Panczyszyn Elzbieta, Saverio Valentina, Monzani Romina, Gagliardi Mara, Petrovic Jelena, Stojkovska Jasmina, Collavin Licio, Corazzari Marco
Department of Health Sciences and Center for Translational Research on Autoimmune and Allergic Disease (CAAD), University of Piemonte Orientale, Novara, Italy.
Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Piemonte Orientale, Novara, Italy.
Cell Death Discov. 2024 Feb 17;10(1):87. doi: 10.1038/s41420-024-01854-2.
Human osteosarcoma (OS) is a relatively rare malignancy preferentially affecting long body bones which prognosis is often poor also due to the lack of effective therapies. Clinical management of this cancer basically relies on surgical removal of primary tumor coupled with radio/chemotherapy. Unfortunately, most osteosarcoma cells are resistant to conventional therapy, with the undergoing epithelial-mesenchymal transition (EMT) giving rise to gene expression reprogramming, thus increasing cancer cell invasiveness and metastatic potential. Alternative clinical approaches are thus urgently needed. In this context, the recently described ferroptotic cell death represents an attractive new strategy to efficiently kill cancer cells, since most chemoresistant and mesenchymal-shaped tumors display high susceptibility to pro-ferroptotic compounds. However, cancer cells have also evolved anti-ferroptotic strategies, which somehow sustain their survival upon ferroptosis induction. Indeed, here we show that osteosarcoma cell lines display heterogeneous sensitivity to ferroptosis execution, correlating with the mesenchymal phenotype, which is consistently affected by the expression of the well-known anti-ferroptotic factor ferroptosis suppressor protein 1 (FSP1). Interestingly, inhibiting the activity or expression of FSP1 restores cancer cell sensitivity to ferroptosis. Moreover, we also found that: i) AKRs might also contribute to resistance; ii) NRF2 enhances FSP1 expression upon ferroptosis induction; while iii) p53 contributes to the regulation of FSP1 basal expression in OS cells.In conclusion, FSP1 expression can potentially be used as a valuable predictive marker of OS sensitivity to ferroptosis and as a new potential therapeutic target.
人类骨肉瘤(OS)是一种相对罕见的恶性肿瘤,主要影响长骨,由于缺乏有效的治疗方法,其预后往往很差。这种癌症的临床管理主要依赖于手术切除原发性肿瘤并结合放疗/化疗。不幸的是,大多数骨肉瘤细胞对传统治疗具有抗性,经历上皮-间质转化(EMT)会导致基因表达重编程,从而增加癌细胞的侵袭性和转移潜力。因此,迫切需要替代的临床方法。在这种背景下,最近描述的铁死亡细胞死亡代表了一种有吸引力的有效杀死癌细胞的新策略,因为大多数化疗耐药和间充质形态的肿瘤对促铁死亡化合物表现出高度敏感性。然而,癌细胞也进化出了抗铁死亡策略,这在某种程度上维持了它们在铁死亡诱导后的存活。事实上,我们在此表明骨肉瘤细胞系对铁死亡执行表现出异质性敏感性,这与间充质表型相关,而间充质表型始终受到著名的抗铁死亡因子铁死亡抑制蛋白1(FSP1)表达的影响。有趣的是,抑制FSP1的活性或表达可恢复癌细胞对铁死亡的敏感性。此外,我们还发现:i)醛酮还原酶(AKRs)也可能导致抗性;ii)核因子E2相关因子2(NRF2)在铁死亡诱导后增强FSP1表达;而iii)p53有助于调节骨肉瘤细胞中FSP1的基础表达。总之,FSP1表达有可能用作骨肉瘤对铁死亡敏感性的有价值预测标志物和新的潜在治疗靶点。