopoietic Stem CellsHumansJanus Kinase 2PhosphorylationProto-Oncogene ProteinsBiomarkersCytokinesDioxygenasesDNA-Binding ProteinsJAK2 protein, humanJanus Kinase 2Proto-Oncogene ProteinsTET2 protein, human

Identifiers

PMID30944118
PMCPMC6697164
OpenAlexW2929105074

What OpenQuestion 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 OpenQuestion graph.