Rathore Richa, Van Tine Brian A
Division of Medical Oncology, Washington University in St. Louis, St. Louis, MO 63110, USA.
Division of Pediatric Hematology and Oncology, St. Louis Children's Hospital, St. Louis, MO 63110, USA.
J Clin Med. 2021 Mar 12;10(6):1182. doi: 10.3390/jcm10061182.
Osteosarcoma is the most common primary malignant bone tumor in children and young adults. The standard-of-care curative treatment for osteosarcoma utilizes doxorubicin, cisplatin, and high-dose methotrexate, a standard that has not changed in more than 40 years. The development of patient-specific therapies requires an in-depth understanding of the unique genetics and biology of the tumor. Here, we discuss the role of normal bone biology in osteosarcomagenesis, highlighting the factors that drive normal osteoblast production, as well as abnormal osteosarcoma development. We then describe the pathology and current standard of care of osteosarcoma. Given the complex heterogeneity of osteosarcoma tumors, we explore the development of novel therapeutics for osteosarcoma that encompass a series of molecular targets. This analysis of pathogenic mechanisms will shed light on promising avenues for future therapeutic research in osteosarcoma.
骨肉瘤是儿童和青年中最常见的原发性恶性骨肿瘤。骨肉瘤的标准治疗方案采用阿霉素、顺铂和大剂量甲氨蝶呤,这一标准40多年来一直未变。开发针对特定患者的疗法需要深入了解肿瘤独特的遗传学和生物学特性。在此,我们讨论正常骨生物学在骨肉瘤发生中的作用,重点介绍驱动正常成骨细胞生成以及异常骨肉瘤发展的因素。然后,我们描述骨肉瘤的病理学和当前的治疗标准。鉴于骨肉瘤肿瘤具有复杂的异质性,我们探索针对骨肉瘤的新型治疗方法,这些方法涵盖了一系列分子靶点。对致病机制的分析将为骨肉瘤未来治疗研究的有前景途径提供线索。