利用SELEX和抗基因方法靶向癌症治疗的DNA相关过程-当选择符合理性设计时

P. Majumder, M. Faria, H. Ulrich
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引用次数: 1

摘要

在我们全球称为癌症的多原因多步骤疾病中,通常相同或冗余的生化回路被各种突变事件的累积作用破坏或解耦。抗癌药物已经被广泛设计和选择,因为它们能够通过靶向蛋白质、mrna或DNA序列来特异性地与恶性细胞相互作用,这些蛋白质、mrna或DNA序列参与了转化表型的产生。在后基因组时代,有关DNA的可用信息的数量增加了基因组和相关蛋白质作为药物靶点的兴趣。SELEX (Systematic Evolution of L igands by EX ponential enrichment)技术和Anti-gene策略都是基于产生针对蛋白质或核酸对应物的高亲和力配体。SELEX和抗基因方法的不同理性背景可能是它们在抗癌治疗中互补作用的基础。关键词:适体,SELEX,抗基因,三联体形成分子,癌症,表观基因组靶向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting DNA Associated Processes for Cancer Therapy by the Use of SELEX and Anti-gene Approaches - When Selection Meets Rational Design
In the multi-cause and multi-step diseases we globally refer to as cancer, often the same or redundant bio- chemical circuits are disrupted or uncoupled by the cumulative action of diverse mutation events. Anticancer agents have been extensively designed and selected by their ability to specifically interact with malignant cells by the targeting of proteins, mRNAs or DNA sequences involved in the production of a transformed phenotype. In the post-genomic age, the amount of available information concerning DNA increases the interest of the genome and associated proteins as drug tar- gets. The SELEX (Systematic Evolution of L igands by EX ponential enrichment) technique and Anti-gene strategy are both based on the production of high affinity ligands targeted to protein or nucleic acid counterparts, respectively. The dif- ferent rational backgrounds of SELEX and Anti-gene approaches might be the basis for a complementary action in anti- cancer therapy. Keyword: Aptamer, SELEX, anti-gene, triplex-forming molecules, cancer, epigenome targeting.
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