期刊文献+

核酸适体在儿童恶性肿瘤诊断与靶向治疗中的研究进展

Research advances in the role of aptamers in the diagnosis and targeted therapy of pediatric cancer
原文传递
导出
摘要 核酸适体(aptamer)是运用指数富集的配体系统进化技术(SELEX)从体外人工合成的随机寡核苷酸序列库中经过多轮筛选后得到的单链DNA或RNA,它可以高亲和力与金属离子、小分子、糖类、脂质以及蛋白质等靶标特异性结合,具有制备方便、热稳定性好、低免疫原性等优点。核酸适体在分子成像、生物传感、疾病早期诊断及药物靶向治疗等生物医学领域中有很大的应用潜能。在儿童恶性肿瘤中,核酸适体技术具有实现肿瘤的早期诊断以及靶向治疗的应用前景,可避免传统化疗带来的儿童生长发育障碍以及远期的脏器功能不良等副作用。本文总结了与儿童恶性肿瘤相关的核酸适体筛选与应用的研究进展。 Aptamers are single-stranded DNA or RNA which are isolated from synthesized random oligonucleotide library in vitro via systematic evolution of ligands by exponential enrichment(SELEX) and can bind to metal ions, small molecules, carbohydrates, lipids, proteins, and others targets with high affinity and specificity. Aptamers have the advantages of simple preparation, good thermal stability, and low immunogenicity and have great potential in the medical fields such as molecular imaging, biosensing, early diagnosis of diseases, and targeted therapy. Aptamer technology may be useful for early diagnosis and targeted therapy of pediatric cancer, and may avoid the side effects of conventional chemotherapy, such as growth and development disorders and long-term organ dysfunction. This article reviews the latest research advances in the selection and application of aptamers for pediatric cancer.
作者 张毅彬 王彦鹏 刘静 ZHANG lq-Bin;WANG Yan-Peng;LIU Jing.(Molecular Research Center, School of Life Sciences, Central South University, Changsha 410078, China)
出处 《中国当代儿科杂志》 CAS CSCD 北大核心 2018年第5期421-427,共7页 Chinese Journal of Contemporary Pediatrics
基金 国家自然科学基金(81470362) 中南大学研究生自主探索创新项目基金(2017zzts356 2017zzts355)
关键词 核酸适体 恶性肿瘤 诊断 靶向治疗 儿童 Aptamer Cancer Diagnosis Targeted therapy Child
  • 相关文献

参考文献3

二级参考文献49

  • 1武开宏,刘迎龙.小儿心脏肿瘤的诊断与治疗[J].中华小儿外科杂志,2006,27(12):659-660. 被引量:5
  • 2Maher EA, Furnari FB, Bachoo RM, Rowitch DH, Louis DN, Cavenee WK, et al. Malignant glioma: genetics and biologY of a grave matter. Genes Dev 2001; 15: 1311-33. 被引量:1
  • 3Okamoto I, Kenyon LC, Emlet DR, Mori T, Sasaki J, Hirosako S, et al. Expression of constitutively activated EGFRvlII in non-small cell lung cancer. Cancer Sci 2003; 94: 50-6. 被引量:1
  • 4Moscatello DK, Holgado-Madruga M, Godwin AK, Ramirez G, Gunn G, Zoltick PW, et al. Frequent expression of a mutant epidermal growth factor receptor in multiple human tumors. Cancer Res 1995; 55: 5536-9. 被引量:1
  • 5Kuan CT, Wikstrand C J, Bigner DD. EGF mutant receptor viii as a molecular target in cancer therapy. Endocr Relat Cancer 2001; 8: 83-96. 被引量:1
  • 6Furnari FB, Fenton T, Bachoo RM, Mukasa A, Stommel JM, Stegh A, et al. Malignant astrocytic glioma: genetics, biology, and paths to treatment. Genes Dev 2007; 21: 2683-710. 被引量:1
  • 7Cai XM, Tao BB, Wang LY, Liang YL, Jin JW, Yang Y, et al. Proteinphosphatase activity of PTEN inhibited the invasion of glioma cells with epidermal growth factor receptor mutation type III expression. Int J Cancer 2005; 117: 905-12. 被引量:1
  • 8Pelloski CE, Ballman KV, Furth AF, Zhang L, Lin E, Sulman EP, et al. Epidermal growth factor receptor variant III status defines clinically distinct subtypes of glioblastoma. J Clin Onco12007; 25: 2288-94. 被引量:1
  • 9Yoshimoto K, Dang J, Zhu S, Nathanson D, Huang 1-, Dumont R, et al. Development of a real-time RT-PCR assay for detecting EGFRvlII in glioblastoma samples. Clin Cancer Res 2008; 14: 488-93. 被引量:1
  • 10Reist C J, Archer GE, Kurpad SN, Wikstrand C J, Vaidyanathan G, Willingham MC, et al. Tumor-specific anti-epidermal growth factor receptor variant III monoclonal antibodies: use of the tyramine- cellobiose radioiodination method enhances cellular retention and uptake in tumor xenografts. Cancer Res 1995; 55: 4375-82. 被引量:1

共引文献66

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部