Evidence map›Paper›PMID 31205227›Full record

ArticleMelanoma research2020

Evolutionarily conserved resistance to phagocytosis observed in melanoma cells is insensitive to upregulation of pro-phagocytic signals and to CD47 blockade.

Katie L Anderson, Kristin M Snyder, Daisuke Ito, Debra C Lins, Lauren J Mills, Kipp Weiskopf, Nan G Ring, Aaron M Ring, Yoji Shimizu, Matthew F Mescher and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Melanoma research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Recent advances in the regulation of CD47 by non-coding RNAs and its therapeutic potential in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. Review
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  4. Targeting HDAC6 improves anti-CD47 immunotherapy.Journal of experimental & clinical cancer research : CR · 2024
    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

12 authors at 7 institutions in 5 countries.

Katie L AndersonDVM/PhD dual degree program of the Comparative Molecular Biosciences Graduate Group.
Kristin M SnyderAnimal Cancer Care and Research Program.
Daisuke ItoAnimal Cancer Care and Research Program.
Debra C LinsDepartments of Laboratory Medicine and Pathology.
Lauren J MillsAnimal Cancer Care and Research Program.
Kipp WeiskopfInstitute for Stem Cell Biology and Regenerative Medicine.
Nan G RingInstitute for Stem Cell Biology and Regenerative Medicine.
Aaron M RingInstitute for Stem Cell Biology and Regenerative Medicine.
Yoji ShimizuMasonic Cancer Center.
Matthew F MescherMasonic Cancer Center.
Irving L WeissmanInstitute for Stem Cell Biology and Regenerative Medicine.
Jaime F ModianoAnimal Cancer Care and Research Program.
Institute for Stem Cell Biology and Regenerative Medicine · INBreast Cancer Care · GBMasonic Cancer CenterBristol-Myers Squibb (Japan) · JPDana-Farber Cancer Institute · USInstitute of Immunology · HRMinnesota Supercomputing Institute

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
Type I interferons in tolerance in the steady stateP01AI035296 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MUELLER, DANIEL L · 1993 to 2023
$31.1M
therapeutic Targeting of CD47 on Human Leukemia and Other Cancer Stem CellsP01CA139490 · NCI · STANFORD UNIVERSITY · PI CLARKE, MICHAEL · 2009 to 2013
$8.7M
Stem Cell Biology, Cancer Stem Cell Biology, and Cancer ImmunotherapyR35CA220434 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2017 to 2023
$6.7M
Sensitization to CD47 Blockade to Enhance Anti-Tumor ImmunityF30CA195973 · NCI · UNIVERSITY OF MINNESOTA · PI ANDERSON, KATIE LYNNE · 2015 to 2018
$177k
NCI NIH HHS F30 CA195973NCI NIH HHS P01 CA139490NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA077598NCI NIH HHS R35 CA220434NIAID NIH HHS P01 AI035296
6 · The paper itself

Abstract

Therapeutic activation of macrophage phagocytosis has the ability to restrain tumour growth through phagocytic clearance of tumour cells and activation of the adaptive immune response. Our objective for this study was to evaluate the effects of modulating pro- and anti-phagocytic pathways in malignant melanoma. In order to identify evolutionarily conserved mechanisms of resistance that may be important for melanoma cell survival, we utilized a multi-species approach and examined the phagocytosis of human, mouse, and dog melanoma cells. We observed that melanoma cells from all three species displayed unexpected resistance to phagocytosis that could not be fully mitigated by blockade of the 'don't eat me' signal CD47 or by chemotherapeutic enhancement of known 'eat me' signals. Additionally, CD47 blockade failed to promote anti-melanoma immune responses or tumour regression in vivo. This melanoma resistance to phagocytosis was not mediated by soluble factors, and it was unaffected by siRNA-mediated knockdown of 47 prospective 'don't eat me' signals or by CRISPR-Cas-mediated CD47 knockout. Unexpectedly, CD47 knockout also did not enhance phagocytosis of lymphoma cells, but it eliminated the pro-phagocytic effect of CD47 blockade, suggesting that the pro-phagocytic effects of CD47 blockade are due in part to Fc receptor engagement. From this study, we conclude that melanoma cells possess an evolutionarily conserved resistance to macrophage phagocytosis. Further investigation will be needed to overcome the mechanisms that mediate melanoma cell resistance to innate immunity.

Indexed as

AnimalsCD47 AntigenCell Line, TumorHumansMelanomaMicePhagocytosisSignal TransductionTransfectionUp-RegulationCD47 AntigenCD47 protein, human

Identifiers

PMID31205227
PMCPMC6906263
OpenAlexW2950132225

What OpenQuestion holds

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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.