Evidence map›Paper›PMID 25351294›Full record

ReviewAnnals of the New York Academy of Sciences2015

Notch signaling in the malignant bone marrow microenvironment: implications for a niche-based model of oncogenesis.

Andrew G Evans, Laura M Calvi

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Metabolomics of healthy hematopoietic stem cells and leukemic stem cells.Journal of clinical and translational research · 2025
    Article
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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

2 authors at 1 institution in 1 country.

Andrew G EvansHematopathology Unit, Department of Pathology, University of Rochester School of Medicine and Dentistry, Rochester, New York.
Laura M Calvi
University of Rochester · US

Funding

Universiity of Rochester Center for Medical Countermeasures against RadiationU19AI091036 · NIAID · UNIVERSITY OF ROCHESTER · PI FINKELSTEIN, JACOB N · 2010 to 2014
$15.6M
The University of Rochester's Clinical and Translational Science InstituteUL1TR000042 · NCATS · UNIVERSITY OF ROCHESTER · PI BENNETT, NANCY M, KIEBURTZ, KARL D. · 2012 to 2015
$14.4M
PGE2 mitigation of acute and late radiation injuryU01AI107276 · NIAID · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M, PALIS, JAMES · 2013 to 2017
$2.9M
Regulatory Cell Signals in the Bone MarrowR01DK081843 · NIDDK · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M · 2009 to 2013
$1.8M
Therapeutic Targeting of Leukemia-Microenvironmental InteractionsR01CA166280 · NCI · UNIVERSITY OF ROCHESTER · PI BECKER, MICHAEL W, CALVI, LAURA M · 2013 to 2017
$1.6M
Hematopoietic-Osteoblastic InteractionsR01DK076876 · NIDDK · UNIVERSITY OF ROCHESTER · PI CALVI, LAURA M · 2008 to 2012
$1.5M
Modulation of aged hematopoietic stem cell nichesR01AG046293 · NIA · UNIVERSITY OF ROCHESTER · PI BECKER, MICHAEL W, CALVI, LAURA M · 2013 to 2017
$954k
NCI NIH HHS CA166280NCI NIH HHS R01 CA166280NIAID NIH HHS AI091036NIAID NIH HHS AI107276NIAID NIH HHS U01 AI107276NIAID NIH HHS U19 AI091036NIA NIH HHS AG046293NIA NIH HHS R01 AG046293NIDDK NIH HHS DK081843NIDDK NIH HHS R01 DK076876NIDDK NIH HHS R01 DK081843
6 · The paper itself

Abstract

Fueled by the growing interest in stem cell biology and the promise of regenerative medicine, study of the hematopoietic stem cell (HSC) microenvironment has provided critical insights into normal and malignant hematopoiesis. Notch receptor signaling in this microenvironment is a critical regulator of HSC fate and differentiation. Notch signaling also has the potential to modulate the growth of various malignant cell types, as evidenced by the growing list of hematologic cancers and other malignancies associated with either mutations in Notch genes or alterations in Notch signaling. In both health and disease, activation of Notch signaling predominantly exerts influence through stromal cell interactions with the tumor or stem cell microenvironments. Definitive evidence from transgenic mouse models has shown that alterations in stromal cell signaling from the bone marrow niche can induce malignant outgrowth of preleukemic clones and leukemia. Understanding how Notch receptor signals in the bone marrow microenvironment govern stem cell behavior will advance our understanding of cancer pathogenesis in hematologic malignancies and may have implications for treating metastatic solid tumors involving bone. These microenvironmental interactions are potential therapeutic targets for treating and preventing a variety of diseases, including bone marrow failure disorders, myelodysplastic syndromes, leukemia, and lymphoma.

Indexed as

AnimalsBone MarrowBone Marrow NeoplasmsCarcinogenesisCell Transformation, NeoplasticHumansReceptors, NotchSignal TransductionTumor MicroenvironmentReceptors, Notchbone marrowDeltahematopoiesisHSCjaggedleukemiamalignancymicroenvironmentnotchstem cell

Identifiers

PMID25351294
PMCPMC4289406
OpenAlexW1560485785

What OpenQuestion holds

Textmetadata
LicenceTDM
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.