Vandghanooni Somayeh, Eskandani Morteza, Barar Jaleh, Omidi Yadollah
Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Pharmaceutics, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Bioimpacts. 2019;9(2):67-70. doi: 10.15171/bi.2019.09. Epub 2018 Nov 30.
Aptamers ( Aps ) are short single-strand nucleic acids exhibiting unique 3D structure which facilitate their targeting potential against various cancer molecular markers ( CMMs ). Such features of Aps not only make them as suitable homing agents in targeted drug delivery systems (DDSs) but also candidate them as macromolecules that inhibit the interaction of the target ligand with other proteins. On the other hand, the conjugation of Aps with another therapeutic molecule such as antisense oligonucleotides (ASOs), siRNAs/miRNAs, Aps , toxins, chemotherapeutic agents, DNAzymes/Ribozymes provides hopeful strategy to eradicate the malignancies and overcome the off-target unwanted side effects. Such prominent features of Aps make them a promising treatment modality to overcome the tumor complexity and heterogeneity, which can be consequently applied for personalized therapy of cancer by using bispecific Ap-based therapeutics.
适配体(Aps)是短单链核酸,具有独特的三维结构,有利于其针对各种癌症分子标志物(CMMs)的靶向潜力。Aps的这些特性不仅使其成为靶向药物递送系统(DDSs)中合适的归巢剂,还使其成为抑制靶配体与其他蛋白质相互作用的大分子候选物。另一方面,Aps与另一种治疗分子如反义寡核苷酸(ASOs)、siRNAs/miRNAs、Aps、毒素、化疗药物、DNA酶/核酶的缀合提供了消除恶性肿瘤和克服脱靶不良副作用的有希望的策略。Aps的这些突出特性使其成为克服肿瘤复杂性和异质性的有前途的治疗方式,因此可以通过使用双特异性基于Ap的疗法应用于癌症的个性化治疗。