Evidence map›Paper›PMID 28484265›Full record

ArticleLeukemia2017

JAK/STAT pathway inhibition overcomes IL7-induced glucocorticoid resistance in a subset of human T-cell acute lymphoblastic leukemias.

C Delgado-Martin, L K Meyer, B J Huang, K A Shimano, M S Zinter, J V Nguyen, G A Smith, J Taunton, S S Winter, J R Roderick and 5 more

3 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in Leukemia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
12.2field-weighted citation impact, top 1% 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.

NCT04582604 phase1 / phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Ruxolitinib and Decitabine Intensified Conditioning Regimen for Patients With High Risk Hematological Malignancies Underwenting Allogeneic Stem Cell Transplantation

TypeinterventionalSponsorChinese PLA General HospitalRan2020 to 2025Enrolled60ConditionsPeripheral Blood Stem Cell TransplantationArmsmodified By/Cy conditioning regimen intensified by Ruxolitinib and Decitabine
NCT05075681 phase1 / phase2unknown statusnot on this mapstarted 2021, after this paper: background citation

Ruxolitinib and Chidamide Intensified Bu/CY Conditioning Regimen for Patients With Acute T Cell Lymphoblast Leukemia/ Lymphoblastic Lymphoma Underwenting Haploidenticl Peripheral Blood Stem Cell Transplantation

TypeinterventionalSponsorChinese PLA General HospitalRan2021 to 2025Enrolled50ConditionsPeripheral Blood Stem Cell TransplantationArmsModified By/Cy conditioning regimen intensified by Ruxolitinib and Chidamide
NCT05088226 phase2recruitingnot on this mapstarted 2021, after this paper: background citation

Ruxolitinib and Chidamide Intensified Bu/CY Conditioning Regimen for Patients With Acute B Cell Lymphoblast Leukemia Underwenting Haploidenticl Peripheral Blood Stem Cell Transplantation

TypeinterventionalSponsorChinese PLA General HospitalRan2021 to 2031Enrolled50ConditionsPeripheral Blood Stem Cell TransplantationArmsRuxolitinib combined with Chidamide.
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 128 citations in OpenAlex.

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  5. Robust CD4medRxiv : the preprint server for health sciences · 2025
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  16. Development of constitutively synergistic nanoformulations to enhance chemosensitivity in T-cell leukemia.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
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  18. Article
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17 more citing papers are in PubMed but not listed here.

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 8 institutions in 1 country.

C Delgado-MartinDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
L K MeyerDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
B J HuangDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
K A ShimanoDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
M S ZinterDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
J V NguyenDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
G A SmithHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
J TauntonHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
S S WinterDepartment of Pediatric Hematology/Oncology, University of New Mexico, Albuquerque, NM, USA.
J R RoderickDepartment of Cancer Biology, University of Massachusetts, Worcester, MA, USA.
M A KelliherDepartment of Cancer Biology, University of Massachusetts, Worcester, MA, USA.
T M HortonDepartment of Pediatrics, Texas Children's Hospital, Houston, TX, USA.
B L WoodDepartment of Laboratory Medicine, University of Washington, Seattle, WA, USA.
D T TeacheyDepartment of Pediatrics, Children's Hospital of Pennsylvania, Philadelphia, PA, USA.
M L HermistonDepartment of Pediatrics, University of California, San Francisco, Benioff Children's Hospital, San Francisco, CA, USA.
UCSF Benioff Children's Hospital · USUniversity of California, San Francisco · USUniversity of Massachusetts Chan Medical School · USChildren's Hospital of Philadelphia · USTexas Children's Hospital · USUCSF Helen Diller Family Comprehensive Cancer Center · USUniversity of New Mexico · USUniversity of Washington · US

Funding

RESEARCH TRAINING IN CHEMISTRY AND CHEMICAL BIOLOGYT32GM064337 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CRAIK, CHARLES SCOTT · 2002 to 2021
$7.8M
Mechanism(s) of TAL-1/SCL-mediated LeukemogenesisR01CA096899 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MICHELLE ALICE KELLIHER · 2004 to 2026
$6.9M
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
Research Training in Childhood CancerT32CA128583 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Alejandro Sweet-Cordero · 2007 to 2026
$6.0M
NCI NIH HHS R01 CA096899NCI NIH HHS R01 CA193776NCI NIH HHS T32 CA128583NIGMS NIH HHS T32 GM064337
6 · The paper itself

Abstract

While outcomes for children with T-cell acute lymphoblastic leukemia (T-ALL) have improved dramatically, survival rates for patients with relapsed/refractory disease remain dismal. Prior studies indicate that glucocorticoid (GC) resistance is more common than resistance to other chemotherapies at relapse. In addition, failure to clear peripheral blasts during a prednisone prophase correlates with an elevated risk of relapse in newly diagnosed patients. Here we show that intrinsic GC resistance is present at diagnosis in early thymic precursor (ETP) T-ALLs as well as in a subset of non-ETP T-ALLs. GC-resistant non-ETP T-ALLs are characterized by strong induction of JAK/STAT signaling in response to interleukin-7 (IL7) stimulation. Removing IL7 or inhibiting JAK/STAT signaling sensitizes these T-ALLs, and a subset of ETP T-ALLs, to GCs. The combination of the GC dexamethasone and the JAK1/2 inhibitor ruxolitinib altered the balance between pro- and anti-apoptotic factors in samples with IL7-dependent GC resistance, but not in samples with IL7-independent GC resistance. Together, these data suggest that the addition of ruxolitinib or other inhibitors of IL7 receptor/JAK/STAT signaling may enhance the efficacy of GCs in a biologically defined subset of T-ALL.

Indexed as

Drug Resistance, NeoplasmAnimalsAntineoplastic AgentsBcl-2-Like Protein 11Cell Line, TumorDexamethasoneDisease Models, AnimalGlucocorticoidsHumansInterleukin-7Janus Kinase InhibitorsJanus KinasesMicePrecursor T-Cell Lymphoblastic Leukemia-LymphomaProto-Oncogene Proteins c-bcl-2Signal TransductionAntineoplastic AgentsBcl-2-Like Protein 11DexamethasoneGlucocorticoidsInterleukin-7Janus Kinase InhibitorsJanus KinasesProto-Oncogene Proteins c-bcl-2STAT Transcription Factors

Identifiers

PMID28484265
PMCPMC5729333
OpenAlexW2612483493

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.