Evidence map›Paper›PMID 41163575›Full record

ArticleHaematologica2026

TGFβ-activated kinase-1 knockdown in hematopoietic stem-progenitor cells causes PANoptosis and myelodysplastic syndrome-like disease in mice.

Lei Zhang, Wenyan Li, Rohit Thalla, Rongyao Ma, Ryan Mack, Ameet R Kini, Austin Runde, Patrick A Hagen, Kevin Barton, Jorgena Kosti-Schwartz and 3 more

Abstract read
In one paragraph

Article in Haematologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. 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

13 authors.

Lei ZhangCyrus Tang Hematology Center, Collaborative Innovation Center of Hematology, National Clinical Research Center for Hematologic Diseases, MOE Engineering Center of Hematological Disease, Soochow University, Suzhou 215123, China; Oncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Wenyan LiLanzhou University Second Hospital, Key Laboratory of Urological Diseases in Gansu Province, Lanzhou, Gansu 730030.
Rohit ThallaOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Rongyao MaCyrus Tang Hematology Center, Collaborative Innovation Center of Hematology, National Clinical Research Center for Hematologic Diseases, MOE Engineering Center of Hematological Disease, Soochow University, Suzhou 215123.
Ryan MackOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Ameet R KiniDepartments of Pathology and Radiation Oncology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Austin RundeOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Patrick A HagenOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Medicine, Loyola University Chicago Medical Center, Maywood, IL 60153.
Kevin BartonOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Medicine, Loyola University Chicago Medical Center, Maywood, IL 60153.
Jorgena Kosti-SchwartzOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Departments of Pathology and Radiation Oncology, Loyola University Chicago Medical Center, Maywood, IL 60153.
Peter BreslinOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Departments of Biology and Molecular/Cellular Physiology, Loyola University Chicago, Maywood, IL 60153.
Hong-Long JiDepartment of Surgery, Loyola University Chicago Medical Center, Maywood, IL 60153.
Jiwang ZhangOncology Institute, Cardinal Bernardin Cancer Canter, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Department of Cancer Biology, Loyola University Chicago Medical Center, Maywood, IL 60153, USA; Departments of Pathology and Radiation Oncology, Loyola University Chicago Medical Center, Maywood, IL 60153. jzhang@luc.edu.

Funding

RIP1/RIP3-Calpain-Stat3 and NF-kappa B pathways in AML pathogenesis and treatmentR01CA223194 · NCI · LOYOLA UNIVERSITY CHICAGO · PI ZHANG, JIWANG · 2018 to 2022
$1.7M
Systematic identification of hematopoietic stem cell expansion factorsR01HL133560 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI ZHANG, JIWANG · 2017 to 2020
$1.5M
Targeting PANoptotic pathways for Myelodysplastic Syndromes treatmentR01CA301049 · NCI · LOYOLA UNIVERSITY CHICAGO · PI Jiwang Zhang · 2025 to 2026
$688k
NCI NIH HHS R01 CA223194NCI NIH HHS R01 CA301049NHLBI NIH HHS R01 HL133560
6 · The paper itself

Abstract

Mutant SF3B1 (SF3B1mut) in hematopoietic stem/progenitor cells (HSPC) primarily affects erythropoiesis, resulting in myelodysplastic syndromes (MDS) with refractory macrocytic anemia and ring sideroblasts. SF3B1mut results in aberrant splicing of a large number of transcripts in HSPC due to the alternative use of cryptic splice sites. Aberrant splicing of Tmem14c and Abcb7 has been shown to be the cause of the ring sideroblasts. However, the key mis-spliced gene(s) that drive macrocytic anemia have not been well-determined. Mis-splicing and downregulation of TAK1 pre-mRNA was detected in SF3B- 1mut-HSPC. We found that TAK1 is required for the survival of HSPC by restricting RIPK1-dependent and -independent PANoptosis. PANoptosis was increased in bone marrow samples from SF3B1mut-MDS patients. To study whether TAK1-downregulation is the cause of anemia in SF3B1mut-MDS, we knocked down Tak1 (Tak1KD) in mouse HSPC. We found that mice transplanted with Tak1KD-HSPC developed anemia and that Ripk1 inhibition could restore blood cell counts in such anemic mice. Tak1KD-HSPC are highly sensitive to TAK1 inhibitor- or cIAP inhibitor-induced PANoptosis. Furthermore, RIPK1 inhibition could also correct differentiation and survival defects of SF3B1mut human erythroblasts. TAK1 inhibitor could also preferentially eliminate SF3B1mut HSPC from MDS patient samples. Our study suggests that SF3B1mut MDS can be treated by either inhibition of RIPK1-PANoptotic signaling to restore blood cell counts or activation of PANoptosis to eliminate the mutant HSPC.

Indexed as

Hematopoietic Stem CellsMAP Kinase Kinase KinasesMyelodysplastic SyndromesRNA Splicing FactorsAnimalsDisease Models, AnimalErythropoiesisGene Knockdown TechniquesHumansMiceMutationPhosphoproteinsMAP Kinase Kinase KinasesPhosphoproteinsRNA Splicing FactorsSF3B1 protein, humanSf3b1 protein, mouse

Identifiers

PMID41163575
PMCPMC13040159

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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.