Conventional cytogenetic characterization of a new cell line, ACP01, established from a primary human gastric tumor

• Autor(a) principal: Lima, Eleonidas Moura
• Data de Publicação: 2004
• Outros Autores: Rissino, Jorge Dores, Harada, Maria Lucia, Assumpção, Paulo Pimentel [UNIFESP], Demachki, Samia, Guimarães, Adriana Costa, Casartelli, Carla [UNIFESP], Smith, Marilia de Arruda Cardoso [UNIFESP], Burbano, Rommel Rodríguez [UNIFESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNIFESP
• Texto Completo: http://dx.doi.org/10.1590/S0100-879X2004001200008; http://repositorio.unifesp.br/handle/11600/2318
• topic: Cell line ACP01; Human gastric adenocarcinoma; In vitro immortalization; Chromosome 8 trisomy; Clonal expansion

Gastric cancer is the second most frequent type of neoplasia and also the second most important cause of death in the world. Virtually all the established cell lines of gastric neoplasia were developed in Asian countries, and western countries have contributed very little to this area. In the present study we describe the establishment of the cell line ACP01 and characterize it cytogenetically by means of in vitro immortalization. Cells were transformed from an intestinal-type gastric adenocarcinoma (T4N2M0) originating from a 48-year-old male patient. This is the first gastric adenocarcinoma cell line established in Brazil. The most powerful application of the cell line ACP01 is in the assessment of cytotoxicity. Solid tumor cell lines from different origins have been treated with several conventional and investigational anticancer drugs. The ACP01 cell line is triploid, grows as a single, non-organized layer, similar to fibroblasts, with focus formation, heterogeneous division, and a cell cycle of approximately 40 h. Chromosome 8 trisomy, present in 60% of the cells, was the most frequent cytogenetic alteration. These data lead us to propose a multifactorial triggering of gastric cancer which evolves over multiple stages involving progressive genetic changes and clonal expansion.