Laboratory of Experimental Oncology, Istituto Ortopedico Rizzoli, Via di Barbiano 1/10, 40136 Bologna, Italy.
Eur J Radiol. 2013 Dec;82(12):2115-23. doi: 10.1016/j.ejrad.2011.11.031. Epub 2011 Dec 23.
Sarcomas are a heterogeneous group of rare connective tissue tumors, representing 1% of adult and 15% of childhood cancers for which biological and pathological information is still incomplete. In bone tumors patients with metastatic disease at onset, those who relapse and those with post-surgical secondary lesions still have a dismal outcome because of poor response to current therapies. Different molecular biology approaches have identified activated cell signalling pathways or specific molecular endpoints that may be considered potential drug targets or markers useful for diagnosis/prognosis in musculoskeletal pathology. Recently, advances in the field of molecular imaging allow visualization of cell and metabolic functions with the use of targets that include cell membrane receptors, enzymes of intracellular transport. Moreover advanced non-invasive newer imaging techniques like 18-FDG PET, quantitative dynamic-contrast MR imaging, diffusion weighted imaging have all shown a potential in distinguish malignant from benign lesions, in revealing the efficacy of therapy in tumors, the onset of recurrence and a good reliability in reckoning the percentage of necrosis in Ewing sarcoma and osteosarcoma. Thus, in vivo detection of imaging cancer biomarkers may be useful to better characterize those complex pathologic processes, such as apoptosis, proliferation and angiogenesis that determine tumor aggressiveness, providing not only complementary information of prognostic metabolic indicators, but also data in real-time on the efficacy of the treatment through the modulation of the cell metabolism.
肉瘤是一组异质性罕见的结缔组织肿瘤,占成人肿瘤的 1%,儿童肿瘤的 15%,其生物学和病理学信息仍不完整。在骨肿瘤患者中,那些起始时就发生转移疾病、复发的患者和手术后发生继发性病变的患者,由于对现有治疗的反应不佳,预后仍然很差。不同的分子生物学方法已经确定了激活的细胞信号通路或特定的分子终点,这些可能被认为是肌肉骨骼病理学中潜在的药物靶点或有诊断/预后价值的标志物。最近,分子成像领域的进展使得可以使用包括细胞膜受体、细胞内转运酶在内的靶点来可视化细胞和代谢功能。此外,先进的新型非侵入性成像技术,如 18-FDG PET、定量动态对比磁共振成像、扩散加权成像,都显示出在区分良恶性病变、揭示肿瘤治疗效果、肿瘤复发的发生以及在 Ewing 肉瘤和骨肉瘤中准确估计坏死百分比方面具有潜力。因此,活体检测成像癌症生物标志物可能有助于更好地描述那些决定肿瘤侵袭性的复杂病理过程,如细胞凋亡、增殖和血管生成,不仅提供预后代谢指标的补充信息,还能通过调节细胞代谢提供治疗效果的实时数据。