向MYH9抑制USP14介导的NAP1L1二维基化和细胞增殖在质瘤中
Zigui Chen1,2, Xin Yan3, Changfeng Miao4
1Cancer Center, Integrated Hospital of Traditional Chinese Medicine, Southern Medical University, 13 Shiliugang ST, Guangzhou, 510315, China.
Cancer cell international
|September 28, 2023
概括
氨酸重链9 (MYH9) 通过稳定NAP1L1.1.通过稳定NAP1L1.1.通过促进质瘤细胞增殖和特莫索洛米德耐药性. 向MYH9可能为质瘤患者提供新的治疗策略.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 氨酸重链9 (MYH9) 与各种疾病有关,但其在质瘤中的作用仍然基本不明.
- 了解MYH9的功能对于开发向性结质瘤治疗至关重要.
研究的目的:
- 调查MYH9在质瘤进展中的作用.
- 为了确定MYH9是否影响质瘤细胞中temozolomide化学阻力.
主要方法:
- 研究了MYH9对质瘤细胞增殖和temozolomide耐药性的影响.
- 进行了涉及MYH9,NAP1L1,USP14,c-Myc,CCND1和CDK4.4的机制研究.
- 分析了MYH9表达和患者存活率之间的相关性.
主要成果:
- MYH9显著增加了质瘤细胞的增殖和对temozolomide的耐药性.
- MYH9通过招募USP14来抑制NAP1L1的无处不在和降解,从而导致NAP1L1的上调.
- 上调的NAP1L1激活了c-Myc,诱导了CCND1/CDK4的表达,并促进了增殖和化学抵抗.
- MYH9上调与质瘤患者的低生存率相关.
结论:
- MYH9通过调节NAP1L1二维基因化,驱动着质瘤的进展和特莫索洛米德耐药性.
- MYH9代表了改善质瘤治疗结果的潜在治疗标.
更多相关视频
07:48Utilizing Functional Genomics Screening to Identify Potentially Novel Drug Targets in Cancer Cell Spheroid Cultures
Published on: December 26, 2016
11.4K
11:32Identification of Transcription Factor Regulators using Medium-Throughput Screening of Arrayed Libraries and a Dual-Luciferase-Based Reporter
Published on: March 27, 2020
6.9K
相关概念视频
Abnormal Proliferation
4.6K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
4.6K
The Retinoblastoma Gene
4.1K
Tumor suppressor genes are normal genes that can slow down cell division, repair DNA mistakes, or program the cells for apoptosis in case of irreparable damage. Hence, they play an essential role in preventing the proliferation of damaged cells.
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
4.1K
