Evidence map›Paper›PMID 35815408›Full record

ArticleCancer biology & therapy2022

Clinical activity of 9-ING-41, a small molecule selective glycogen synthase kinase-3 beta (GSK-3β) inhibitor, in refractory adult T-Cell leukemia/lymphoma.

Andrew Hsu, Kelsey E Huntington, Andre De Souza, Lanlan Zhou, Adam J Olszewski, Nirav P Makwana, Diana O Treaba, Ludimila Cavalcante, Francis J Giles, Howard Safran and 2 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Cancer biology & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. The cross-talk between GSK-3β, RKIP, and PTEN as potential targets for therapeutic implications in cancer: a comprehensive insight.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
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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

12 authors at 1 institution in 1 country.

Andrew HsuDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.
Kelsey E HuntingtonLegorreta Cancer Center at Brown University, The Warren Alpert Medical School, Brown University, Providence, RI, USA.
Andre De SouzaDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.
Lanlan ZhouLegorreta Cancer Center at Brown University, The Warren Alpert Medical School, Brown University, Providence, RI, USA.
Adam J OlszewskiDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.
Nirav P MakwanaDepartment of Radiology, The Warren Alpert Medical School, Brown University, Providence, RI, USA.
Diana O TreabaDepartment of Pathology and Laboratory Medicine, The Warren Alpert Medical School, Brown University, Providence, RI, USA.
Ludimila CavalcanteActuate Therapeutics, Fort Worth, Tx, USA.
Francis J GilesActuate Therapeutics, Fort Worth, Tx, USA.
Howard SafranDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.
Wafik S El-DeiryDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.
Benedito A CarneiroDivision of Hematology/Oncology, Brown University and the Lifespan Cancer Institute, Providence, RI, USA.ORCID 0000-0002-5468-1126
Brown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GSK-3β is a serine/threonine kinase implicated in tumorigenesis and chemotherapy resistance. GSK-3β blockade downregulates the NF-κB pathway, modulates immune cell PD-1 and tumor cell PD-L1 expression, and increases CD8 + T cell and NK cell function. We report a case of adult T-cell leukemia/lymphoma (ATLL) treated with 9-ING-41, a selective GSK-3β inhibitor in clinical development, who achieved a durable response. A 43-year-old male developed diffuse lymphadenopathy, and biopsy of axillary lymph node showed acute-type ATLL. Peripheral blood flow cytometry revealed a circulating clonal T cell population, and CSF was positive for ATLL involvement. After disease progression on the 3

Indexed as

Leukemia-Lymphoma, Adult T-CellLymphomaAdultApoptosisGlycogen Synthase Kinase 3 betaHumansMaleNF-kappa BProtein Kinase InhibitorsGlycogen Synthase Kinase 3 betaNF-kappa BProtein Kinase Inhibitors9-ING-41ATLLglycogen synthase kinase 3GSK-3GSK-3b

Identifiers

PMID35815408
PMCPMC9272832
OpenAlexW4284971983

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.