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Cytotoxic effects of human calprotectin on gastric cancer cell line is attenuated by etoposide

AIM: In this paper effect of combinational usage of calprotectin and etoposide on AGS cell line is studied. BACKGROUND: Application of combined toxic agents such as etoposide and cicplatin are commonly used for chemotherapy purposes. As a matter of fact, calprotectin and etoposide were both applied...

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Detalles Bibliográficos
Autores principales: Zali, Hakimeh, Zamanian-Azodi, Mona, Shokrgozar, Mohamad Ali, Rezaei-Tavirani, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Institute for Gastroenterology and Liver Diseases 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017472/
https://www.ncbi.nlm.nih.gov/pubmed/24834214
Descripción
Sumario:AIM: In this paper effect of combinational usage of calprotectin and etoposide on AGS cell line is studied. BACKGROUND: Application of combined toxic agents such as etoposide and cicplatin are commonly used for chemotherapy purposes. As a matter of fact, calprotectin and etoposide were both applied on human gastric adenocarcinoma cell line (AGS) as antitumor agents. Both calprotectin and etoposide are topo II inhibitor. Etoposide is a lipophilic agent that can easily transport from membrane while calprotectin active intracellular pathway, probably by membrane surface receptor. PATIENTS AND METHODS: Calprotectin was purified from human neutrophil by chromatography methods. The human gastric adenocarcinoma cell line was exposed to different concentrations and combinations of calprotectin and etoposide. MTT assay was applied for evaluation of cytotoxicity assay. RESULTS: Viability of AGS cell line was reduced in high dosages of calprotectin and etposide. In fact, overnight incubation of these two agents together has been shown less effective than individual usage. CONCLUSION: The result indicates that, the combination of both calprotectin and etoposide is considerably less cytotoxic on gastric cancer cells (AGS) than applying individually.