A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations

BMC Cancer. 2020 Nov 3;20(1):1058. doi: 10.1186/s12885-020-07567-w.

Abstract

Background: Cell lines are extremely useful for both basic and clinical research. Thus, establishing endometrial cancer cell lines with malignant histology is important. This study aimed to extensively characterize an endometrial clear cell carcinoma cell line.

Methods: This cell line, named 150,057, was derived from the endometrial clear cell cancer of a 63-year-old woman. The morphology, chromosomes, chemosensitivity, tumor markers, xenotransplantation characteristics, and cancer-related genes of the cell line were characterized.

Results: This cell line exhibited adequate growth, being passaged more than 70 times. The morphology of the cells was polygonal with a cobblestone-like appearance. Karyotyping of the cell line revealed a hypodiploid chromosomal number. 150057 cells expressed CA19-9 and CA125. The cell line was sensitive to doxorubicin, paclitaxel, carboplatin, and cisplatin. After the cells were transplanted into the subcutaneous region of non-obese diabetic-severe combined immunodeficiency mice, they generated xenograft tumors with similar histology as the original tumor. A total of 59 somatic nucleotide mutations were identified in 25 of the 53 examined tumor suppressor genes and oncogenes. Two novel mutations were found in FGFR3 and ARID1A.

Conclusion: We established and characterized an endometrial clear cell carcinoma cell line that may be useful in carcinogenesis and treatment research for endometrial cancer.

Keywords: Cell line; Clear cell carcinoma; Endometrium; Mutation; Proliferation.

MeSH terms

  • Adenocarcinoma, Clear Cell / genetics
  • Adenocarcinoma, Clear Cell / pathology*
  • Animals
  • Cell Line, Tumor
  • DNA-Binding Proteins / genetics*
  • Endometrial Neoplasms / genetics
  • Endometrial Neoplasms / pathology*
  • Female
  • Humans
  • Karyotyping
  • Mice
  • Middle Aged
  • Mutation*
  • Neoplasm Transplantation
  • Receptor, Fibroblast Growth Factor, Type 3 / genetics*
  • Serial Passage
  • Transcription Factors / genetics*

Substances

  • ARID1A protein, human
  • DNA-Binding Proteins
  • Transcription Factors
  • FGFR3 protein, human
  • Receptor, Fibroblast Growth Factor, Type 3