AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
Article Link
Collect
Submit Manuscript
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Research Article

NVP-BEZ235/Chlorin-e6 co-loaded nanoparticles ablate breast cancer by biochemical and photodynamic synergistic effects

Ahmed Shaker Eltahan1,2,§Lu Liu1,2,4,§Chukwunweike Ikechukwu Okeke1,2Min Huang5Lu Han5Jing Chen1Xue Xue3( )Massimo Bottini1,4Weisheng Guo1( )Xing-Jie Liang1,2 ( )
CAS Key Laboratory for Biomedical Effects of Nanomaterials and NanosafetyCAS Center for Excellence in NanoscienceNationalCenter for Nanoscience and Technology of ChinaBeijing100190China
University of Chinese Academy of SciencesBeijing100049China
State Key Laboratory of Medicinal Chemical BiologyCollege of PharmacyNankai UniversityTianjin300350China
Department of Experimental Medicine and SurgeryUniversity of Rome Tor VergataRome00133Italy
Beijing Engineering Research Center of Printed ElectronicsBeijing Institute of Graphic CommunicationBeijing102600China

§ Ahmed Shaker Eltahan and Lu Liu contributed equally to this work.

Show Author Information

Abstract

Seeking profitable therapies for triple-negative breast cancer (TNBC) has attracted intense research interest. However, an efficient cure for TNBC remains an unresolved challenge in oncology. Herein, for the first time, we describe the use of polymeric nanoparticles loaded with NVP-BEZ235 and Chlorin-e6, denoted as NVP/Ce6@NPs, to overcome the adaptive treatment tolerance of TNBC by taking advantage of the synergistic effect between biochemical and photodynamic therapies. Upon laser irradiation, the NVP/Ce6@NPs generated reactive oxygen species (ROS) and efficiently induced the apoptosis of tumor cells through DNA damage. Furthermore, the released NVP-BEZ235 could prevent Chk1 phosphorylation-induced DNA damage repair, thus enhancing the sensitivity of tumor cells to ROS. Animal studies on mice bearing an MDA- MB-231 tumor validated that the NVP/Ce6@NPs had a greater therapeutic efficacy compared to that of monotherapies, with an inhibition ratio of 89.3%. Western blotting and cell viability analyses confirmed the inhibition of both MDA-MB-231 cell proliferation and Chk1 phosphorylation by NVP/Ce6@NPs. These findings provide a rational understanding of the synergistic effect of the biochemical/photodynamic therapy and pave the way for the development of efficient therapeutic approaches to fight against TNBC.

Graphical Abstract

Electronic Supplementary Material

Download File(s)
12274_2018_2074_MOESM1_ESM.pdf (1.4 MB)

References

【1】
【1】
 
 
Nano Research
Pages 4846-4858

{{item.num}}

Comments on this article

Go to comment

< Back to all reports

Review Status: {{reviewData.commendedNum}} Commended , {{reviewData.revisionRequiredNum}} Revision Required , {{reviewData.notCommendedNum}} Not Commended Under Peer Review

Review Comment

Close
Close
Cite this article:
Eltahan AS, Liu L, Okeke CI, et al. NVP-BEZ235/Chlorin-e6 co-loaded nanoparticles ablate breast cancer by biochemical and photodynamic synergistic effects. Nano Research, 2018, 11(9): 4846-4858. https://doi.org/10.1007/s12274-018-2074-0

1144

Views

7

Crossref

N/A

Web of Science

7

Scopus

0

CSCD

Received: 31 January 2018
Revised: 12 April 2018
Accepted: 13 April 2018
Published: 11 May 2018
© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2018