University Hospital Freiburg, Center for Pediatrics and Adolescent Medicine, Clinic IV: Pediatric Hematology and Oncology, Mathildenstr. 1, 79106 Freiburg , Germany +49 761 270 43000 ; +49 761 270 45180 ;
Expert Opin Drug Discov. 2011 Oct;6(10):1103-25. doi: 10.1517/17460441.2011.611498. Epub 2011 Sep 6.
Rhabdomyosarcomas (RMS) are rare heterogeneous pediatric tumors that are treated by surgery, chemotherapy and irradiation. New therapeutic approaches are needed, especially in the advanced stages to target the pro-oncogenic signals. Exploring the molecular interactions of the regulatory signals and their roles in the developmental aspects of different subtypes of RMS is essential to identify potential targets and develop new therapeutic drugs.
Insights into different drug discovery approaches are discussed with specific emphasis on gene expression profiling, fusion protein, role of small interfering RNA (siRNA)- and microRNA (miRNA)-based discovery approaches, targeting cancer stem cells, and in vitro and in vivo model systems. Targeting some overexpressed signals along with the possibilities of combination therapy of validated drug targets is discussed. Additionally, methods to overcome the limitations of discovery-based research are briefly discussed.
Due to drug resistance, ineffective therapy in advanced stages and relapse, there is a demand to explore new drug targets and discovery approaches. Implementing miRNA-based profiling would reveal the extent of miR-based regulation, various biomarkers and potential targets in RMS. A suitable combination of innovative techniques and the use of model systems might assist the identification and validation of novel targets and drug discovery methods. Combining specific drugs along with type-specific target inhibition of overexpressed mRNAs through siRNA approaches would enable the development of personalized therapy.
横纹肌肉瘤(RMS)是一种罕见的异质性儿科肿瘤,通过手术、化疗和放疗进行治疗。需要新的治疗方法,特别是在晚期阶段,以针对致癌信号。探索调节信号的分子相互作用及其在不同 RMS 亚型发育方面的作用对于确定潜在靶点和开发新的治疗药物至关重要。
讨论了不同的药物发现方法的见解,特别强调了基因表达谱分析、融合蛋白、基于小干扰 RNA(siRNA)和 microRNA(miRNA)的发现方法、针对癌症干细胞的作用,以及体外和体内模型系统。讨论了针对一些过表达信号的可能性,以及验证药物靶点的联合治疗的可能性。此外,还简要讨论了克服发现研究局限性的方法。
由于耐药性、晚期治疗无效和复发,有必要探索新的药物靶点和发现方法。实施基于 miRNA 的分析将揭示 RMS 中基于 miR 的调节、各种生物标志物和潜在靶点的程度。创新技术的适当组合以及模型系统的使用可能有助于鉴定和验证新的靶点和药物发现方法。通过 siRNA 方法结合特定药物和针对过表达 mRNA 的特定靶点抑制,可实现个性化治疗的发展。