PD-L1 expression by tumor cell lines: A predictive marker in melanoma

Exp Dermatol. 2018 Jun;27(6):647-655. doi: 10.1111/exd.13526.

Abstract

Prognostic biomarkers for patients with melanoma after lymph node resection are of clinical relevance and could thus enable the identification of patients who therefore would most benefit from adjuvant treatment. The aim of this work was to determine, using an in vitro model, whether immune-related biomarkers, such as MHC-class I and II, melanoma-associated antigens, IDO1 and PD-L1, could also be relevant to predict the risk of relapse of patients with stage III melanoma after lymph node resection. We established tumor cell lines from metastatic lymph nodes of 50 patients with melanoma. The expression of investigated biomarkers was determined on untreated and IFN-γ treated melanoma cell lines using flow cytometry. Among the selected biomarkers, the IFN-γ-induced expression of PD-L1 and IDO1 was associated with an increased risk of relapse (P = .0001 and P = .013, respectively) and was also associated with death for IDO1 (P = .0005). In the future, this immunologic signature could permit the identification of patients at higher risk of relapse and justifying an adjuvant treatment using immunotherapy.

Keywords: flow cytometry; melanoma cell line; metastatic melanoma; prognostic markers; survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens, Neoplasm / metabolism*
  • B7-H1 Antigen
  • Biomarkers, Tumor / metabolism
  • Cell Line, Tumor
  • Disease-Free Survival
  • Female
  • Histocompatibility Antigens Class I / metabolism
  • Histocompatibility Antigens Class II / metabolism
  • Humans
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / metabolism*
  • Interferon-gamma / pharmacology
  • Lymphatic Metastasis
  • Male
  • Melanoma / metabolism*
  • Melanoma / secondary
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Monophenol Monooxygenase / metabolism*
  • Primary Cell Culture
  • Risk Assessment
  • Survival Rate
  • gp100 Melanoma Antigen / metabolism

Substances

  • Antigens, Neoplasm
  • B7-H1 Antigen
  • Biomarkers, Tumor
  • CD274 protein, human
  • CTAG1B protein, human
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • IDO1 protein, human
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Membrane Proteins
  • gp100 Melanoma Antigen
  • Interferon-gamma
  • Monophenol Monooxygenase