Balaraman Ashok Kumar, Moglad Ehssan, Afzal Muhammad, Babu M Arockia, Goyal Kavita, Roopashree R, Kaur Irwanjot, Kumar Sachin, Kumar MRavi, Chauhan Ashish Singh, Hemalatha S, Gupta Gaurav, Ali Haider
Research and Enterprise, University of Cyberjaya, Persiaran Bestari, Cyber 11, Cyberjaya, Selangor 63000, Malaysia.
Department of Pharmaceutics, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Al Kharj 11942, Saudi Arabia.
Clin Chim Acta. 2025 Feb 1;567:120105. doi: 10.1016/j.cca.2024.120105. Epub 2024 Dec 18.
Pancreatic cancer is a highly fatal malignancy due to poor early detection rate and resistance to conventional therapies. This review examines the potential for liquid biopsy as a transformative technology to identify diagnostic and therapeutic targets in pancreatic cancer. Specifically, we explore emerging biomarkers such as exosomal non-coding RNAs (ncRNAs), circulating tumor DNA (ctDNA), and circulating tumor cells (CTCs). Tumor-derived exosomes contain nucleic acid and protein that reflect the unique molecular landscape of the malignancy and can serve as an alternative diagnostic approach vs traditional biomarkers like CA19-9. Herein we highlight exosomal miRNAs, lncRNAs, and other ncRNAs alongside ctDNA and CTC-based strategies, evaluating their combined ability to improve early detection, disease monitoring and treatment response. Furthermore, the therapeutic implications of ncRNAs such as lncRNA UCA1 and miR-3960 in chemoresistance and progression are also discussed via suppression of EZH2 and PTEN/AKT pathways. Emerging therapeutic strategies that target the immune response, epithelial-mesenchymal transition (EMT) and drug resistance are explored. This review demonstrates a paradigm shift in pancreatic cancer management toward personalized, less invasive and more effective approaches.
由于早期检测率低以及对传统疗法耐药,胰腺癌是一种高度致命的恶性肿瘤。本综述探讨了液体活检作为一种变革性技术在识别胰腺癌诊断和治疗靶点方面的潜力。具体而言,我们探索了诸如外泌体非编码RNA(ncRNAs)、循环肿瘤DNA(ctDNA)和循环肿瘤细胞(CTCs)等新兴生物标志物。肿瘤来源的外泌体含有反映恶性肿瘤独特分子格局的核酸和蛋白质,与CA19-9等传统生物标志物相比,可作为一种替代诊断方法。在此,我们重点介绍外泌体miRNAs、lncRNAs和其他ncRNAs以及基于ctDNA和CTCs的策略,评估它们在改善早期检测、疾病监测和治疗反应方面的综合能力。此外,还通过抑制EZH2和PTEN/AKT途径讨论了lncRNA UCA1和miR-3960等ncRNAs在化疗耐药和进展中的治疗意义。探索了针对免疫反应、上皮-间质转化(EMT)和耐药性的新兴治疗策略。本综述表明,胰腺癌管理正朝着个性化、侵入性较小且更有效的方法发生范式转变。