Josie A Christopher, Lisa M Breckels, Oliver M Crook, Mercedes Vazquez-Chantada, Derek Barratt, Kathryn Susan Lilley
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引用次数: 0
摘要
细胞通过表达、翻译后修饰和亚细胞定位的分子变化,对本底水平的电离辐射(IR)具有多种保护机制。肿瘤学中的放射治疗试图压制这些机制,但放射抗性是一个持续的挑战。在这里,全局亚细胞蛋白质组学与贝叶斯建模相结合,确定了 A549 细胞在 6 Gy X 射线照射下 544 个不同定位的蛋白质,揭示了参与铁凋亡(一种依赖铁的细胞死亡)的蛋白质的亚细胞特异性变化,提示了潜在的放射抗性机制。这些观察结果与表达变化无关,强调了全局亚细胞蛋白质组学的实用性,以及诱导铁蛋白沉积以对抗放射抗性的疗法的广阔前景。
Global proteomics indicates subcellular-specific anti-ferroptotic responses to ionizing radiation
Cells have many protective mechanisms against background levels of ionizing radiation (IR) orchestrated by molecular changes in expression, post-translation modifications and subcellular localization. Radiotherapeutic treatment in oncology attempts to overwhelm such mechanisms, but radio-resistance is an ongoing challenge. Here, global subcellular proteomics combined with Bayesian modelling identified 544 differentially localized proteins in A549 cells upon 6 Gy x-ray exposure, revealing subcellular-specific changes of proteins involved in ferroptosis, an iron-dependent cell death, suggestive of potential radio-resistance mechanisms. These observations were independent of expression changes, emphasizing the utility of global subcellular proteomics and the promising prospect of ferroptosis-inducing therapies for combatting radioresistance.