Evidence map›Paper›PMID 35434798›Full record

ArticleBritish journal of haematology2022

Inhibition of the Sec61 translocon overcomes cytokine-induced glucocorticoid resistance in T-cell acute lymphoblastic leukaemia.

Lauren K Meyer, Cristina Delgado-Martin, Phillip P Sharp, Benjamin J Huang, Dustin McMinn, Tiffaney L Vincent, Theresa Ryan, Terzah M Horton, Brent L Wood, David T Teachey and 3 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. HighOpen medicine (Warsaw, Poland) · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. 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

13 authors at 4 institutions in 1 country.

Lauren K MeyerDepartment of Pediatrics, University of California, San Francisco, California, USA.ORCID 0000-0002-7603-8457
Cristina Delgado-MartinDepartment of Pediatrics, University of California, San Francisco, California, USA.
Phillip P SharpDepartment of Cellular and Molecular Pharmacology, University of California, San Francisco, California, USA.
Benjamin J HuangDepartment of Pediatrics, University of California, San Francisco, California, USA.
Dustin McMinnKezar Life Sciences, South San Francisco, California, USA.
Tiffaney L VincentChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Theresa RyanChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Terzah M HortonTexas Children's Hospital, Houston, Texas, USA.
Brent L WoodChildren's Hospital Los Angeles, Los Angeles, California, USA.
David T TeacheyChildren's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Jack TauntonDepartment of Cellular and Molecular Pharmacology, University of California, San Francisco, California, USA.
Christopher J KirkKezar Life Sciences, South San Francisco, California, USA.
Michelle L HermistonDepartment of Pediatrics, University of California, San Francisco, California, USA.ORCID 0000-0003-1790-2679
University of California, San Francisco · USChildren's Hospital of Philadelphia · USChildren's Hospital of Los Angeles · USTexas Children's Hospital · US

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alan Ashworth · 1999 to 2026
$209.7M
Medical Scientist Training Program (T32 NRSA Training Grant)T32GM141323 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Aimee Kao · 2021 to 2026
$10.5M
Improving risk allocation and developing novel therapies for children with T-ALL and T-LLR01CA193776 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI Terzah M Horton, ADAM B OLSHEN · 2015 to 2026
$6.2M
NCI NIH HHS P30 CA082103NCI NIH HHS R01 CA193776NIGMS NIH HHS T32 GM141323
6 · The paper itself

Abstract

Glucocorticoid (GC) resistance is a poor prognostic factor in T-cell acute lymphoblastic leukaemia (T-ALL). Interleukin-7 (IL-7) mediates GC resistance via GC-induced upregulation of IL-7 receptor (IL-7R) expression, leading to increased pro-survival signalling. IL-7R reaches the cell surface via the secretory pathway, so we hypothesized that inhibiting the translocation of IL-7R into the secretory pathway would overcome GC resistance. Sec61 is an endoplasmic reticulum (ER) channel that is required for insertion of polypeptides into the ER. Here, we demonstrate that KZR-445, a novel inhibitor of Sec61, potently attenuates the dexamethasone (DEX)-induced increase in cell surface IL-7R and overcomes IL-7-induced DEX resistance.

Indexed as

Precursor T-Cell Lymphoblastic Leukemia-LymphomaSEC Translocation ChannelsCytokinesDexamethasoneGlucocorticoidsHumansInterleukin-7Metabolism, Inborn ErrorsReceptors, GlucocorticoidT-LymphocytesCytokinesDexamethasoneGlucocorticoidsInterleukin-7Receptors, GlucocorticoidSEC Translocation ChannelscytokineglucocorticoidsSec61 inhibitorT-cell acute lymphoblastic leukaemia

Identifiers

PMID35434798
PMCPMC9322670
OpenAlexW4224130815

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.