Evidence map›Paper›PMID 31636099›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

Colony-Stimulating Factor 1 Receptor (CSF1R) Activates AKT/mTOR Signaling and Promotes T-Cell Lymphoma Viability.

Carlos Murga-Zamalloa, Delphine C M Rolland, Avery Polk, Ashley Wolfe, Hiran Dewar, Pinki Chowdhury, Ozlem Onder, Rajan Dewar, Noah A Brown, Nathanael G Bailey and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Novel Insights into the Pathogenic Role of CSF1R in Endometriosis.Reproductive sciences (Thousand Oaks, Calif.) · 2026
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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

14 authors at 4 institutions in 1 country.

Carlos Murga-ZamalloaDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan. rywilcox@med.umich.edu carlosmu@med.umich.edu.
Delphine C M RollandDepartment of Laboratory Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.
Avery PolkDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Ashley WolfeDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Hiran DewarDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Pinki ChowdhuryDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Ozlem OnderDepartment of Laboratory Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0003-0850-1216
Rajan DewarDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.
Noah A BrownDepartment of Pathology, University of Michigan, Ann Arbor, Michigan.ORCID 0000-0001-9151-5912
Nathanael G BaileyDepartment of Pathology, University of Pittsburgh, Pittsburgh, Pennsylvania.ORCID 0000-0002-6747-680X
Kedar InamdarDepartment of Pathology, Henry Ford Hospital, Detroit, Michigan.
Megan S LimDepartment of Laboratory Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.
Kojo S J Elenitoba-JohnsonDepartment of Laboratory Sciences, University of Pennsylvania, Philadelphia, Pennsylvania.
Ryan A WilcoxDepartment of Pathology, University of Michigan, Ann Arbor, Michigan. rywilcox@med.umich.edu carlosmu@med.umich.edu.
University of Michigan · USUniversity of Pennsylvania · USHenry Ford Hospital · USUniversity of Pittsburgh · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
THE T-CELL RECEPTOR'S ROLE IN T-CELL LYMPHOMA PATHOGENESISR37CA233476 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILCOX, RYAN A · 2019 to 2025
$2.2M
Wiskott-Aldrich syndrome protein (WASp) signaling in the oncogenesis of T celllymphomasK08CA218460 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MURGA-ZAMALLOA, CARLOS A. · 2017 to 2019
$320k
NCI NIH HHS K08 CA218460NCI NIH HHS P30 CA046592NCI NIH HHS R37 CA233476
6 · The paper itself

Abstract

purposePeripheral T-cell lymphomas are clinically aggressive and usually fatal, as few complete or durable remissions are achieved with currently available therapies. Recent evidence supports a critical role for lymphoma-associated macrophages during T-cell lymphoma progression, but the specific signals involved in the cross-talk between malignant T cells and their microenvironment are poorly understood. Colony-stimulator factor 1 receptor (CSF1R, CD115) is required for the homeostatic survival of tissue-resident macrophages. Interestingly, its aberrant expression has been reported in a subset of tumors. In this article, we evaluated its expression and oncogenic role in T-cell lymphomas. EXPERIMENTAL

designLoss-of-function studies, including pharmacologic inhibition with a clinically available tyrosine kinase inhibitor, pexidartinib, were performed in multiple

resultsWe observed that CSF1R is aberrantly expressed in many T-cell lymphomas, including a significant number of peripheral and cutaneous T-cell lymphomas. Colony-stimulating factor 1 (CSF1), in an autocrine or paracrine-dependent manner, leads to CSF1R autophosphorylation and activation in malignant T cells. Furthermore, CSF1R signaling was associated with significant changes in gene expression and in the phosphoproteome, implicating PI3K/AKT/mTOR in CSF1R-mediated T-cell lymphoma growth. We also demonstrated that inhibition of CSF1R

conclusionsCollectively, these findings implicate CSF1R in T-cell lymphomagenesis and have significant therapeutic implications.

Indexed as

AminopyridinesAnimalsCell Line, TumorGene Expression ProfilingHumansLymphoma, T-Cell, PeripheralMacrophage Colony-Stimulating FactorMacrophagesMiceMice, Inbred NODMice, SCIDProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPyrrolesReceptor, Macrophage Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating FactorAKT1 protein, humanAminopyridinesCSF1 protein, humanCSF1R protein, humanMacrophage Colony-Stimulating FactorMTOR protein, humanpexidartinibProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPyrrolesReceptor, Macrophage Colony-Stimulating FactorReceptors, Granulocyte-Macrophage Colony-Stimulating FactorTOR Serine-Threonine Kinases

Identifiers

PMID31636099
PMCPMC7002219
OpenAlexW2982009257

What OpenQuestion holds

Textmetadata
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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.