Evidence map›Paper›PMID 35926109›Full record

ReviewBlood2023

Single-cell analysis of acute lymphoblastic and lineage-ambiguous leukemia: approaches and molecular insights.

Ilaria Iacobucci, Matthew T Witkowski, Charles G Mullighan

Open access · bronzeAbstract readReview
In one paragraph

Review in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 30 citations in OpenAlex.

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  12. [Research progress on copy number alterations in pediatric B-cell acute lymphoblastic leukemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
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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

3 authors at 2 institutions in 1 country.

Ilaria IacobucciDepartment of Pathology, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0003-2008-1365
Matthew T WitkowskiDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0003-1434-4288
Charles G MullighanDepartment of Pathology, St Jude Children's Research Hospital, Memphis, TN.ORCID 0000-0002-1871-1850
St. Jude Children's Research Hospital · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Translating genomic discoveries to improved outcomes for high risk acute leukemiaR35CA197695 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Charles G Mullighan · 2017 to 2026
$11.4M
Dissecting the Functional Role of Monocytes in B-cell Acute Lymphoblastic Leukemia SurvivalK22CA258520 · NCI · UNIVERSITY OF COLORADO DENVER · PI WITKOWSKI, MATTHEW · 2022 to 2024
$553k
NCI NIH HHS K22 CA258520NCI NIH HHS R35 CA197695
6 · The paper itself

Abstract

Despite recent progress in identifying the genetic drivers of acute lymphoblastic leukemia (ALL), prognosis remains poor for those individuals who experience disease recurrence. Moreover, acute leukemias of ambiguous lineage lack a biologically informed framework to guide classification and therapy. These needs have driven the adoption of multiple complementary single-cell sequencing approaches to explore key issues in the biology of these leukemias, including cell of origin, developmental hierarchy and ontogeny, and the molecular heterogeneity driving pathogenesis, progression, and therapeutic responsiveness. There are multiple single-cell techniques for profiling a specific modality, including RNA, DNA, chromatin accessibility and methylation; and an expanding range of approaches for simultaneous analysis of multiple modalities. Single-cell sequencing approaches have also enabled characterization of cell-intrinsic and -extrinsic features of ALL biology. In this review we describe these approaches and highlight the extensive heterogeneity that underpins ALL gene expression, cellular differentiation, and clonal architecture throughout disease pathogenesis and treatment resistance. In addition, we discuss the importance of the dynamic interactions that occur between leukemia cells and the nonleukemia microenvironment. We discuss potential opportunities and limitations of single-cell sequencing for the study of ALL biology and treatment responsiveness.

Indexed as

Precursor Cell Lymphoblastic Leukemia-LymphomaAcute DiseaseHumansLymphocytesPrognosisSingle-Cell AnalysisTumor Microenvironment

Identifiers

PMID35926109
PMCPMC10023733
OpenAlexW4289785468

What OpenQuestion holds

Textmetadata
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.