The Second Clinical Medical College, Zhejiang Chinese Medicine University, Hangzhou 310053, Zhejiang Province, China.
Cancer Institute of Integrated Tradition Chinese and Western Medicine, Zhejiang Academy of Traditional Chinese Medicine, Tongde Hospital of Zhejiang Province, Hangzhou 310012, Zhejiang Province, China.
Biomed Res Int. 2022 Aug 25;2022:7029182. doi: 10.1155/2022/7029182. eCollection 2022.
This study is aimed at exploring whether Xiaotan Sanjie decoction (XTSJ) inhibits gastric cancer (GC) proliferation and metastasis by regulating lncRNA-ATB expression. qRT-PCR and Western blot were used to analyze lncRNA-ATB and downstream-regulated genes/proteins in human GC cells. CCK8, Edu, and flow cytometry assays were used to detect the inhibitory effect of XTSJ on cell proliferation and apoptosis. Moreover, transwell and wound healing assays were used to detect the inhibitory effect of XTSJ on migration and invasion. qRT-PCR and Western blot were used to detect regulated genes and proteins levels. The HGC-27 cell line was used for follow-up analysis due to the high level of lncRNA-ATB and cell characteristics. XTSJ inhibited the proliferation and metastasis of HGC-27 in a dose-dependent manner. Further research found that XTSJ downregulated lncRNA-ATB, Vimentin, and N-cadherin, while it upregulated miR-200a and E-cadherin in a dose-dependent manner. XTSJ also upregulated Caspase 3, Caspase 9, Bax, and downregulated Bcl-2. Furthermore, XTSJ inhibited tumor growth and downregulated EMT signaling pathways. These results indicate that XTSJ may affect EMT and Bcl-2 signaling pathways by regulating lncRNA-ATB and miR-200a, thus inhibiting proliferation, migration, and invasion of HGC-27 cells. Therefore, XTSJ may be an effective treatment for the high levels of lncRNA-ATB in GC.
本研究旨在探讨消痰散结汤(XTSJ)是否通过调节 lncRNA-ATB 的表达来抑制胃癌(GC)的增殖和转移。采用 qRT-PCR 和 Western blot 分析人 GC 细胞中 lncRNA-ATB 和下游调控基因/蛋白。CCK8、Edu 和流式细胞术检测 XTSJ 对细胞增殖和凋亡的抑制作用。此外,Transwell 和划痕愈合实验检测 XTSJ 对迁移和侵袭的抑制作用。qRT-PCR 和 Western blot 检测调节基因和蛋白水平。由于 lncRNA-ATB 水平高和细胞特征,选择 HGC-27 细胞系进行后续分析。XTSJ 呈剂量依赖性抑制 HGC-27 的增殖和转移。进一步研究发现,XTSJ 下调 lncRNA-ATB、Vimentin 和 N-cadherin,同时呈剂量依赖性上调 miR-200a 和 E-cadherin。XTSJ 还上调 Caspase 3、Caspase 9、Bax,下调 Bcl-2。此外,XTSJ 抑制肿瘤生长并下调 EMT 信号通路。这些结果表明,XTSJ 可能通过调节 lncRNA-ATB 和 miR-200a 影响 EMT 和 Bcl-2 信号通路,从而抑制 HGC-27 细胞的增殖、迁移和侵袭。因此,XTSJ 可能是治疗 GC 中 lncRNA-ATB 水平升高的有效方法。