Targeting sarcoma tumor-initiating cells through differentiation therapy

Stem Cell Res. 2017 May:21:117-123. doi: 10.1016/j.scr.2017.04.004. Epub 2017 Apr 13.

Abstract

Human leukocyte antigen class I (HLA-I) down-regulation has been reported in many human cancers to be associated with poor clinical outcome. However, its connection to tumor-initiating cells (TICs) remains unknown. In this study, we report that HLA-I is down-regulated in a subpopulation of cells that have high tumor initiating capacity in different types of human sarcomas. Detailed characterization revealed their distinct molecular profiles regarding proliferation, apoptosis and stemness programs. Notably, these TICs can be induced to differentiate along distinct mesenchymal lineages, including the osteogenic pathway. The retinoic acid receptor signaling pathway is overexpressed in HLA-1 negative TICs. All-trans retinoic acid treatment successfully induced osteogenic differentiation of this subpopulation, in vitro and in vivo, resulting in significantly decreased tumor formation. Thus, our findings indicate down-regulated HLA-I is a shared feature of TICs in a variety of human sarcomas, and differentiation therapy strategies may specifically target undifferentiated TICs and inhibit tumor formation.

Keywords: Human leukocyte antigen class I; Sarcomas; Tumor-initiating cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Carcinogenesis / drug effects
  • Carcinogenesis / genetics
  • Carcinogenesis / pathology
  • Cell Differentiation* / drug effects
  • Cell Line, Tumor
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic / drug effects
  • HLA Antigens / immunology
  • Humans
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / pathology*
  • Osteogenesis / drug effects
  • Osteogenesis / genetics
  • Phenotype
  • Sarcoma / genetics
  • Sarcoma / pathology*
  • Sarcoma / therapy*
  • Tretinoin / pharmacology

Substances

  • HLA Antigens
  • Tretinoin