反义疗法的进展。

Hematologic pathology Pub Date : 1995-01-01
S T Crooke
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引用次数: 0

摘要

反义技术提供了创造足以支持高度同型选择性药理学的化合物的潜力(即,药理学试剂的特异性足以仅影响相关蛋白的多基因家族中的一种同型)。然而,人们对这项技术潜力的热情受到了对其兑现承诺能力的质疑。最根本的问题是:能不能制造出具有可接受的药物特性的寡核苷酸?这篇综述讨论了最近的进展,有助于确定磷硫寡核苷酸的药代动力学,药理学和毒理学性质。寡核苷酸在药物化学方面的进展导致了广泛的新化学类别。
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Progress in antisense therapeutics.

Antisense technology offers the potential to create compounds specific enough to support highly isotypically selective pharmacology (i.e., pharmacologic agents specific enough to affect only one isotype in a multigene family of related proteins). However, enthusiasm about the potential of the technology has been appropriately tempered by questions about its ability to deliver on its promise. The fundamental issue is: Can oligonucleotides that have acceptable drug properties be created? This review discusses recent progress that helps to define the pharmacokinetic, pharmacologic, and toxicologic properties of phosphorothioate oligonucleotides. Progress in the medicinal chemistry of oligonucleotides that has resulted in a wide range of new chemical classes is also described.

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Topobiology in hematopoiesis. Progress in antisense therapeutics. Ex vivo expansion of hematopoietic progenitor cells in human cord blood: an effect enhanced by cord blood serum. Lineage identification of acute leukemias: relevance of immunologic and ultrastructural techniques. Bone marrow morphology during induction phase of therapy for acute myeloid leukemia (AML).
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