在临床试验中应用蛋白质组学:评估卵巢癌的潜力和实际局限性。

Nana E Tchabo, Meghan S Liel, Elise C Kohn
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引用次数: 9

摘要

卵巢癌是美国妇女妇科恶性肿瘤死亡的主要原因,也是欧洲和美国妇女癌症死亡的第四大常见原因。尽管进行了适当的手术和化疗干预,但转移性癌症患者的5年生存率仍然很低。目前可用的筛查方法,包括CA125、其他生物标志物和经阴道超声,缺乏必要的敏感性和特异性,无法为普通人群提供准确和经济有效的筛查,也无法评估谁将从每种治疗中获益最多。这些局限性促使蛋白质组学技术的研究及其在卵巢癌诊断中的应用。蛋白质组学是研究正常或患病状态下功能蛋白通路中的分子。目前正在进行临床试验,以评估血清蛋白质组学模式的敏感性和特异性,并设计其他临床试验,以评估分子靶向药物对人类受试者蛋白质信号通路的影响。克服科学和实践上的限制,将增加对癌细胞中紊乱的蛋白质网络的了解。蛋白质组学的临床试验可能会改善早期检测,更好的监测,新药和分子靶向治疗,以及个性化治疗。
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Applying proteomics in clinical trials: assessing the potential and practical limitations in ovarian cancer.

Ovarian cancer is the leading cause of death from gynecologic malignancies among American women and the fourth most frequent cause of death from cancer in women in Europe and the US. Despite appropriate surgical and chemotherapeutic intervention, the 5-year survival in patients with metastatic cancer remains poor. Currently available screening methods, including CA125, additional biomarkers, and transvaginal ultrasound lack the necessary sensitivity and specificity to provide accurate and cost-efficient screening for the general population or the ability to assess who will benefit most from each treatment. These limitations have prompted the study of proteomic technology and its application in ovarian cancer diagnostics. Proteomics is the study of molecules in the functional protein pathways of normal or diseased states. Clinical trials are currently being conducted to assess the sensitivity and specificity of serum proteomic patterns and additional clinical trials are designed to evaluate the effects of molecularly targeted agents on protein signaling pathways in human subjects. Overcoming both scientific and practical limitations will lead to increased knowledge of deranged protein networks in cancer cells. Clinical trials in proteomics may result in improved early detection, better monitoring, new drugs and molecularly targeted therapeutics, and individualized therapies.

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