Inter-Tumor Heterogeneity-Melanomas Respond Differently to GM-CSF-Mediated Activation.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
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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Auteurs

Adi Moshe (A)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.
Department of Immunology, Weizmann Institute of Science, Rehovot 7610001, Israel.

Sivan Izraely (S)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

Orit Sagi-Assif (O)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

Sapir Malka (S)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

Shlomit Ben-Menachem (S)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

Tsipi Meshel (T)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

Metsada Pasmanik-Chor (M)

Bioinformatics Unit, The George S. Wise Faculty of Life Science, Tel Aviv University, Tel-Aviv 6997801, Israel.

Dave S B Hoon (DSB)

Department of Translational Molecular Medicine, John Wayne Cancer Institute, Saint John's Health Center Providence Health Systems, Santa Monica, CA 90404, USA.

Isaac P Witz (IP)

School of Molecular Cell Biology and Biotechnology, George S. Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 6997801, Israel.

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Classifications MeSH