Suppr超能文献

针对 Hippo 信号通路的新型治疗方法。

New Therapeutic Approach for Targeting Hippo Signalling Pathway.

机构信息

PEP Therapy, 45 rue du Cardinal Lemoine, 75005, Paris, France.

CIMI Paris, Inserm U1135, 91, bd de l'hôpital, 75013, Paris, France.

出版信息

Sci Rep. 2019 Mar 18;9(1):4771. doi: 10.1038/s41598-019-41404-w.

Abstract

Nuclear localization signals are short amino acid sequences that target proteins for nuclear import. In this manuscript, we have generated a chimeric tri-functional peptide composed of a cell penetrating peptide (CPP), a nuclear localization sequence and an interfering peptide blocking the interaction between TEAD and YAP, two transcription factors involved in the Hippo signalling pathway, whose deregulation is related to several types of cancer. We have validated the cell penetration and nuclear localization by flow cytometry and fluorescence microscopy and shown that the new generated peptide displays an apoptotic effect in tumor cell lines thanks to the specific nuclear delivery of the cargo, which targets a protein/protein interaction in the nucleus. In addition, the peptide has an anti-tumoral effect in vivo in xenograft models of breast cancer. The chimeric peptide designed in the current study shows encouraging prospects for developing nuclear anti- neoplastic drugs.

摘要

核定位信号是短的氨基酸序列,可将蛋白质靶向入核。在本研究中,我们构建了一个由细胞穿透肽(CPP)、核定位序列和干扰肽组成的嵌合三功能肽,干扰肽可阻断转录因子 TEAD 和 YAP 之间的相互作用,这两个转录因子参与 Hippo 信号通路,其失调与多种类型的癌症相关。我们通过流式细胞术和荧光显微镜验证了细胞穿透和核定位,表明新生成的肽由于货物的特异性核递送而在肿瘤细胞系中显示出凋亡作用,货物靶向核内的蛋白质/蛋白质相互作用。此外,该肽在乳腺癌的异种移植模型中具有体内抗肿瘤作用。本研究设计的嵌合肽为开发核抗肿瘤药物展示出了令人鼓舞的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbdc/6423280/8fe4e51c0ddd/41598_2019_41404_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验