通过DUSP16介导的MAPK/AMPK通路激活,SBEM在乳腺癌中赋予了帕克利塔塞尔耐药性
Liang Liu1, Ning Lu2, Xiaomei Liu3
1Graduate School, Xinjiang Medical University, Urumqi, Xinjiang Uygur Autonomous Region 830000, P.R. China.
Oncology letters
|November 3, 2025
概括
小乳腺上皮质粘素 (SBEM) 通过激活AMPK通路和调节DUSP16. 减少SBEM可以恢复耐药乳腺癌细胞对化疗的敏感性.
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:
- 小乳腺上皮质粘素 (SBEM) 在乳腺瘤和淋巴结中被上调.
- SBEM涉及化学抵抗,并被确定为微转移的潜在生物标志物.
- 通过SBEM介导的化学抵抗的分子机制尚未完全理解.
研究的目的:
- 阐明SBEM调节乳腺癌中帕克利塔塞尔 (PTX) 耐药性的机制.
- 研究AMPK途径在SBEM介导效应中的作用.
- 探索SBEM和DUSP16之间的相互作用.
主要方法:
- 开发了具有SBEM过度表达和敲击的乳腺癌细胞系.
- 使用AMPK激活器 (13) 来研究途径参与.
- 评估了细胞活力,细胞亡和PTX敏感性.
主要成果:
- 过度表达SBEM增加了乳腺癌细胞活力和PTX耐药性.
- 在SBEM knockdown中,增强了亡并恢复了耐药细胞中的PTX敏感性.
- 发现SBEM与DUSP16相互作用并对其进行上调,抑制AMPK信号传递.
结论:
- 通过增强DUSP16表达和激活AMPK信号通路,SBEM在乳腺癌中赋予PTX抗性.
- 异常的AMPK通路激活有助于PTX耐药性.
- 准SBEM或AMPK通路可以克服化学抵抗.
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