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通过对MMP12进行上调,HOXB9促进了喉状细胞癌的进展
Chuanhui Sun1, Hua Deng1, Qiuying Li2
1Department of Otorhinolaryngology, The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine, 550001, Guiyang, Guizhou, People's Republic of China.
Functional & integrative genomics
|April 17, 2024
概括
通过增加MMP12活性,HOXB9驱动喉状细胞癌 (LSCC) 的进展. 使用CRISPR/Cas9破坏HOXB9,可以抑制LSCC细胞的生长,迁移和入侵,从而提供治疗见解.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
背景情况:
- 包括HOXB9在内的HOX基因家族与各种癌症有关.
- 了解HOXB9在喉状细胞癌 (LSCC) 中的作用对于预后和治疗至关重要.
研究的目的:
- 研究HOXB9在LSCC细胞增殖和侵入中的调控机制.
- 确定HOXB9在LSCC发展中的下游目标和途径.
主要方法:
- 在LSCC细胞系中进行CRISPR/Cas9基因编辑.
- 对细胞活力 (CCK-8),增殖 (流细胞计),亡 (道) 和迁移/入侵 (Transwell) 的检测.
- 在裸体小鼠中进行体内瘤生长研究;微阵列,西部斑点,IHC,ChIP和光酶试验用于基因验证.
主要成果:
- 通过CRISPR/Cas9敲除HOXB9显著抑制了LSCC细胞的增殖,迁移和入侵,同时促进了细胞亡.
- 发现HOXB9直接上调MMP12的转录活性.
- 霍克斯B9通过其下游目标基因MMP12促进LSCC的进展.
结论:
- HOXB9是LSCC进展的一个关键驱动因素.
- 针对HOXB9,可能通过其与MMP12的相互作用,可能是LSCC的治疗策略.
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