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Volume 195, Issue 1, Pages 85-91 (November 2009)


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Establishment and conventional cytogenetic characterization of three gastric cancer cell lines

Mariana Ferreira LealaCorresponding Author Informationemail address, José Luiz Martins do Nascimentob, Carla Elvira Araújo da Silvac, Maria Fernanda Vita Lamarãoc, Danielle Queiroz Calcagnoc, André Salim Khayata, Paulo Pimentel Assumpçãod, Isabel Rosa Cabralc, Marília de Arruda Cardoso Smitha, Rommel Rodríguez Burbanoc

Received 4 February 2009; received in revised form 3 April 2009; accepted 15 April 2009.

Abstract 

Gastric cancer is the fourth most frequent type of cancer and the second most frequent cause of cancer mortality worldwide. Only a modest number of gastric carcinoma cell lines have been isolated thus far. Here we describe the establishment and cytogenetic characterization of three new gastric cancer cell lines obtained from primary gastric adenocarcinoma (ACP02 and ACP03) and cancerous ascitic fluid (AGP01) of individuals from northern Brazil. ACP02, ACP03, and AGP01 cell lines are presently in the 60th passage. The cell lines grew in a disorganized single layer with some agglomerations and heterogeneous divisions (bipolar and multipolar). All cell lines exhibited a composite karyotype with several clonal chromosome alterations. Trisomy 8 was the most frequent alteration. Chromosome 8 aneusomy was confirmed by fluorescence in situ hybridization. All cell lines also exhibited trisomy 7 and deletion of chromosome arm 17p. These results suggest that, although frequent chromosome alterations are commonly observed due to culture process, the ACP02, ACP03, and AGP01 cell lines and primary gastric cancer from individuals of northern Brazil share genetic alterations, supporting use of these cell lines as a model of gastric carcinogenesis in this population.

a Genetics Division, Department of Morphology and Genetics, Federal University of São Paulo, Rua Botucatu 740, Ed. Leitão da Cunha, São Paulo, CEP 04023-900, São Paulo, SP, Brazil

b Laboratory of Cellular and Molecular Neurochemistry, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil

c Human Cytogenetics Laboratory, Institute of Biological Sciences, Federal University of Pará, Belém, PA, Brazil

d João de Barros Barreto University Hospital, Federal University of Pará, Belém, PA, Brazil

Corresponding Author InformationCorresponding author. Tel.: +55-11-55764260; fax: +55-11-55764264.

PII: S0165-4608(09)00239-8

doi:10.1016/j.cancergencyto.2009.04.020


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