细胞生长
细胞周期
细胞
活力测定
生物
细胞凋亡
癌细胞
A549电池
作者
Ji-Ae Shin,Dong-Hoon Won,Neeti Swarup,Min-Hye Ahn,Seung-Ok Yang,Kunal Chawla,Ji Hoon Kim,Su-Jung Choi,Chi-Hyun Ahn,Kyu-Young Oh,Hye-Jung Yoon,Jae-Il Lee,Seong-Doo Hong,Kyoung-Ok Hong,Sung-Dae Cho
出处
期刊:Phytomedicine
[Elsevier BV]
日期:2021-10-01
卷期号:91: 153670-
被引量:1
标识
DOI:10.1016/j.phymed.2021.153670
摘要
Abstract Background Sedum species are reported to possess diverse pharmacological activities in various solid tumors. However, the anticancer functions of Sedum orizyfolium and its constituents have never been determined in human cancers. Purpose The present study focused on addressing the inhibition efficacy of the methanol extract of S. orizyfolium (MESO) and its constituents and the molecular mechanism underlying invasion and epithelial-to-mesenchymal transition (EMT) in oral squamous cell carcinoma (OSCC) cell lines. Study design/Methods After MESO treatment, a wound-healing assay, an invasion assay, and immunocytochemistry were performed in OSCC cell lines, coupled with in silico analysis and immunohistochemistry in OSCC patient samples, to investigate the role of the EMT transcription factor Slug. Trehalose, an active component of MESO, was identified through gas chromatography–mass spectrometry. Results Among the methanol extracts of 18 various wild plants from South Korea, MESO exhibited the highest anticancer functionality in OSCC cells by downregulating Slug expression. In silico analysis and immunohistochemistry indicated that elevated Slug levels are remarkably associated with tumor progression and invasion in patients with OSCC, suggesting that changes in Slug expression alter EMT progression and invasion in OSCC. Notably, treatment with trehalose, a sugar component of MESO, inhibited invasiveness and Slug expression in OSCC cells. Conclusion Cumulatively, this study highlighted the beneficial role of MESO and trehalose in the inhibition of invasiveness of OSCC cells via suppression of Slug expression and suggested a new design for potential chemotherapeutic drugs against OSCC.
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