6533b853fe1ef96bd12ad703

RESEARCH PRODUCT

New cell lines of gastric and pancreatic cancer: distinct morphology, growth characteristics, expression of epithelial and immunoregulatory antigens.

K H Meyer Zum BüschenfeldeMichael HeikeAlexander KnuthO RöhrigRoland MollHelmut E. GabbertWolfgang Dippold

subject

Pathologymedicine.medical_specialtyCell divisionCellular differentiationCellBiologyAdenocarcinomaEpitheliumPathology and Forensic MedicineCytokeratinNude mouseStomach NeoplasmsPancreatic cancermedicineBiomarkers TumorHumansNeoplasm MetastasisMolecular BiologyCell Line TransformedLiver NeoplasmsCell DifferentiationCell BiologyGeneral Medicinebiology.organism_classificationmedicine.diseasePancreatic NeoplasmsMicroscopy Electronmedicine.anatomical_structureCell cultureAntigens SurfaceCancer researchMicroscopy Electron ScanningPancreasCell Division

description

Two new cell lines from stomach cancers and one from a pancreatic carcinoma are presented. MZ-GC-1 was established from a hepatic metastasis of a well differentiated gastric adenocarcinoma. MZ-GC-2 was derived from ascites induced by a poorly differentiated gastric adenocarcinoma. MZ-PC-1 originated from the pleural effusion of a moderately well differentiated pancreatic ductal adenocarcinoma. MZ-GC-1 cells were adherent and partially polarized, connected tightly via desmosomes. In contrast MZ-GC-2 cells consisted of slightly adherent or floating subpopulations and displayed no desmosomes. MZ-PC-1 cells were adherent and showed polarized growth, connected by apical junctional complexes. Cell doubling times were 7 days for MZ-GC-1 and 45 h for MZ-GC-2 and MZ-PC-1 cells. MZ-GC-2 and MZ-PC-1 gave rise to nude mouse tumours, resembling the original lesions. Chromosome analysis of the cell lines revealed a high range of numerical abnormalities. Each cell line had cytokeratin patterns fitting well to typical in vivo patterns. Furthermore the cell lines expressed a panel of antigens typical for gastrointestinal epithelia. Unique for MZ-PC-1 were high amounts of secreted Ca19-9. gamma-Interferon enhanced HLA-class I antigens up to twofold and induced ICAM-1 expression on each cell line. HLA-class II antigens were differentially enhanced by gamma-interferon. Due to their distinct characteristics the three tumour cell lines may be useful models in the investigation of the cell biology and immunogenicity of gastrointestinal tumours.

10.1007/bf00191347https://pubmed.ncbi.nlm.nih.gov/7599790