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诱饵寡脱氧核苷酸技术:乳腺癌治疗的新兴范例。

Decoy oligodeoxynucleotide technology: an emerging paradigm for breast cancer treatment.

机构信息

Department of Medical Biotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Bioinformatics Research Group, Mashhad University of Medical Sciences, Mashhad, Iran.

出版信息

Drug Discov Today. 2020 Jan;25(1):195-200. doi: 10.1016/j.drudis.2019.10.008. Epub 2019 Oct 25.

Abstract

Breast cancer is the most common cancer in women worldwide. Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer, which is resistant to conventional therapies. Therefore, there is an urgent need to identify new therapies for treating incurable breast cancer in patients. Decoy oligodeoxynucleotides (ODNs) are synthetic oligonucleotides that have a high affinity for a specific transcription factor and can be transfected into target cells to bind to their respective target and alter gene transcription. With these powerful tools available, it is highly possible to effectively regulate the expression of genes that are involved in the pathogenesis of breast cancer. Here, we highlight the studies using decoy ODNs for the development of novel therapies against breast cancer.

摘要

乳腺癌是全球女性最常见的癌症。三阴性乳腺癌(TNBC)是一种侵袭性乳腺癌亚型,对常规疗法具有抗性。因此,迫切需要为无法治愈的乳腺癌患者寻找新的治疗方法。诱饵寡脱氧核苷酸(ODN)是一种与特定转录因子具有高亲和力的合成寡核苷酸,可转染入靶细胞与各自的靶标结合,改变基因转录。有了这些强大的工具,就有可能有效地调节参与乳腺癌发病机制的基因的表达。在这里,我们重点介绍了使用诱饵 ODN 开发针对乳腺癌的新型治疗方法的研究。

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