Zhang Hui, Wang Zhibo, Xie Lin, Zhang Yibin, Deng Tanggang, Li Jianglin, Liu Jing, Xiong Wei, Zhang Lei, Zhang Lin, Peng Bo, He Leye, Ye Mao, Hu Xiaoxiao, Tan Weihong
Molecular Science and Biomedicine Laboratory, State Key Laboratory for Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Collaborative Innovation Center for Molecular Engineering for Theranostics, Hunan University, Changsha 410082, China.
Molecular Biology Research Center, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
Mol Ther Nucleic Acids. 2018 Sep 7;12:758-768. doi: 10.1016/j.omtn.2018.07.015. Epub 2018 Aug 4.
Renal cell carcinoma (RCC) is the most common malignant tumor of the urinary system, and it has a high frequency of local invasion and distant metastasis. Although multiple advances have been made in the diagnosis and therapy of RCC, the vast majority of patients with metastatic RCC remain incurable. In this study, an aptamer named SW-4 against RCC 786-O cells was identified from a known sequence pool. The identified aptamer exhibited high binding affinity for target cells with dissociation constants in the nanomolar range. Binding analysis revealed that SW-4 only bound to RCC 786-O cells, but not HEK293T cells or human proximal tubular HK-2 cells, indicating that SW-4 has excellent binding selectivity. By sequence optimization, the 26-nt truncated SW-4b demonstrated improved binding affinity, and it was internalized into target cells via caveolae-mediated endocytosis in a temperature-dependent manner. Furthermore, fluorescence imaging confirmed that SW-4b accumulated at tumor sites in 786-O xenograft nude mice models and specifically recognized clinical RCC tissues. Meanwhile, SW-4b inhibited proliferation of 786-O cells by arresting cell cycle progression at the S phase. Taken together, these results indicate that SW-4b is a potential candidate for development into a novel tool for diagnosis and targeted therapy of RCC.
肾细胞癌(RCC)是泌尿系统最常见的恶性肿瘤,具有较高的局部侵袭和远处转移发生率。尽管在RCC的诊断和治疗方面已经取得了多项进展,但绝大多数转移性RCC患者仍然无法治愈。在本研究中,从已知序列库中筛选出一种针对RCC 786 - O细胞的适体SW - 4。所鉴定的适体对靶细胞表现出高结合亲和力,解离常数在纳摩尔范围内。结合分析表明,SW - 4仅与RCC 786 - O细胞结合,而不与HEK293T细胞或人近端肾小管HK - 2细胞结合,这表明SW - 4具有优异的结合选择性。通过序列优化,26个核苷酸截短的SW - 4b表现出更高的结合亲和力,并且它以温度依赖的方式通过小窝介导的内吞作用内化到靶细胞中。此外,荧光成像证实SW - 4b在786 - O异种移植裸鼠模型的肿瘤部位积聚,并特异性识别临床RCC组织。同时,SW - 4b通过使细胞周期进程停滞在S期来抑制786 - O细胞的增殖。综上所述,这些结果表明SW - 4b是开发成为RCC诊断和靶向治疗新工具的潜在候选物。