Establishment and characterization of NCC-DDLPS3-C1: a novel patient-derived cell line of dedifferentiated liposarcoma.
Ryuto TsuchiyaYuki YoshimatsuRei NoguchiTakuya OnoAkane SeiFumitaka TakeshitaJun SugayaSuguru FukushimaAkihiko YoshidaSeiji OhtoriAkira KawaiTadashi KondoPublished in: Human cell (2021)
Dedifferentiated liposarcoma (DDLPS) is a highly malignant subtype of liposarcoma, with characteristic amplification of MDM2 and CDK4 (12q14-15). It is caused by the dedifferentiation of well-differentiated liposarcoma. DDLPS is refractory to conventional chemotherapy; thus, surgical resection is the primary treatment modality. However, complete resection of DDLPS is difficult because of its deep location, which results in poor prognosis. Therefore, novel systemic chemotherapy is required to improve the clinical outcome. Patient-derived cell lines are important tools in the development of novel chemotherapy. However, there are no DDLPS cell lines available from public cell banks. In this study, we established a novel DDLPS cell line, NCC-DDLPS3-C1, using a surgically resected specimen from a patient with DDLPS. NCC-DDLPS3-C1 cells retained the characteristic gene amplification of MDM2 and CDK4. In addition, other gene amplifications and losses related to the poor prognosis of DDLPS were also observed in concordance with the original tumor. The cells also exhibited rapid cell proliferation, aggressive invasion ability, spheroid formation ability, and tumorigenic ability in nude mice. Furthermore, a drug-screening test showed significant antiproliferative effects of proteasome inhibitors and HDAC inhibitors. Thus, the NCC-DDLPS3-C1 cell line should be a useful tool for the development of novel chemotherapy for DDLPS.
Keyphrases
- poor prognosis
- long non coding rna
- induced apoptosis
- locally advanced
- cell proliferation
- cell cycle
- cell cycle arrest
- genome wide
- copy number
- squamous cell carcinoma
- nucleic acid
- endoplasmic reticulum stress
- type diabetes
- chemotherapy induced
- mental health
- stem cells
- lymph node
- cell death
- oxidative stress
- emergency department
- signaling pathway
- radiation therapy
- dna methylation
- case report
- drug induced
- combination therapy
- wild type
- bone marrow
- genome wide analysis
- loop mediated isothermal amplification