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铁死亡与口腔鳞状细胞癌:梳理脉络,砥砺前行。

Ferroptosis and oral squamous cell carcinoma: connecting the dots to move forward.

作者信息

Antonelli Alessandro, Battaglia Anna Martina, Sacco Alessandro, Petriaggi Lavinia, Giorgio Emanuele, Barone Selene, Biamonte Flavia, Giudice Amerigo

机构信息

Department of Health Science, School of Dentistry, "Magna Graecia" University of Catanzaro, Catanzaro, Italy.

Laboratory of Biochemistry and Cellular Biology, Department of Experimental and Clinical Medicine, "Magna Graecia" University of Catanzaro, Catanzaro, Italy.

出版信息

Front Oral Health. 2024 Sep 4;5:1461022. doi: 10.3389/froh.2024.1461022. eCollection 2024.

Abstract

Oral squamous cell carcinoma (OSCC) is an aggressive disease whose incomplete biological comprehension contributes to the inappropriate clinical management and poor prognosis. Thus, the identification of new promising molecular targets to treat OSCC is of paramount importance. Ferroptosis is a regulated cell death caused by the iron-dependent accumulation of reactive oxygen species and the consequent oxidative damage of lipid membranes. Over the last five years, a growing number of studies has reported that OSCC is sensitive to ferroptosis induction and that ferroptosis inducers exert a remarkable antitumor effect in OSCC, even in those displaying low response to common approaches, such as chemotherapy and radiotherapy. In addition, as ferroptosis is considered an immunogenic cell death, it may modulate the immune response against OSCC. In this review, we summarize the so far identified ferroptosis regulatory mechanisms and prognostic models based on ferroptosis-related genes in OSCC. In addition, we discuss the perspective of inducing ferroptosis as a novel strategy to directly treat OSCC or, alternatively, to improve sensitivity to other approaches. Finally, we integrate data emerging from the research studies, reviewed here, through in silico analysis and we provide a novel personal perspective on the potential interconnection between ferroptosis and autophagy in OSCC.

摘要

口腔鳞状细胞癌(OSCC)是一种侵袭性疾病,对其生物学理解的不完整导致了不恰当的临床管理和不良预后。因此,确定有前景的治疗OSCC的新分子靶点至关重要。铁死亡是一种由铁依赖性活性氧积累和随之而来的脂质膜氧化损伤引起的程序性细胞死亡。在过去五年中,越来越多的研究报告称,OSCC对铁死亡诱导敏感,铁死亡诱导剂在OSCC中发挥显著的抗肿瘤作用,即使是那些对化疗和放疗等常见方法反应较低的肿瘤。此外,由于铁死亡被认为是一种免疫原性细胞死亡,它可能会调节针对OSCC的免疫反应。在这篇综述中,我们总结了目前已确定的OSCC中铁死亡调节机制和基于铁死亡相关基因的预后模型。此外,我们讨论了诱导铁死亡作为直接治疗OSCC或提高对其他治疗方法敏感性的新策略的前景。最后,我们通过计算机分析整合了本文综述的研究中出现的数据,并就OSCC中铁死亡与自噬之间的潜在相互联系提供了新颖的个人观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08d1/11408306/610705b5bf57/froh-05-1461022-g001.jpg

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