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振荡性低氧诱导的未折叠蛋白质折叠反应基因表达预测人类乳腺癌患者的低生存率
bioRxiv : the preprint server for biology
|February 8, 2024
概括
振荡性缺氧,与稳定性缺氧不同,改变基因表达并诱导未折叠的蛋白质反应,影响癌症恶性和患者的存活率. 这一发现对于了解三阴性乳腺癌进展至关重要.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 缺氧是瘤微环境中的关键因素,影响癌症转移.
- 瘤缺氧可能是动态的,氧气水平波动或振荡.
- 转录因子HIF-1是细胞对低氧反应的关键调节者.
研究的目的:
- 研究振荡性缺氧对三阴性乳腺癌中基因表达的特定影响.
- 为了比较由振荡性缺氧和稳定性缺氧引起的基因表达变化.
- 为了确定在人类癌症中振荡性缺氧诱导的基因表达特征的临床相关性.
主要方法:
- 利用MDA-MB-231细胞,这是三阴性乳腺癌与严重缺氧的模型.
- 在振荡性缺氧条件下测量基因表达的变化.
- 分析了人类癌症样本的癌症基因组图谱 (TCGA) RNAseq数据.
主要成果:
- 与稳定的缺氧相比,振荡性缺氧会诱导不同的基因表达模式,有时会产生相反的效果.
- 一个振荡性缺氧特异性的基因表达特征在大多数人类癌症中得到了丰富.
- 这种特征与乳腺癌患者的生存结果较差有关.
结论:
- 振荡性缺氧独特地影响基因表达和细胞反应,包括未折叠蛋白质反应 (UPR).
- 由振荡性缺氧引起的UPR与乳腺癌的存活率降低有关.
- 了解动态缺氧对于开发向癌症疗法至关重要.
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