Savas Irem Nur, Coskun Abdurrahman
Department of Biochemistry and Molecular Biology, Institute of Health Sciences, Acibadem Mehmet Ali Aydinlar University, Istanbul 34752, Turkey.
Department of Medical Biochemistry, School of Medicine, Acibadem Mehmet Ali Aydinlar University, Kayisdagi cad., No: 32, Istanbul 34752, Turkey.
Biomolecules. 2025 Jul 14;15(7):1011. doi: 10.3390/biom15071011.
Malignant diseases represent a major global health challenge and are among the leading causes of death worldwide. Accurate early diagnosis is essential for improving outcomes and combating these conditions effectively. Currently, the diagnosis of malignancies relies heavily on radiological imaging and pathological examinations, which are often invasive and not cost-effective. As such, there is a growing need for non-invasive and accessible methods to detect cancer in its early stages. Tumor markers-biomolecules whose levels increase in malignancy and can be measured in blood or other biological tissues and fluids-offer a promising tool. However, the sensitivity and specificity of currently available tumor markers are insufficient for early detection, limiting their use primarily to disease monitoring rather than diagnosis. While ongoing research continues to identify novel tumor markers, the development of more effective early detection strategies requires more than the discovery of new biomarkers. The continuous monitoring of patients and individuals with a high tumor risk and the personalization of tumor marker interpretation are also critical. In this review, we (i) summarize the most commonly used tumor markers, (ii) examine strategies for developing novel biomarkers, particularly through omics technologies, (iii) explore the potential of continuous monitoring using wearable biosensors for early tumor detection, and (iv) discuss approaches to personalizing tumor marker interpretation to support early diagnosis and improve treatment outcomes.
恶性疾病是全球主要的健康挑战之一,也是全球主要死因。准确的早期诊断对于改善治疗结果和有效对抗这些疾病至关重要。目前,恶性肿瘤的诊断严重依赖于放射影像学和病理检查,而这些检查往往具有侵入性且成本效益不高。因此,越来越需要非侵入性且易于获得的方法来早期检测癌症。肿瘤标志物——其水平在恶性肿瘤中升高且可在血液或其他生物组织及体液中测量的生物分子——提供了一种有前景的工具。然而,目前可用的肿瘤标志物的敏感性和特异性不足以用于早期检测,主要将其用途限制在疾病监测而非诊断上。虽然正在进行的研究不断发现新的肿瘤标志物,但开发更有效的早期检测策略需要的不仅仅是发现新的生物标志物。对肿瘤高风险患者和个体的持续监测以及肿瘤标志物解释的个性化也至关重要。在本综述中,我们(i)总结最常用的肿瘤标志物,(ii)研究开发新型生物标志物的策略,特别是通过组学技术,(iii)探索使用可穿戴生物传感器进行持续监测以早期检测肿瘤的潜力,以及(iv)讨论使肿瘤标志物解释个性化以支持早期诊断和改善治疗结果的方法。