Cellular origin and clonal evolution of human dedifferentiated liposarcoma

Nat Commun. 2024 Sep 12;15(1):7941. doi: 10.1038/s41467-024-52067-1.

Abstract

Dedifferentiated liposarcoma (DDLPS) is the most frequent high-grade soft tissue sarcoma subtype. It is characterized by a component of undifferentiated tumor cells coexisting with a component of well-differentiated adipocytic tumor cells. Both dedifferentiated (DD) and well-differentiated (WD) components exhibit MDM2 amplification, however their cellular origin remains elusive. Using single-cell RNA sequencing, DNA sequencing, in situ multiplex immunofluorescence and functional assays in paired WD and DD components from primary DDLPS tumors, we characterize the cellular heterogeneity of DDLPS tumor and micro-environment. We identify a population of tumor adipocyte stem cells (ASC) showing striking similarities with adipocyte stromal progenitors found in white adipose tissue. We show that tumor ASC harbor the ancestral genomic alterations of WD and DD components, suggesting that both derive from these progenitors following clonal evolution. Last, we show that DD tumor cells keep important biological properties of ASC including pluripotency and that their adipogenic properties are inhibited by a TGF-β-high immunosuppressive tumor micro-environment.

MeSH terms

  • Adipocytes* / metabolism
  • Adipocytes* / pathology
  • Aged
  • Cell Dedifferentiation / genetics
  • Cell Differentiation / genetics
  • Clonal Evolution*
  • Female
  • Humans
  • Liposarcoma* / genetics
  • Liposarcoma* / metabolism
  • Liposarcoma* / pathology
  • Male
  • Middle Aged
  • Neoplastic Stem Cells / metabolism
  • Neoplastic Stem Cells / pathology
  • Proto-Oncogene Proteins c-mdm2* / genetics
  • Proto-Oncogene Proteins c-mdm2* / metabolism
  • Single-Cell Analysis
  • Transforming Growth Factor beta / metabolism
  • Tumor Microenvironment* / genetics

Substances

  • Proto-Oncogene Proteins c-mdm2
  • MDM2 protein, human
  • Transforming Growth Factor beta