Dai Hong, Chen Xingxuan, Yang Jiawen, Loiola Rodrigo Azevedo, Lu Aiping, Cheung Kenneth C P
Department of Chemistry, The Hong Kong University of Science and Technology, Kowloon, Hong Kong SAR, China.
Phenome Research Center, School of Chinese Medicine, Hong Kong Baptist University, Kowloon, Hong Kong SAR, China.
Front Cell Dev Biol. 2024 Dec 18;12:1460544. doi: 10.3389/fcell.2024.1460544. eCollection 2024.
Pancreatic cancer is one of the most lethal cancers, with a 5-year overall survival rate of less than 10%. Despite the development of novel therapies in recent decades, current chemotherapeutic strategies offer limited clinical benefits due to the high heterogeneity and desmoplastic tumor microenvironment (TME) of pancreatic cancer as well as inefficient drug penetration. Antibody- and nucleic acid-based targeting therapies have emerged as strong contenders in pancreatic cancer drug discovery. Numerous studies have shown that these strategies can significantly enhance drug accumulation in tumors while reducing systemic toxicity. Additionally, electron microscopy (EM) has been a critical tool for high-resolution analysis of the TME, providing insights into the ultrastructural changes associated with pancreatic cancer progression and treatment responses. This review traces the current and technological advances in EM, particularly the development of ultramicrotomy and improvements in sample preparation that have facilitated the detailed visualization of cellular and extracellular components of the TME. This review highlights the contribution of EM in assessing the efficacy of therapeutic agents, from revealing apoptotic changes to characterizing the effects of novel compounds like ionophore antibiotic gramicidin A on cellular ultrastructures. Moreover, the review delves into the potential of EM in studying the interactions between the tumor microbiome and cancer cell migration, as well as in aiding the development of targeted therapies like antibody-drug conjugates (ADCs) and aptamer-drug conjugates (ApDCs).
胰腺癌是最致命的癌症之一,其5年总生存率低于10%。尽管近几十年来有了新的治疗方法,但由于胰腺癌的高度异质性、促结缔组织增生性肿瘤微环境(TME)以及药物渗透效率低下,目前的化疗策略在临床上的益处有限。基于抗体和核酸的靶向治疗已成为胰腺癌药物研发中的有力竞争者。大量研究表明,这些策略可以显著提高药物在肿瘤中的蓄积,同时降低全身毒性。此外,电子显微镜(EM)一直是对TME进行高分辨率分析的关键工具,它能深入了解与胰腺癌进展和治疗反应相关的超微结构变化。本综述追溯了EM的当前进展和技术进步,特别是超薄切片技术的发展以及样品制备的改进,这些都有助于详细观察TME的细胞和细胞外成分。本综述强调了EM在评估治疗药物疗效方面的贡献,从揭示凋亡变化到表征离子载体抗生素短杆菌肽A等新型化合物对细胞超微结构的影响。此外,本综述还探讨了EM在研究肿瘤微生物群与癌细胞迁移之间的相互作用,以及在辅助抗体-药物偶联物(ADC)和适配体-药物偶联物(ApDC)等靶向治疗的开发方面的潜力。