胰腺癌
生物标志物
聚糖
癌症研究
糖基化
单克隆抗体
癌症
计算生物学
生物标志物发现
癌症生物标志物
生物
医学
聚唾液酸
腺癌
唾液酸
胰腺
连接器
小RNA
胰腺疾病
生物信息学
抗原
微泡
癌细胞
胰岛素瘤
转移
靶向治疗
作者
Lingrui Huang,Song Gao,Qi Li,Fang Jin,Anqi Zhang,Xiawen Lin,Yanrong Wen,Wenyan Guan,Jie Shen,Jian He,Zhen Liu
标识
DOI:10.1073/pnas.2611747123
摘要
Pancreatic cancer remains one of the most lethal malignancies, largely due to the lack of reliable biomarkers for early detection. Aberrant glycosylation presents a promising source of diagnostic signatures, yet polysialic acid (polySia), a distinctive glycan, has remained underexplored, primarily owing to limitations in detection methods and recognition tools. Here, we report the development of a polySia "superbinder," a nanoscale molecularly imprinted polymer (nanoMIP) that exhibits superior specificity and affinity for polySia over monoclonal antibodies, enabling precise recognition and quantification of this glycan. Leveraging this superbinder, we uncover a previously unrecognized association between polySia and pancreatic cancer and establish polysialylated CD56 (polySia-CD56) as a specific and robust biomarker. PolySia-CD56 outperforms multiple previously reported pancreatic cancer biomarkers, including the clinical standard carbohydrate antigen 19-9 (CA19-9). Notably, its expression pattern is complementary to that of CA19-9, and the combined use of both biomarkers significantly enhances diagnostic accuracy to 94.1%, effectively addressing the limitation of CA19-9 in detecting CA19-9-negative patients. Together, this study not only identifies polySia-CD56 as a precise biomarker for pancreatic cancer but also highlights the potential of antiglycan nanoMIPs as transformative reagents for decoding glycosylated targets and advancing clinical translation.
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