Pandey Surya Nath, Babu M Arockia, Ali Haider, H Malathi, Maharana Laxmidhar, Goyal Kavita, Rana Mohit, Imran Mohd
Department of Pharmacology, Teerthanker Mahaveer College of Pharmacy, Teerthanker Mahaveer University, Moradabad 244001 Uttar Pradesh, India.
Institute of Pharmaceutical Research, GLA UNIVERSITY, Mathura, UP 281406, India.
Clin Chim Acta. 2025 Aug 15;576:120387. doi: 10.1016/j.cca.2025.120387. Epub 2025 May 25.
Breast cancer remains the leading cause of cancer mortality in women, and early detection coupled with real-time monitoring of tumor burden are clinical imperatives; yet existing imaging-based screening (e.g., mammography, ultrasound) suffers from sensitivities as low as 60-80% and even lower in dense breasts plus substantial false-positive rates, underscoring the critical need for molecular assays with higher accuracy. Current clinical assays for circulating MUC1 (CA15-3) achieve high specificity but exhibit limited sensitivity in early-stage disease, underscoring a critical unmet need for more sensitive, multiplexed biomarkers to enable timely intervention. Mass spectrometry-based glycoproteomic workflows offer multiplexed quantification of tumour-associated MUC1 glycoforms, substantially improving analytical specificity and dynamic range. Complementary liquid-biopsy platforms that detect anti-MUC1 autoantibodies further extend lead time for recurrence detection. Concurrently, small interfering RNA (siRNA) therapies targeting MUC1 delivered via ionizable lipid nanoparticles demonstrate efficient tumor accumulation, robust mRNA knockdown, and favourable safety in phaseI solid tumor trials. In this review, we critically assess the analytical performance and standardization challenges of current MUC1 assays, evaluate emerging mass spectrometry and immunoarray techniques, and examine chemical and nanocarrier strategies that surmount biological barriers to siRNA delivery. We propose a co-development framework for harmonized companion diagnostics and MUC1-directed RNAi therapeutics under unified regulatory pathways, paving the way for precision, biomarker-driven interventions in breast cancer care.
乳腺癌仍然是女性癌症死亡的主要原因,早期检测以及对肿瘤负荷的实时监测是临床的当务之急;然而,现有的基于成像的筛查方法(如乳腺X线摄影、超声检查)的灵敏度低至60%-80%,在致密型乳腺中甚至更低,且假阳性率很高,这突出表明迫切需要更高准确性的分子检测方法。目前用于循环MUC1(CA15-3)的临床检测方法具有高特异性,但在疾病早期阶段的灵敏度有限,这突出表明迫切需要更敏感的多重生物标志物以实现及时干预。基于质谱的糖蛋白质组学工作流程可对肿瘤相关的MUC1糖型进行多重定量,大大提高了分析特异性和动态范围。检测抗MUC1自身抗体的补充性液体活检平台进一步延长了复发检测的提前期。同时,通过可电离脂质纳米颗粒递送的靶向MUC1的小干扰RNA(siRNA)疗法在I期实体瘤试验中显示出有效的肿瘤蓄积、强大的mRNA敲低效果和良好的安全性。在本综述中,我们批判性地评估了当前MUC1检测方法的分析性能和标准化挑战,评估了新兴的质谱和免疫阵列技术,并研究了克服siRNA递送生物屏障的化学和纳米载体策略。我们提出了一个共同开发框架,用于在统一监管途径下协调伴随诊断和MUC1导向的RNAi疗法,为乳腺癌护理中精准的、基于生物标志物的干预措施铺平道路。