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核酸适配体临床开发的新见解。

New insight into clinical development of nucleic acid aptamers.

作者信息

Esposito Carla Lucia, Catuogno Silvia, de Franciscis Vittorio, Cerchia Laura

机构信息

Istituto di Endocrinologia e Oncologia Sperimentale, CNR, Naples, Italy.

出版信息

Discov Med. 2011 Jun;11(61):487-96.

Abstract

Nucleic acid-based aptamers have been shown as high-affinity ligands and potential antagonists of disease-associated proteins. Aptamers, isolated from combinatorial libraries by an iterative in vitro selection process, discriminate between closely related targets and are characterized by high specificity and low toxicity thus representing a valid alternative to antibodies to target specific proteins of biomedical interest. Moreover, they are non-immunogenic and can be easily stabilized by chemical modifications thus expanding their therapeutic potential. Here, we will focus on the structural and functional features of aptamers that have entered the clinical development pipeline together with those aptamers holding great potential as therapeutics in preclinical studies. The future perspectives of aptamers as therapeutics will be discussed as well.

摘要

基于核酸的适配体已被证明是疾病相关蛋白的高亲和力配体和潜在拮抗剂。通过迭代体外筛选过程从组合文库中分离出的适配体,能够区分密切相关的靶标,具有高特异性和低毒性的特点,因此是针对具有生物医学意义的特定蛋白的抗体的有效替代品。此外,它们无免疫原性,可通过化学修饰轻松稳定,从而扩展了其治疗潜力。在此,我们将重点关注已进入临床开发阶段的适配体的结构和功能特征,以及那些在临床前研究中具有巨大治疗潜力的适配体。还将讨论适配体作为治疗剂的未来前景。

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