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一种抑制癌细胞中成纤维细胞生长因子受体异常信号传导的DNA适配体。

A DNA Aptamer That Inhibits the Aberrant Signaling of Fibroblast Growth Factor Receptor in Cancer Cells.

作者信息

Eguchi Akihiro, Ueki Ayaka, Hoshiyama Junya, Kuwata Keiko, Chikaoka Yoko, Kawamura Takeshi, Nagatoishi Satoru, Tsumoto Kouhei, Ueki Ryosuke, Sando Shinsuke

机构信息

Department of Chemistry and Biotechnology andDepartment of Bioengineering, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan.

Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8601, Japan.

出版信息

JACS Au. 2021 Apr 8;1(5):578-585. doi: 10.1021/jacsau.0c00121. eCollection 2021 May 24.

Abstract

Growth factor receptors are activated through dimerization by the binding of their ligands and play pivotal roles in normal cell function. However, the aberrant activity of the receptors has been associated with cancer malignancy. One of the main causes of the aberrant receptor activation is the overexpression of receptors and the resultant formation of unliganded receptor dimers, which can be activated in the absence of external ligand molecules. Thus, the unliganded receptor dimer is a promising target to inhibit aberrant signaling in cancer. Here, we report an aptamer that specifically binds to fibroblast growth factor receptor 2b and inhibits the aberrant receptor activation and signaling. Our investigation suggests that this aptamer inhibits the formation of the receptor dimer occurring in the absence of external ligand molecules. This work presents a new inhibitory function of aptamers and the possibility of oligonucleotide-based therapeutics for cancer.

摘要

生长因子受体通过其配体的结合而二聚化被激活,并在正常细胞功能中发挥关键作用。然而,受体的异常活性与癌症恶性肿瘤相关。受体异常激活的主要原因之一是受体的过度表达以及由此产生的无配体受体二聚体的形成,这些二聚体在没有外部配体分子的情况下也能被激活。因此,无配体受体二聚体是抑制癌症中异常信号传导的一个有前景的靶点。在此,我们报道了一种适体,它特异性结合成纤维细胞生长因子受体2b并抑制受体的异常激活和信号传导。我们的研究表明,这种适体抑制在没有外部配体分子时发生的受体二聚体的形成。这项工作展示了适体的一种新的抑制功能以及基于寡核苷酸的癌症治疗的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fab0/8395645/c011fb19db45/au0c00121_0001.jpg

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