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反义脱氧核糖核酸作为癌症的靶向治疗药物:不再是梦想。

Antisense DNAs as targeted therapeutics for cancer: no longer a dream.

作者信息

Cho-Chung Yoon S

机构信息

Cellular Biochemistry Section, BRL, CCR, National Cancer Institute, NIH, Bethesda, MD 20892-1750, USA.

出版信息

Curr Opin Investig Drugs. 2002 Jun;3(6):934-9.

Abstract

Progress in antisense technology has been rapid, and the traditional antisense inhibition of gene expression has now been viewed at a genomic scale. This global view has led to a deeper understanding of the mechanism of action, the elimination of non-specific and undesirable side effects and, ultimately, greater efficacy and reduced toxicity for nucleic acid medicines. Several antisense oligonucleotides are in clinical trials; these are well tolerated and have therapeutic potential. Antisense oligonucleotides are promising molecular medicines with potential to treat human cancer in the foreseeable future.

摘要

反义技术进展迅速,传统的基因表达反义抑制现已在基因组规模上得到审视。这种全局观使得对作用机制有了更深入的理解,消除了非特异性和不良副作用,最终提高了核酸药物的疗效并降低了毒性。几种反义寡核苷酸正处于临床试验阶段;它们耐受性良好且具有治疗潜力。反义寡核苷酸是很有前景的分子药物,在可预见的未来有治疗人类癌症的潜力。

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