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在MTA1和MTA3/TRIM21之间的反循环调节乳腺癌的干性,以应对雌激素
Jingyao Zhang1, Yinuo Wang1, Jingjing Zhang1
1State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cell death & disease
|August 17, 2024
概括
转移关联蛋白1 (MTA1) 通过抑制瘤抑制剂MTA3和TRIM21驱动乳腺癌的进展. 雌激素破坏了这种平衡,影响了癌症干和EMT,突出了MTA1作为治疗点.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 转移相关蛋白 (MTA) 家族与乳腺癌的发展有关.
- 乳腺癌进展中MTA家族成员的机制尚不清楚.
研究的目的:
- 研究MTA1,MTA3和TRIM21在乳腺癌扩散,入侵,EMT和干性中的作用.
- 在MTA1,MTA3和TRIM21之间解雌激素调节的反循环.
主要方法:
- 在体内和体外乳腺癌细胞模型.
- 染色体免疫沉 (ChIP) 和光酶记者测定.
- 免疫沉 (IP) 和无处不在的测试.
主要成果:
- 通过抑制瘤抑制基因MTA3和TRIM21.1,MTA1促进乳腺癌的发生.
- MTA3 抑制了 MTA1 的转录;TRIM21 调节了 MTA1 蛋白质的稳定性.
- 雌激素会破坏MTA1/MTA3和MTA1/TRIM21的平衡,影响茎状和EMT.
结论:
- MTA1是乳腺癌干细胞命运和EMT通过MTA3/TRIM21.21反循环的关键调节者.
- MTA1,MTA3和TRIM21显示出作为预后生物标志物的潜力.
- MTA1代表了乳腺癌的一个有前途的治疗标.
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