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尤因肉瘤病理生物学的最新进展

Latest developments in the pathobiology of Ewing sarcoma.

作者信息

Karlina Irina, Schroeder Brett A, Kirgizov Kirill, Romantsova Olga, Istranov Andrey L, Nedorubov Andrey, Timashev Peter, Ulasov Ilya

机构信息

Group of Experimental Biotherapy and Diagnostics, Institute for Regenerative Medicine, World-Class Research Centre "Digital Biodesign and Personalized Healthcare", I.M. Sechenov First Moscow State Medical University, Moscow 119991, Russia.

National Cancer Institute, National Institutes of Health, Bethesda, MD 20814, USA.

出版信息

J Bone Oncol. 2022 Jul 1;35:100440. doi: 10.1016/j.jbo.2022.100440. eCollection 2022 Aug.

Abstract

Ewing's sarcoma (ES) is an aggressive malignant tumor commonly affecting adolescents. The standard of care includes surgical treatment and systemic therapies, although ES patients often develop drug resistance, leading to disease progression. Tumorigenesis in Ewing's sarcoma has unique characteristics that allow for the development of targeted therapeutics. New data on the role of oncogenic drivers in ES tumorigenesis, particularly in relation to treatment-induced stress, offers new therapeutic opportunities. This review summarizes the latest information on the clinically relevant oncogenes found in Ewing's sarcoma, their biological roles, and candidate targets for improving ES patient outcomes.

摘要

尤因肉瘤(ES)是一种侵袭性恶性肿瘤,常见于青少年。尽管ES患者常出现耐药性导致疾病进展,但治疗标准仍包括手术治疗和全身治疗。尤因肉瘤的肿瘤发生具有独特特征,这使得靶向治疗成为可能。关于致癌驱动因素在ES肿瘤发生中的作用的新数据,特别是与治疗引起的应激相关的数据,提供了新的治疗机会。本综述总结了尤因肉瘤中发现的临床相关致癌基因的最新信息、它们的生物学作用以及改善ES患者预后的候选靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6bd/9287185/395a22a45548/gr1.jpg

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