Bright-Field Multiplex Immunohistochemistry Assay for Tumor Microenvironment Evaluation in Melanoma Tissues.

bright-field multiplex immunohistochemistry melanoma tumor microenvironment

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
28 Jul 2022
Historique:
received: 20 06 2022
revised: 20 07 2022
accepted: 26 07 2022
entrez: 12 8 2022
pubmed: 13 8 2022
medline: 13 8 2022
Statut: epublish

Résumé

The tumor microenvironment (TME) plays a crucial role in melanoma development, progression and response to treatment. As many of the most relevant TME cell phenotypes are defined by the simultaneous detection of more than two markers, the bright-field (BF) multiplex immunohistochemistry (IHC) technique has been introduced for the quantitative assessment and evaluation of the relative spatial distances between immune cells and melanoma cells. In the current study, we aimed to validate BF multiplex IHC techniques in the Ventana Discovery Ultra Immunostainer to be applied to the evaluation of the TME in variably pigmented melanoma tissues. The BF multiplex IHC staining was performed using different combinations of six immune-cell markers-CD3, CD4, CD8, CD20, CD68 and CD163-and the melanoma cell marker SOX10. Our results show that the BF double IHC Yellow/Purple protocol guarantees the maximum contrast in all the cell populations tested and the combination SOX10 (Green), CD8 (Yellow) and CD163 (Purple) of the BF triple IHC protocol ensures the best contrast and discrimination between the three stained cell populations. Furthermore, the labeled cells were clearly distinct and easily identifiable using the image analysis software. Our standardized BF IHC multiplex protocols can be used to better assess the immune contexts of melanoma patients with potential applications to drive therapeutic decisions within clinical trials.

Identifiants

pubmed: 35954345
pii: cancers14153682
doi: 10.3390/cancers14153682
pmc: PMC9367593
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Fondazione AIRC "Programma di ricerca 5 per Mille 2018"
ID : ID#21073

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Auteurs

Filippo Ugolini (F)

Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy.

Elisa Pasqualini (E)

Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy.

Sara Simi (S)

Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy.

Gianna Baroni (G)

Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy.

Daniela Massi (D)

Section of Pathological Anatomy, Department of Health Sciences, University of Florence, 50139 Florence, Italy.

Classifications MeSH