Inter-Tumor Heterogeneity-Melanomas Respond Differently to GM-CSF-Mediated Activation.
Animals
Astrocytes
/ drug effects
Brain
/ pathology
Cell Line, Tumor
Cellular Microenvironment
/ drug effects
Endothelial Cells
/ drug effects
Granulocyte-Macrophage Colony-Stimulating Factor
/ pharmacology
Humans
Interleukin-1alpha
/ metabolism
Male
Melanoma
/ pathology
Mice, Inbred BALB C
Mice, Nude
Skin Neoplasms
/ pathology
Solubility
Transendothelial and Transepithelial Migration
/ drug effects
Tumor Necrosis Factor-alpha
/ metabolism
GM-CSF
brain metastasis
melanoma
metastatic microenvironment
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
13 07 2020
13 07 2020
Historique:
received:
01
07
2020
revised:
09
07
2020
accepted:
10
07
2020
entrez:
17
7
2020
pubmed:
17
7
2020
medline:
5
3
2021
Statut:
epublish
Résumé
Granulocyte-monocyte colony stimulating factor (GM-CSF) is used as an adjuvant in various clinical and preclinical studies with contradictory results. These were attributed to opposing effects of GM-CSF on the immune or myeloid systems of the treated patients or to lack of optimal dosing regimens. The results of the present study point to inter-tumor heterogeneity as a possible mechanism accounting for the contrasting responses to GM-CSF incorporating therapies. Employing xenograft models of human melanomas in nude mice developed in our lab, we detected differential functional responses of melanomas from different patients to GM-CSF both in vitro as well as in vivo. Whereas cells of one melanoma acquired pro metastatic features following exposure to GM-CSF, cells from another melanoma either did not respond or became less malignant. We propose that inter-melanoma heterogeneity as manifested by differential responses of melanoma cells (and perhaps also of other tumor) to GM-CSF may be developed into a predictive marker providing a tool to segregate melanoma patients who will benefit from GM-CSF therapy from those who will not.
Identifiants
pubmed: 32668704
pii: cells9071683
doi: 10.3390/cells9071683
pmc: PMC7407964
pii:
doi:
Substances chimiques
Interleukin-1alpha
0
Tumor Necrosis Factor-alpha
0
Granulocyte-Macrophage Colony-Stimulating Factor
83869-56-1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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