DNA甲基转移酶DNMT3A抑制TP53AIP1的表达,并促进子宫癌的发展和转移
Xiaohong Pan1, Xiuluan Du2, Suhong Jia1
1Department of Gynecology and Obstetrics, The Second Affiliated Hospital of Soochow University, No. 1055#, Sanxiang Road, Gusu District, Suzhou, 215004 Jiangsu P. R. China.
Cytotechnology
|March 10, 2025
概括
DNA甲基转移酶3A (DNMT3A) 通过抑制TP53AIP1的表达,促进子宫癌 (CC) 的进展和转移. 恢复TP53AIP1激活了p53信号,抑制了癌细胞的生长和转移.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 癌症遗传学 癌症遗传学
背景情况:
- 宫癌 (CC) 的预后不好,复发率和转移率很高.
- 确定驱动CC进展的关键基因对于治疗开发至关重要.
研究的目的:
- 为了研究枢纽基因在宫癌进展中的作用.
- 阐明TP53AIP1的调节机制及其对CC恶性瘤的影响.
主要方法:
- 对GSE9750数据集的生物信息分析.
- 在体外测试 (CCK-8,殖民地形成,EDU,TUNEL,Transwell) 和西布洛特.
- 在体内转移的测定.
- 监管机制调查的双化酶,ChIP和MSP测定.
主要成果:
- 发现TP53AIP1在CC组织和细胞系中的下调.
- 通过p53信号传递,TP53AIP1过度表达抑制了CC细胞的增殖,迁移,入侵和诱导的亡.
- DNMT3A直接抑制了TP53AIP1的转录;DNMT3A沉默抑制了CC的发展和转移,这种效应被TP53AIP1的淘汰扭转.
结论:
- 通过转录抑制TP53AIP1.1,DNMT3A促进子宫癌的进展和转移.
- TP53AIP1通过激活p53-介导的亡,作为一种瘤抑制剂.
- 针对DNMT3A/TP53AIP1轴可能为宫癌提供治疗策略.
相关概念视频
Abnormal Proliferation
4.4K
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...
4.4K
DNA Damage can Stall the Cell Cycle
9.0K
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
9.0K
Negative Regulator Molecules
35.1K
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
35.1K
Epigenetic Regulation
3.0K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
3.0K
Loss of Tumor Suppressor Gene Functions
4.7K
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.
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
4.7K
piRNA - Piwi-interacting RNAs
6.7K
PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
6.7K


