从生物学到个性化医疗:骨肉瘤的最新知识

IF 1.6 4区 医学 Q3 GENETICS & HEREDITY
Audrey Mohr , Maria Eugenia Marques Da Costa , Olivia Fromigue , Baptiste Audinot , Thierno Balde , Robin Droit , Samuel Abbou , Pierre Khneisser , Pablo Berlanga , Esperanza Perez , Antonin Marchais , Nathalie Gaspar
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引用次数: 0

摘要

高级别骨肉瘤是最常见的儿童骨癌。采用目前的化疗和手术策略,三分之一以上的骨肉瘤患者会复发和死亡。要改善骨肉瘤的治疗效果,需要应对两个关键挑战:1-识别难以治疗的疾病,最好从诊断开始;2-选择最佳的联合或新型疗法,根除对当前疗法产生抗药性、导致疾病扩散和转移的肿瘤细胞及其有利的微环境。基因的混乱、肿瘤的复杂性和异质性使这项任务变得困难重重。新一代测序等新技术的发展提高了人们对骨肉瘤肿瘤发生的认识。本综述总结了骨肉瘤在生物学和治疗学方面的最新进展,以及为开发个性化药物和新的治疗策略并最终提高患者生存率而必须克服的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From biology to personalized medicine: Recent knowledge in osteosarcoma

High-grade osteosarcoma is the most common paediatric bone cancer. More than one third of patients relapse and die of osteosarcoma using current chemotherapeutic and surgical strategies. To improve outcomes in osteosarcoma, two crucial challenges need to be tackled: 1-the identification of hard-to-treat disease, ideally from diagnosis; 2- choosing the best combined or novel therapies to eradicate tumor cells which are resistant to current therapies leading to disease dissemination and metastasize as well as their favorable microenvironment. Genetic chaos, tumor complexity and heterogeneity render this task difficult. The development of new technologies like next generation sequencing has led to an improvement in osteosarcoma oncogenesis knownledge. This review summarizes recent biological and therapeutical advances in osteosarcoma, as well as the challenges that must be overcome in order to develop personalized medicine and new therapeutic strategies and ultimately improve patient survival.

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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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