In Vitro Three-Dimensional (3D) Models for Melanoma Immunotherapy

Author:

Nomdedeu-Sancho Gemma1ORCID,Gorkun Anastasiya1,Mahajan Naresh1,Willson Kelsey1,Schaaf Cecilia R.123,Votanopoulos Konstantinos I.1245,Atala Anthony12ORCID,Soker Shay1246

Affiliation:

1. Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, Winston Salem, NC 27101, USA

2. Wake Forest Organoid Research Center (WFORCE), Winston-Salem, NC 27101, USA

3. Pathology Section, Comparative Medicine, Wake Forest University School of Medicine, Winston Salem, NC 27101, USA

4. Department of Cancer Biology, Wake Forest University School of Medicine, Winston Salem, NC 27101, USA

5. Department of Surgery, Division of Surgical Oncology, Wake Forest Baptist Health, Winston Salem, NC 27157, USA

6. Medical Center Boulevard, Winston-Salem, NC 27157, USA

Abstract

Melanoma is responsible for the majority of skin cancer-related fatalities. Immune checkpoint inhibitor (ICI) treatments have revolutionized the management of the disease by significantly increasing patient survival rates. However, a considerable number of tumors treated with these drugs fail to respond or may develop resistance over time. Tumor growth and its response to therapies are critically influenced by the tumor microenvironment (TME); it directly supports cancer cell growth and influences the behavior of surrounding immune cells, which can become tumor-permissive, thereby rendering immunotherapies ineffective. Ex vivo modeling of melanomas and their response to treatment could significantly advance our understanding and predictions of therapy outcomes. Efforts have been directed toward developing reliable models that accurately mimic melanoma in its appropriate tissue environment, including tumor organoids, bioprinted tissue constructs, and microfluidic devices. However, incorporating and modeling the melanoma TME and immune component remains a significant challenge. Here, we review recent literature regarding the generation of in vitro 3D models of normal skin and melanoma and the approaches used to incorporate the immune compartment in such models. We discuss how these constructs could be combined and used to test immunotherapies and elucidate treatment resistance mechanisms. The development of 3D in vitro melanoma models that faithfully replicate the complexity of the TME and its interaction with the immune system will provide us with the technical tools to better understand ICI resistance and increase its efficacy, thereby improving personalized melanoma therapy.

Funder

Wake Forest Institute for Regenerative Medicine

Wake Forest Comprehensive Cancer Center

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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