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Platelets enhance malignant behaviours of gastric cancer cells via direct contacts

In this study, we aimed to analyse human cancer cell–platelet interactions in functional cell analyses and explore the molecular mechanisms behind tumour progression. Various functional analyses of gastric cancer (GC) cells were performed after direct/indirect co-incubation with platelets derived fr...

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Detalles Bibliográficos
Autores principales: Saito, Ryo, Shoda, Katsutoshi, Maruyama, Suguru, Yamamoto, Atsushi, Takiguchi, Koichi, Furuya, Shinji, Hosomura, Naohiro, Akaike, Hidenori, Kawaguchi, Yoshihiko, Amemiya, Hidetake, Kawaida, Hiromichi, Sudo, Makoto, Inoue, Shingo, Kono, Hiroshi, Suzuki-Inoue, Katsue, Ichikawa, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851124/
https://www.ncbi.nlm.nih.gov/pubmed/33110200
http://dx.doi.org/10.1038/s41416-020-01134-7
Descripción
Sumario:In this study, we aimed to analyse human cancer cell–platelet interactions in functional cell analyses and explore the molecular mechanisms behind tumour progression. Various functional analyses of gastric cancer (GC) cells were performed after direct/indirect co-incubation with platelets derived from GC patients. Further detailed expression and signalling analyses were performed after co-culture with direct and indirect GC cells–platelet contact. Malignant behaviours of cancer cells, such as proliferation, migration, invasion and adhesion, were significantly enhanced after direct co-incubation with platelets. Microarray analyses demonstrated changes in multiple genes, including epithelial–mesenchymal transition (EMT)-related genes. Among them, matrix metalloproteinase 9 was notably upregulated, which was validated by quantitative reverse transcription–polymerase chain reaction and western blot. Further, this change was only observed after direct co-incubation with platelets. This study demonstrated that platelets from GC patients promote malignant behaviours of GC cells through EMT-related signalling, especially by direct contact with tumour cells.