Characterization and properties of nine human ovarian adenocarcinoma cell lines

SP Langdon, SS Lawrie, FG Hay, MM Hawkes… - Cancer research, 1988 - AACR
SP Langdon, SS Lawrie, FG Hay, MM Hawkes, A McDonald, IP Hayward, DJ Schol…
Cancer research, 1988AACR
Four series of cell lines have been derived from patients with ovarian adenocarcinoma. Nine
cell lines have been established at different stages of treatment: eight from malignant
effusions and one from a solid metastasis. Six lines were derived from the ascites or pleural
effusion of patients with poorly differentiated adenocarcinoma: PEO1, PEO4, and PEO6 from
one patient, PEA1 and PEA2 from a second, and PEO16 from a third. Three lines (PEO14
and PEO23 from ascites and TO14 from a solid metastasis) were derived from a patient with …
Abstract
Four series of cell lines have been derived from patients with ovarian adenocarcinoma. Nine cell lines have been established at different stages of treatment: eight from malignant effusions and one from a solid metastasis. Six lines were derived from the ascites or pleural effusion of patients with poorly differentiated adenocarcinoma: PEO1, PEO4, and PEO6 from one patient, PEA1 and PEA2 from a second, and PEO16 from a third. Three lines (PEO14 and PEO23 from ascites and TO14 from a solid metastasis) were derived from a patient with a well-differentiated serous adenocarcinoma. Each set of cell lines was morphologically distinct. The five cell lines PEO1, PEO4, PEO6, PEA1, and PEA2 had cloning efficiencies on plastic of 1–2% and only a few cells in these lines expressed alkaline phosphatase or vimentin. Only a low percentage of these cells reacted with the monoclonal antibodies 123C3 and 123A8 but most reacted with OC125. Conversely the cell lines PEO14, TO14, PEO23, and PEO16 were characterized by low cloning efficiency values (<0.05%), marked expression of alkaline phosphatase and vimentin, and good reaction with 123C3 and 123A8 but not OC125. These four cell lines also exhibited dome formation. Four of the cell lines, PEO1, PEO4, PEO6, and PEO16, have been xenografted into immune-deprived mice and found to be tumorigenic.
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