尤文肉瘤的生物学特性。

ISRN oncology Pub Date : 2013-01-01 Epub Date: 2013-01-10 DOI:10.1155/2013/759725
Keir A Ross, Niall A Smyth, Christopher D Murawski, John G Kennedy
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引用次数: 0

摘要

研究目的本研究的目的是回顾目前有关尤文氏肉瘤生物学的文献,包括目前的治疗方法以及了解生物学机制对未来治疗产生影响的途径。研究方法对 PubMed 和 Cochrane Collaboration 进行了检索。临床前和临床证据均在考虑之列,但具体病例报告不在考虑之列。对主要研究文章和综述进行了分析,重点是近期发表的文章。研究结果尤文肉瘤与特定的染色体易位和由此产生的转录本/蛋白有关。有关尤文肉瘤生物学的知识不断增加,但尚未对新疗法产生重大影响或产生新疗法。局部病例的存活率有所提高,但转移和复发病例的存活率却不尽相同。标准手术、放疗和化疗的疗效已达到极限。结论改善预后的关键可能在于推进生物标志物和早期诊断,确定起源细胞,以及开发有效的分子疗法和抗血管生成药物。临床前证据表明,分子疗法可用于尤文肉瘤。早期临床结果也揭示了新型疗法的潜力,但还需要进一步的开发和评估才能推广应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The biology of ewing sarcoma.

Objective. The goal of this study was to review the current literature on the biology of Ewing's sarcoma, including current treatments and the means by which an understanding of biological mechanisms could impact future treatments. Methods. A search of PubMed and The Cochrane Collaboration was performed. Both preclinical and clinical evidence was considered, but specific case reports were not. Primary research articles and reviews were analyzed with an emphasis on recent publications. Results. Ewing sarcoma is associated with specific chromosomal translocations and the resulting transcripts/proteins. Knowledge of the biology of Ewing sarcoma has been growing but has yet to significantly impact or produce new treatments. Localized cases have seen improvements in survival rates, but the same cannot be said of metastatic and recurrent cases. Standard surgical, radiation, and chemotherapy treatments are reaching their efficacy limits. Conclusion. Improving prognosis likely lies in advancing biomarkers and early diagnosis, determining a cell(s) of origin, and developing effective molecular therapeutics and antiangiogenic agents. Preclinical evidence suggests the utility of molecular therapies for Ewing sarcoma. Early clinical results also reveal potential for novel treatments but require further development and evaluation before widespread use can be advocated.

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