Evidence map›Paper›PMID 31417180›Full record

ArticleOncogene2019

T-cell acute lymphoblastic leukemia displays autocrine production of Interleukin-7.

Anne Buffière, Benjamin Uzan, Romain Aucagne, François Hermetet, Manon Mas, Sandra Nassurdine, Aziza Aznague, Virginie Carmignac, Benjamin Tournier, Olivier Bouchot and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. The Important Role of Interleukin-2 in COVID-19.Journal of immunology research · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

16 authors.

Anne BuffièreUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Benjamin UzanUMR967, Inserm/CEA/Université Paris 7/Université Paris 11, Fontenay-aux-Roses, France.
Romain AucagneUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
François HermetetUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Manon MasUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Sandra NassurdineUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Aziza AznagueUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Virginie CarmignacUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Benjamin TournierHôpital Universitaire François Mitterrand, Service de Génétique des Cancers, Dijon, France.
Olivier BouchotHôpital Universitaire François Mitterrand, Chirurgie Cardiovasculaire, Dijon, France.
Paola BalleriniAssistance Publique-Hôpitaux de Paris, Laboratoire d'Hématologie, Hôpital Trousseau, Paris, France.
João T BarataInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal.ORCID http://orcid.org/0000-0002-4826-8976
Jean-Noël BastieUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Laurent DelvaUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France.
Françoise PflumioUMR967, Inserm/CEA/Université Paris 7/Université Paris 11, Fontenay-aux-Roses, France.
Ronan QuéréUMR1231, Inserm/Université Bourgogne Franche-Comté, Dijon, France. ronan.quere@inserm.fr.ORCID http://orcid.org/0000-0002-1615-6769

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy characterized by an accumulation of immature T cells. Although patient outcomes have improved, novel targeted therapies are needed to reduce the intensity of chemotherapy and improve the prognosis of high-risk patients. Interleukin-7 (IL-7) modulates the survival and proliferation of normal and malignant T cells. Targeting the IL-7 signaling pathway is thus a potentially effective therapeutic strategy. To achieve such aim, it is essential to first understand how the IL-7 signaling pathway is activated. Although IL-7 production has been observed from multiple stromal tissues, T-ALL autocrine IL-7 secretion has not yet been described. Interestingly, using T-ALL cell lines, primary and patient-derived xenotransplanted (PDX) T-ALL cells, we demonstrate that T-ALL cells produce IL-7 whereas normal T cells do not. Finally, using knock down of IL7 gene in T-ALL cells, we describe to what extent IL-7 autocrine secretion is involved in the T-ALL cells propagation in bone marrow and how it affects the number of leukemia-initiating cells in PDX mice. Together, these results demonstrate how the autocrine production of the IL-7 cytokine mediated by T-ALL cells can be involved in the oncogenic development of T-ALL and offer novel insights into T-ALL spreading.

Indexed as

Autocrine CommunicationAnimalsApoptosisBone MarrowCell ProliferationFemaleHumansInterleukin-7MaleMiceMice, Inbred NODMice, SCIDPrecursor T-Cell Lymphoblastic Leukemia-LymphomaT-LymphocytesTumor Cells, CulturedXenograft Model Antitumor AssaysIL7 protein, humanInterleukin-7

Identifiers

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.