Evidence map›Paper›PMID 30720426›Full record

ArticleeLife2019

FGF2-FGFR1 signaling regulates release of Leukemia-Protective exosomes from bone marrow stromal cells.

Nathalie Javidi-Sharifi, Jacqueline Martinez, Isabel English, Sunil K Joshi, Renata Scopim-Ribeiro, Shelton K Viola, David K Edwards, Anupriya Agarwal, Claudia Lopez, Danielle Jorgens and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  7. Isolation and Comprehensive Analysis of Cochlear Tissue-Derived Small Extracellular Vesicles.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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  12. A novel intronic circular RNA circFGFR1Journal of translational medicine · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Nathalie Javidi-Sharifi *Knight Cancer Institute, Oregon Health & Science University, Portland, United States.
Jacqueline Martinez *Knight Cancer Institute, Oregon Health & Science University, Portland, United States.
Isabel EnglishKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Sunil K JoshiKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Renata Scopim-RibeiroKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Shelton K ViolaKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
David K EdwardsKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Anupriya AgarwalKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Claudia LopezKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Danielle JorgensKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Jeffrey W TynerKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Brian J DrukerKnight Cancer Institute, Oregon Health & Science University, Portland, United States.
Elie TraerKnight Cancer Institute, Oregon Health & Science University, Portland, United States.ORCID 0000-0001-8844-2345
Oregon Health & Science University · USHoward Hughes Medical Institute · US

Funding

Tumor Intrinsic and Microenvironmental Mechanisms Driving Drug Combination Efficacy and Resistance in AMLU54CA224019 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Anupriya Agarwal · 2017 to 2026
$13.9M
Functional Genomic Discovery of Pathway Targeted and Immune Modulatory Therapeutic Combinations in Hematologic MalignanciesU01CA217862 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DRUKER, BRIAN J, TYNER, JEFFREY WALLACE · 2017 to 2021
$5.3M
Defining the stromal landscape that sustains AML drug resistanceF30CA239335 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JOSHI, SUNIL KUMAR · 2019 to 2022
$187k
FGF2 Signaling as a Clinically Relevant Resistance Mechanism to TKIs in GISTF30CA186477 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JAVIDI-SHARIFI, NATHALIE R · 2014 to 2016
$144k
NCI NIH HHS F30 CA186477NIH HHS 5F30CA186477-03
6 · The paper itself

Abstract

Protective signaling from the leukemia microenvironment leads to leukemia cell persistence, development of resistance, and disease relapse. Here, we demonstrate that fibroblast growth factor 2 (FGF2) from bone marrow stromal cells is secreted in exosomes, which are subsequently endocytosed by leukemia cells, and protect leukemia cells from tyrosine kinase inhibitors (TKIs). Expression of FGF2 and its receptor, FGFR1, are both increased in a subset of stromal cell lines and primary AML stroma; and increased FGF2/FGFR1 signaling is associated with increased exosome secretion. FGFR inhibition (or gene silencing) interrupts stromal autocrine growth and significantly decreases secretion of FGF2-containing exosomes, resulting in less stromal protection of leukemia cells. Likewise, Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).

Indexed as

Signal TransductionAnimalsCells, CulturedCell SurvivalDisease Models, AnimalExosomesFibroblast Growth Factor 2HumansLeukemia, Myeloid, AcuteMesenchymal Stem CellsMiceMice, KnockoutReceptor, Fibroblast Growth Factor, Type 1Fibroblast Growth Factor 2Receptor, Fibroblast Growth Factor, Type 1bone marrow stromacancer biologydrug resistanceexosomesFGF2FGFR1humanhuman biologymedicinemicroenvironmentmouse

Identifiers

PMID30720426
PMCPMC6363389
OpenAlexW2914662982

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.