[HTML][HTML] Overexpression of CBS/H2S inhibits proliferation and metastasis of colon cancer cells through downregulation of CD44
Y Zhang, S Chen, J Zhu, S Guo, T Yue, H Xu… - Cancer Cell …, 2022 - Springer
Y Zhang, S Chen, J Zhu, S Guo, T Yue, H Xu, J Hu, Z Huang, Z Chen, P Wang, Y Liu
Cancer Cell International, 2022•SpringerBackground The role of hydrogen sulfide (H2S) in cancer biology is controversial, including
colorectal cancer. The bell-shaped effect of H2S refers to pro-cancer action at lower doses
and anti-cancer effect at higher concentrations. We hypothesized that overexpression of
cystathionine-beta-synthase (CBS)/H2S exerts an inhibitory effect on colon cancer cell
proliferation and metastasis. Methods Cell proliferation was assessed by Cell Counting Kit-8
(CCK-8), clone-formation and sphere formation assay. Cell migration was evaluated by …
colorectal cancer. The bell-shaped effect of H2S refers to pro-cancer action at lower doses
and anti-cancer effect at higher concentrations. We hypothesized that overexpression of
cystathionine-beta-synthase (CBS)/H2S exerts an inhibitory effect on colon cancer cell
proliferation and metastasis. Methods Cell proliferation was assessed by Cell Counting Kit-8
(CCK-8), clone-formation and sphere formation assay. Cell migration was evaluated by …
Background
The role of hydrogen sulfide (H2S) in cancer biology is controversial, including colorectal cancer. The bell-shaped effect of H2S refers to pro-cancer action at lower doses and anti-cancer effect at higher concentrations. We hypothesized that overexpression of cystathionine-beta-synthase (CBS)/H2S exerts an inhibitory effect on colon cancer cell proliferation and metastasis.
Methods
Cell proliferation was assessed by Cell Counting Kit-8 (CCK-8), clone-formation and sphere formation assay. Cell migration was evaluated by transwell migration assay. Intracellular H2S was detected by H2S probe. Chromatin immunoprecipitation (ChIP) analysis was carried out to examine DNA–protein interaction. Cell experiments also included western blotting, flow cytometry, immunohistochemistry (IHC) and immunofluorescence analysis. We further conducted in vivo experiments to confirm our conclusions.
Results
Overexpression of CBS and exogenous H2S inhibited colon cancer cell proliferation and migration in vitro. In addition, overexpression of CBS attenuated tumor growth and liver metastasis in vivo. Furthermore, CD44 and the transcription factor SP-1 was probably involved in the inhibitory effect of CBS/H2S axis on colon cancer cells.
Conclusions
Overexpression of CBS and exogenous provision of H2S inhibited colon cancer cell proliferation and migration both in vivo and in vitro. Molecular mechanisms might involve the participation of CD44 and the transcription factor SP-1.
Springer