Evidence map›Paper›PMID 42122191›Full record

ArticleCancers2026

Development and Characterization of a Novel Congenital Acute Erythroid Leukemia Cell Line with Unique Features.

Prasiksha Sitaula, Manisha Gadgeel, Holly Edwards, Lisa Polin, Juiwanna Kushner, Sijana H Dzinic, Kathryn White, Yubin Ge, Jeffrey W Taub, Katherine Gurdziel and 6 more

Abstract read
In one paragraph

Article in Cancers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Prasiksha SitaulaDivision of Hematology/Oncology, Children's Hospital of Michigan, Detroit, MI 48201, USA.ORCID 0009-0007-7470-486X
Manisha GadgeelDivision of Hematology/Oncology, Flow Cytometry Laboratory, Children's Hospital of Michigan, Detroit, MI 48201, USA.ORCID 0000-0001-8366-9487
Holly EdwardsDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Lisa PolinDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Juiwanna KushnerDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Sijana H DzinicDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Kathryn WhiteDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Yubin GeDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.ORCID 0000-0002-8748-716X
Jeffrey W TaubDivision of Hematology/Oncology, Children's Hospital of Michigan, Detroit, MI 48201, USA.ORCID 0000-0003-2228-3235
Katherine GurdzielGenome Sciences Core, Department of Pharmacology and IEHS, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0002-3784-072X
Hunter DlugasDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.ORCID 0000-0002-6819-0045
Greg DysonDepartment of Oncology, Wayne State University School of Medicine, Detroit, MI 48201, USA.ORCID 0000-0001-9783-8464
Rozzelle ArleneDivision of Plastic and Reconstructive Surgery, Children's Hospital of Michigan, Detroit, MI 48201, USA.
David CarrDepartment of Pathology, Detroit Medical Center, Wayne State University, Detroit, MI 48201, USA.ORCID 0000-0003-2559-8902
Omar MoussaDepartment of Pathology, Detroit Medical Center, Wayne State University, Detroit, MI 48201, USA.
Süreyya SavaşanDivision of Hematology/Oncology, Children's Hospital of Michigan, Detroit, MI 48201, USA.ORCID 0000-0001-7138-3027

Funding

Children's Foundation R1-2021-41
6 · The paper itself

Abstract

backgroundAcute erythroid leukemia (AEL) or AML-M6 predominantly affects older adults and is rare in childhood. Compared with other AML subtypes, AEL remains relatively understudied because of its rarity. We established LS-CHM, a novel AEL cell line derived from the ascitic fluid of a patient with congenital leukemia. Interestingly, leukemic cells persisted in the ascitic fluid even after successful eradication from the bone marrow and extramedullary sites.

methodLeukemia cells from the ascites fluid exhibited robust proliferation in culture independent of cytokine requirement and were further characterized by flow cytometric immunophenotyping, cytogenetics, cell cycle and doubling time analysis, colony formation, genome and RNA sequencing, myeloid gene next generation sequencing, and cytotoxicity analysis.

resultsLS-CHM displayed CD36, partial CD235a, CD31, CD43, and CD71 expression and demonstrated in vitro robust growth and high sensitivity to chemotherapeutic agents. A PDX mouse model showed development of leukemia. Genomic analysis revealed a frameshift

conclusionsLS-CHM represents the first congenital AEL-derived cell line, in contrast to the predominantly adult-origin and often secondary erythroid leukemia cell lines available currently. Thus, LS-CHM provides a unique pediatric and extramedullary AEL model, expanding the existing spectrum of AEL cell lines and offering valuable opportunities for biologic and therapeutic investigations.

Indexed as

acute erythroid leukemiaascitic fluidcell linecongenital leukemiaextramedullary disease

Identifiers

PMID42122191
PMCPMC13162582

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Registered trials

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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.