HS-1200 Induces Apoptosis and Inhibits Epithelial-Mesenchymal Transition in Oral Squamous Carcinoma

Young-jin Kim, I. Choi, Hae-Mi Kang, Odgerel Zunduijamts, In-Ryoung Kim, B. Park
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Abstract

Objectives: HS-1200 is a synthetic derivative of bile acid that has been proven to induce apoptosis in various types of cancer cells. However, whether HS-1200 inhibits metastasis in oral cancer has not yet been determined. Therefore, this study aims to evaluate the anti-cancer effect of HS-1200 through the inhibition of EMT in human oral squamous cell carcinoma (OSCC). Methods: The cytotoxicity effect of HS-1200 was assessed using an MTT assay. Furthermore, the cell migration and invasion ratios were obtained using a wound-healing assay and a transwell migration assay. The expressions of protein and mRNA levels were measured using a western blot analysis and real-time PCR. Results: HS-1200 was observed to inhibit the metastasis of cancer cells by regulating EMT in SCC-25 and HSC-3 cells. Conclusions: HS-1200 exhibits considerable potential as a treatment for OSCC.
HS-1200诱导口腔鳞癌细胞凋亡并抑制上皮-间质转化
目的:HS-1200是胆汁酸的合成衍生物,已被证明可诱导多种类型的癌细胞凋亡。然而,HS-1200是否能抑制口腔癌的转移尚未确定。因此,本研究旨在通过对EMT在人口腔鳞状细胞癌(OSCC)中的抑制作用来评价HS-1200的抗癌作用。方法:采用MTT法测定HS-1200的细胞毒作用。此外,通过伤口愈合实验和跨井迁移实验获得细胞迁移率和侵袭率。采用western blot和real-time PCR检测蛋白表达和mRNA表达水平。结果:HS-1200通过调节SCC-25和HSC-3细胞的EMT来抑制癌细胞转移。结论:HS-1200作为OSCC的治疗具有相当大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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