Establishment and Characterization of a New Pancreatic Ductal Adenocarcinoma Cell Line Capan-26

Anticancer Res. 2021 Mar;41(3):1401-1406. doi: 10.21873/anticanres.14897.

Abstract

Background/aim: Pancreatic ductal adenocarcinoma is one of the deadliest forms of human cancer. Since only a vast panel of cell lines can fully recapitulate disease heterogeneity, our aim was to establish a new pancreatic cancer cell line.

Materials and methods: Newly established pancreatic ductal adenocarcinoma cell line Capan-26 was characterized by assessing growth rate, tumor and stem cell marker expression, colony forming efficiency, mutations of KRAS and TP53 genes, karyotype and sensitivity to drug treatment.

Results: Cell doubling time was 74 h. We detected CA19-9, CEACAM6, CD44, OCT4 and ZEB1 expression in Capan-26 cell line. Cells formed colonies in soft agar, have a deletion of KRAS exon 3 and a point mutation V172F in TP53 exon 5. They are a mixed aneuploid/polyploid population with high sensitivity to gemcitabine.

Conclusion: Capan-26 is a unique cell line that may be used to study the mechanism of pancreatic cancer.

Keywords: Pancreatic cancer; cell line establishment; chemotherapy.

MeSH terms

  • Aged
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Antimetabolites, Antineoplastic / pharmacology
  • Carcinoma, Pancreatic Ductal / genetics
  • Carcinoma, Pancreatic Ductal / metabolism
  • Carcinoma, Pancreatic Ductal / pathology*
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Proliferation / genetics
  • Deoxycytidine / analogs & derivatives
  • Deoxycytidine / pharmacology
  • Female
  • GPI-Linked Proteins / genetics
  • GPI-Linked Proteins / metabolism
  • Gemcitabine
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Karyotyping
  • Mutation
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / metabolism
  • Pancreatic Neoplasms / pathology*
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Tumor Suppressor Protein p53 / genetics

Substances

  • Antigens, CD
  • Antimetabolites, Antineoplastic
  • CEACAM6 protein, human
  • Cell Adhesion Molecules
  • GPI-Linked Proteins
  • KRAS protein, human
  • Octamer Transcription Factor-3
  • POU5F1 protein, human
  • Tumor Suppressor Protein p53
  • Deoxycytidine
  • Proto-Oncogene Proteins p21(ras)
  • Gemcitabine