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Updated: Nov 3, 2025

Dual Effects of Melanoma Cell-derived Factors on Bone Marrow Adipocytes Differentiation
Published on: August 23, 2018
Melanoma Cell State-Specific Responses to TNFα.
Su Yin Lim1,2, Sara Alavi2,3, Zizhen Ming1,2
1Department of Biomedical Sciences, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW 2109, Australia.
Tumor necrosis factor alpha (TNFα) signaling impacts melanoma cells, influencing their response to immunotherapy. While TNFα doesn't boost antigen presentation, it increases immune checkpoints, potentially driving resistance to programmed cell death protein 1 (PD1) inhibitors.
Area of Science:
- Oncology
- Immunology
- Dermatology
Background:
- Immune checkpoint inhibitors targeting the programmed cell death protein 1 (PD1) pathway have transformed advanced melanoma treatment.
- Tumor necrosis factor alpha (TNFα), a product of T cell activation, has complex roles in melanoma response and resistance to PD1 inhibitors.
Purpose of the Study:
- To investigate the effect of TNFα on melanoma dedifferentiation, antigen presentation, and immune inhibition.
- To understand how TNFα signaling influences melanoma cell behavior in the context of immunotherapy.
Main Methods:
- Analysis of TNFα signaling in a panel of 40 melanoma cell lines.
- Assessment of TNFα's impact on melanoma dedifferentiation markers.
- Evaluation of TNFα's effect on antigen presentation molecules (HLA-ABC, HLA-DR) and immune checkpoint ligand (PD-L2) expression.
Main Results:
- TNFα signaling is present in all tested melanomas.
- The downstream effects of TNFα depend on the differentiation status of melanoma cells.
- TNFα poorly induces HLA-ABC and HLA-DR but effectively induces PD-L2 expression in melanoma cells.
Conclusions:
- TNFα induces changes in melanoma cells that may contribute to resistance against immunotherapy.
- Targeting TNFα or its downstream effects could be a strategy to overcome immunotherapy resistance in melanoma.
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