Establishment and characterization of a novel 'double-hit' follicular lymphoma cell line, FL-SJC

J Cell Mol Med. 2020 Jul;24(14):7928-7938. doi: 10.1111/jcmm.15425. Epub 2020 May 27.

Abstract

About 5 per cent of follicular lymphoma (FL) cases are double-hit (DH) lymphomas. Double-hit follicular lymphoma (DHFL) cell lines can improve our understanding and drug development on FL. But there are only few DHFL cell lines. Here, we established a new MYC/BCL2 DHFL cell line, FL-SJC. The cells were obtained from the hydrothorax of a patient with MYC/BCL2 DHFL and cultured for 140 passages in vitro. FL-SJC cells demonstrated CD19++ , CD20+ , CD22++ , HLA-DR+ , CD10+ , CD38+ , Lambda+ CD23- , CD5- and Kappa- . The chromosome karyotypic analysis confirmed the co-existence of t(8;22)(q24;q11) and t(14;18)(q32;q21), as well as additional abnormalities involving chromosomes 2 and 3. Fluorescence in situ hybridization analysis (FISH) showed IGH/BCL2 fusion gene and the MYC rearrangement. In addition, the FL-SJC cells displayed KMT2D/MLL2 and CREBBP gene mutations. After subcutaneous inoculation of FL-SJC cells, the SCID mice developed solid tumour masses within 6-8 weeks. FL-SJC cells were proven to be free of Epstein-Barr (EB) virus infection and be multidrug-resistant. In a conclusion, the FL-SJC cell line has been identified as a novel MYC/BCL2 double-hit follicular lymphoma that can be used as a potentially available tool for the clinical and basic research, together with the drug development for MYC/BCL2 DHFL.

Keywords: BCL2; Double-hit lymphoma; FL-SJC cell line; Follicular lymphoma; MYC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers, Tumor*
  • Biopsy
  • Cell Line, Tumor*
  • Chromosome Deletion
  • Disease Models, Animal
  • Drug Resistance, Neoplasm
  • Heterografts
  • Humans
  • Immunohistochemistry
  • Immunophenotyping
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Lymphoma, Follicular / diagnosis
  • Lymphoma, Follicular / genetics*
  • Lymphoma, Follicular / therapy
  • Male
  • Mice
  • Middle Aged
  • Mutation*
  • Positron Emission Tomography Computed Tomography
  • Translocation, Genetic

Substances

  • Biomarkers, Tumor