New Therapeutic Approach for Targeting Hippo Signalling Pathway

被引:20
|
作者
Dominguez-Berrocal, Leticia [1 ]
Cirri, Erica [1 ]
Zhang, Xiguang [2 ]
Andrini, Laura [3 ]
Marin, Gustavo H. [3 ]
Lebel-Binay, Sophie [1 ]
Rebollo, Angelita [2 ]
机构
[1] PEP Therapy, 45 Rue Cardinal Lemoine, F-75005 Paris, France
[2] CIMI Paris, Inserm U1135, 91 Bd Hop, F-75013 Paris, France
[3] UNLP, CONICET, Fac Ciencias Med, 60 & 120 Code, RA-1900 La Plata, Buenos Aires, Argentina
关键词
NUCLEAR-LOCALIZATION SIGNALS; CELL-PENETRATING PEPTIDES; YES-ASSOCIATED PROTEIN; ORGAN SIZE CONTROL; TEAD-YAP COMPLEX; EMERGING ROLE; RECOGNITION; NUCLEOPLASMIN; TRANSPORT; IMPORT;
D O I
10.1038/s41598-019-41404-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
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页数:11
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