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Hydrogen sulfide donor GYY4137 suppresses proliferation of human colorectal cancer Caco-2 cells by inducing both cell cycle arrest and cell death

Conflicting data regarding the ability of hydrogen sulfide (H(2)S), which reaches high levels in the large intestine owing to biosynthesis in the intestinal cells and intestinal bacteria, to promote or inhibit colorectal cancer cell proliferation have been reported recently. In the present study, th...

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Detalles Bibliográficos
Autores principales: Sakuma, Satoru, Minamino, Saaya, Takase, Maya, Ishiyama, Yoshitaka, Hosokura, Hiroyuki, Kohda, Tetsuya, Ikeda, Yukino, Fujimoto, Yohko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699460/
https://www.ncbi.nlm.nih.gov/pubmed/31440595
http://dx.doi.org/10.1016/j.heliyon.2019.e02244
Descripción
Sumario:Conflicting data regarding the ability of hydrogen sulfide (H(2)S), which reaches high levels in the large intestine owing to biosynthesis in the intestinal cells and intestinal bacteria, to promote or inhibit colorectal cancer cell proliferation have been reported recently. In the present study, the effect of H(2)S on the proliferation of the human colorectal cancer cell line Caco-2 was examined by using the H(2)S donor GYY4137. At concentrations of 0.5 mM and 1.0 mM, GYY4137 significantly inhibited Caco-2 cell viability. Cell cycle analysis, and apoptosis and necrosis detection revealed that the anti-proliferative effect of GYY4137 was partially attributable to the induction of S-G(2)/M cell cycle arrest, apoptosis and necrosis. These results suggest that H(2)S has the potential to suppress human colorectal cancer cell proliferation by influencing both cell cycle and cell death.