| Literature DB >> 33110200 |
Ryo Saito1, Katsutoshi Shoda1, Suguru Maruyama1, Atsushi Yamamoto1, Koichi Takiguchi1, Shinji Furuya1, Naohiro Hosomura1, Hidenori Akaike1, Yoshihiko Kawaguchi1, Hidetake Amemiya1, Hiromichi Kawaida1, Makoto Sudo1, Shingo Inoue1, Hiroshi Kono1, Katsue Suzuki-Inoue2, Daisuke Ichikawa3.
Abstract
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.Entities:
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Year: 2020 PMID: 33110200 PMCID: PMC7851124 DOI: 10.1038/s41416-020-01134-7
Source DB: PubMed Journal: Br J Cancer ISSN: 0007-0920 Impact factor: 7.640