Establishment and characterization of NCC-DFSP3-C1: a novel patient-derived dermatofibrosarcoma protuberans cell line

Hum Cell. 2020 Jul;33(3):894-903. doi: 10.1007/s13577-020-00365-3. Epub 2020 Apr 30.

Abstract

Dermatofibrosarcoma protuberans (DFSP) is the most common dermal sarcoma; it is characterized by the presence of the COL1A1-PDGFB translocation, which causes the constitutive activation of the platelet-derived growth factor β (PDGFB) signaling pathway. DFSP frequently exhibits local recurrence and is refractory to conventional chemotherapy. Therefore, a novel therapeutic strategy is required for improving the prognosis of DFSP. Although patient-derived cell lines are important tools for pre-clinical studies, currently, only a few such cell lines are available for DFSP in cell banks. Here, we report the establishment of a novel DFSP cell line. Using a surgically resected metastatic tumor tissue from a patient with DFSP, we established a cell line called NCC-DFSP3-C1. The NCC-DFSP3-C1 cells had a COL1A1-PDGFB translocation and retained the same copy number aberrations as the original tumor tissue. NCC-DFSP3-C1 cells exhibited constant growth, spheroid formation, and invasive ability. By screening a drug library, we identified anti-cancer agents with inhibitory effects on the proliferation of NCC-DFSP3-C1 cells; these anti-cancer agents included proteasomal, histone deacetylase, and kinase inhibitors. We concluded that the NCC-DFSP3-C1 cell line may serve as a useful tool for performing basic and pre-clinical studies on DFSP.

Keywords: Dermatofibrosarcoma protuberans; Fusion gene; Patient-derived cancer model; Patient-derived cell line; Sarcoma.

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Collagen Type I / genetics
  • Collagen Type I, alpha 1 Chain
  • Dermatofibrosarcoma / genetics*
  • Dermatofibrosarcoma / pathology*
  • Histone Deacetylases / pharmacology
  • Humans
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-sis / genetics
  • Proto-Oncogene Proteins c-sis / metabolism
  • Signal Transduction / genetics
  • Signal Transduction / physiology
  • Translocation, Genetic

Substances

  • Antineoplastic Agents
  • Collagen Type I
  • Collagen Type I, alpha 1 Chain
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-sis
  • Histone Deacetylases