Evidence map›Paper›PMID 31873722›Full record

ReviewThe Journal of experimental medicine2020

Mapping and targeting of the leukemic microenvironment.

Matthew T Witkowski, Stavroula Kousteni, Iannis Aifantis

Abstract readReview
In one paragraph

Review in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  7. Article
  8. LRG1 Drives AML Progression by Disrupting Myeloid Progenitor Regulation.Blood and lymphatic cancer : targets and therapy · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
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  17. Review
  18. Article
  19. Review
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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.

Matthew T WitkowskiDepartment of Pathology, New York University School of Medicine, New York, NY.
Stavroula KousteniDepartment of Physiology & Cellular Biophysics, Columbia University Irving Medical Center, New York, NY.
Iannis AifantisDepartment of Pathology, New York University School of Medicine, New York, NY.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Mapping cancer micro-environments for acute leukemiaR01CA202025 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS, SCHWAB, SUSAN RUTH · 2016 to 2020
$2.3M
Post-translational control of cancer cell stress response and metastasisR01CA202027 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS, HERNANDO, EVA · 2016 to 2020
$2.3M
Genetic characterization of osteoblast-induced leukemiasR01HL130937 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KOUSTENI, STAVROULA, RABADAN, RAUL · 2016 to 2019
$2.0M
Molecular basis of the inhibitory effects of ATRA on osteoblast-induced MDS/AMLR56AR054447 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KOUSTENI, STAVROULA · 2019 to 2019
$356k
NCI NIH HHS P30 CA013696NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA202025NCI NIH HHS R01 CA202027NHLBI NIH HHS R01 HL130937NIAMS NIH HHS R56 AR054447
6 · The paper itself

Abstract

Numerous studies support a role of the microenvironment in maintenance of the leukemic clone, as well as in treatment resistance. It is clear that disruption of the normal bone marrow microenvironment is sufficient to promote leukemic transformation and survival in both a cell autonomous and non-cell autonomous manner. In this review, we provide a snapshot of the various cell types shown to contribute to the leukemic microenvironment as well as treatment resistance. Several of these studies suggest that leukemic blasts occupy specific cellular and biochemical "niches." Effective dissection of critical leukemic niche components using single-cell approaches has allowed a more precise and extensive characterization of complexity that underpins both the healthy and malignant bone marrow microenvironment. Knowledge gained from these observations can have an important impact in the development of microenvironment-directed targeted approaches aimed at mitigating disease relapse.

Indexed as

Tumor MicroenvironmentAdipocytesAnimalsB-LymphocytesBone MarrowEndothelium, VascularHumansImmunotherapy, AdoptiveLeukemiaMesenchymal Stem CellsMiceOsteoblastsReceptors, Chimeric AntigenSignal TransductionStem Cell NicheT-LymphocytesReceptors, Chimeric Antigen

Identifiers

PMID31873722
PMCPMC7041707

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.