Evidence map›Paper›PMID 28691928›Full record

ArticleThe Journal of clinical investigation2017

Mutations in 5-methylcytosine oxidase TET2 and RhoA cooperatively disrupt T cell homeostasis.

Shengbing Zang, Jia Li, Haiyan Yang, Hongxiang Zeng, Wei Han, Jixiang Zhang, Minjung Lee, Margie Moczygemba, Sevinj Isgandarova, Yaling Yang and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.8field-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

57 citing papers in PubMed, 93 citations in OpenAlex.

  1. Review
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  4. Article
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  6. Review
  7. Article
  8. Review
  9. Review
  10. In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma.Journal of experimental & clinical cancer research : CR · 2024
    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. Review
  16. Review
  17. Article
  18. TargetingCancers · 2022
    Review
  19. Role of TET dioxygenases in the regulation of both normal and pathological hematopoiesis.Journal of experimental & clinical cancer research : CR · 2022
    Review
  20. 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

15 authors at 6 institutions in 2 countries.

Shengbing ZangCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Jia LiCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Haiyan YangDepartment of Lymphoma, Zhejiang Cancer Hospital, Hangzhou, China.
Hongxiang ZengCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Wei HanCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Jixiang ZhangCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Minjung LeeCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Margie MoczygembaCenter for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University, Houston, Texas, USA.
Sevinj IsgandarovaCenter for Infectious and Inflammatory Diseases, Institute of Biosciences and Technology, Texas A&M University, Houston, Texas, USA.
Yaling YangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Yubin ZhouCenter for Translational Cancer Research, Institute of Biosciences and Technology, and.
Anjana RaoDivision of Signaling and Gene Expression, La Jolla Institute for Allergy and Immunology, La Jolla, California, USA.
M James YouDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Deqiang SunCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Yun HuangCenter for Epigenetics and Disease Prevention, Institute of Biosciences and Technology and.
Prevention Institute · USTexas A&M University · USThe University of Texas MD Anderson Cancer Center · USRenmin Hospital of Wuhan University · CNSanford Consortium for Regenerative Medicine · USZhejiang Cancer Hospital · CN

Funding

University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
SIGNAL TRANSDUCTION AND GENE INDUCTION IN T LYMPHOCYTESR01AI040127 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HOGAN, PATRICK, RAO, ANJANA · 1996 to 2025
$13.3M
Genetic Epidemiology of non-Hodgkin LymphomaR01CA200703 · NCI · MAYO CLINIC ROCHESTER · PI CERHAN, JAMES R · 2016 to 2020
$3.3M
MOLECULAR CONTROL OF CALCIUM INFLUX AT THE ER-PLASMA MEMBRANE JUNCTIONSR01GM112003 · NIGMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI ZHOU, YUBIN · 2014 to 2022
$2.7M
Role of TET proteins in myeloid malignanciesR01CA151535 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2012 to 2016
$1.8M
CHARACTERIZATION AND TARGETED THERAPY OF T-ALL DEFICIENT FOR PTEN AND INK4A/ARFR01CA164346 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YOU, M. JAMES · 2012 to 2015
$1.2M
Illumina HiSeq 2500 Sequencing SystemS10OD016262 · OD · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI RAO, ANJANA · 2013 to 2013
$600k
NCI NIH HHS P50 CA100632NCI NIH HHS R01 CA151535NCI NIH HHS R01 CA164346NCI NIH HHS R01 CA200703NIAID NIH HHS R01 AI040127NIGMS NIH HHS R01 GM112003NIH HHS S10 OD016262
6 · The paper itself

Abstract

Angioimmunoblastic T cell lymphoma (AITL) represents a distinct, aggressive form of peripheral T cell lymphoma with a dismal prognosis. Recent exome sequencing in patients with AITL has revealed the frequent coexistence of somatic mutations in the Rho GTPase RhoA (RhoAG17V) and loss-of-function mutations in the 5-methylcytosine oxidase TET2. Here, we have demonstrated that TET2 loss and RhoAG17V expression in mature murine T cells cooperatively cause abnormal CD4+ T cell proliferation and differentiation by perturbing FoxO1 gene expression, phosphorylation, and subcellular localization, an abnormality that is also detected in human primary AITL tumor samples. Reexpression of FoxO1 attenuated aberrant immune responses induced in mouse models adoptively transferred with T cells and bearing genetic lesions in both TET2 and RhoA. Our findings suggest a mutational cooperativity between epigenetic factors and GTPases in adult CD4+ T cells that may account for immunoinflammatory responses associated with AITL patients.

Indexed as

Mutation5-MethylcytosineAnimalsCD4-Positive T-LymphocytesCell CycleCell ProliferationDioxygenasesDNA-Binding ProteinsDNA MethylationEpigenesis, GeneticFemaleGTP PhosphohydrolasesHomeostasisHumansMaleMice5-MethylcytosineDioxygenasesDNA-Binding ProteinsGTP PhosphohydrolasesOxidoreductasesProto-Oncogene ProteinsrhoA GTP-Binding ProteinRHOA protein, humanRhoA protein, mouserho GTP-Binding ProteinsTET2 protein, humanTet2 protein, mouse

Identifiers

PMID28691928
PMCPMC5531410
OpenAlexW2728024715

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.