ERK/MAPK信号通路 在清细胞癌中通过ETS1调节MMP2
Hai-Bin Chen1,2, Wei Li1, Zhan Yang1
1Department of Urology, the Second Hospital of Hebei Medical University, Shijiazhuang, 050061, China.
Current molecular medicine
|May 31, 2023
概括
高ETS1表达与清细胞细胞癌 (ccRCC) 的进展相关. 向ETS1和ERK可能会抑制ccRCC细胞的增殖,迁移和入侵,这表明ETS1是治疗点.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 在清细胞细胞癌 (ccRCC) 组织中,ETS1表达升高.
- 关于ETS1在ccRCC发病过程中的确切作用尚不清楚.
研究的目的:
- 研究ETS1表达和ccRCC进展之间的关联.
- 阐明ETS1在ccRCC细胞增殖,迁移和入侵中的功能作用.
主要方法:
- 使用STRING进行蛋白质与蛋白质相互作用网络分析.
- 细胞活力,增殖,迁移和入侵测定 (CCK-8,克隆原生,伤口愈合,Transwell).
- 对蛋白质表达的西部斑分析;使用PERK和ERK通路抑制剂.
主要成果:
- 在ccRCC组织中显著增加ETS1表达及其与晚期瘤阶段,淋巴结转移和更高等级的相关性 (p<0.05).
- 抑制ETS1和PERK抑制抑制了ccRCC细胞的增殖,迁移和入侵.
- ETS1 knockdown 降低了MMP-2的表达;ERK抑制影响了ETS1和MMP-2的表达.
结论:
- 提高ETS1表达与ccRCC进展有关.
- ETS1通过MMP2的升级调节来促进ccRCC的扩散.
- 结合ETS1敲除和ERK抑制显示了ccRCC的治疗潜力.
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