FOXD3 Regulates VISTA Expression in Melanoma

  • Sheera Rosenbaum
  • , Meghan Knecht
  • , Mehri Mollaee
  • , Zhijiu Zhong
  • , Dan A. Erkes
  • , Peter A. McCue
  • , Inna Chervoneva
  • , Adam Berger
  • , Jennifer A. Lo
  • , David E. Fisher
  • , Jeffrey E. Gershenwald
  • , Michael A. Davies
  • , Timothy J. Purwin
  • , Andrew E. Aplin

Research output: Contribution to journalArticlepeer-review

67 Scopus citations

Abstract

Immune checkpoint inhibitors have improved patient survival in melanoma, but the innate resistance of many patients necessitates the investigation of alternative immune targets. Many immune checkpoint proteins lack proper characterization, including V-domain Ig suppressor of T cell activation (VISTA). VISTA expression on immune cells can suppress T cell activity; however, few studies have investigated its expression and regulation in cancer cells. In this study, we observe that VISTA is expressed in melanoma patient samples and cell lines. Tumor cell-specific expression of VISTA promotes tumor onset in vivo, associated with increased intratumoral T regulatory cells, and enhanced PDL-1 expression on tumor-infiltrating macrophages. VISTA transcript levels are regulated by the stemness factor Forkhead box D3 (FOXD3). BRAF inhibition upregulates FOXD3 and reduces VISTA expression. Overall, this study demonstrates melanoma cell expression of VISTA and its regulation by FOXD3, contributing to the rationale for therapeutic strategies that combine targeted inhibitors with immune checkpoint blockade.

Original languageEnglish
Pages (from-to)510-524.e6
JournalCell Reports
Volume30
Issue number2
DOIs
StatePublished - Jan 14 2020
Externally publishedYes

Keywords

  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • B7 Antigens/biosynthesis
  • Cell Line, Tumor
  • Female
  • Forkhead Transcription Factors/genetics
  • Humans
  • Lymphocytes, Tumor-Infiltrating/immunology
  • Male
  • Melanoma, Experimental/genetics
  • Melanoma/genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Middle Aged
  • Proto-Oncogene Proteins B-raf/antagonists & inhibitors
  • RNA, Messenger/genetics
  • Survival Analysis
  • T-Lymphocytes/immunology

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