Suppression of cancer proliferation and metastasis by a versatile nanomedicine integrating photodynamic therapy, photothermal therapy, and enzyme inhibition.


Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 09 2020
Historique:
received: 21 01 2020
revised: 10 06 2020
accepted: 11 06 2020
pubmed: 21 6 2020
medline: 15 5 2021
entrez: 21 6 2020
Statut: ppublish

Résumé

Cancer therapeutics are varied and target diverse processes in cancer progression. Photodynamic therapy (PDT), photothermal therapy (PTT), and the inhibition of pro-cancer proteases are non-invasive anticancer therapeutics that attract increasing attentions for their enhanced specificities and milder systemic toxicities compared to traditional therapeutics. These modalities offer advantages to compensate for the shortcomings of their counterparts. For instance, PDT or PTT efficiently eliminates locally confined tumor cells while exhibiting no effect on metastatic tumor cells. In contrast, the inhibition of pro-cancer proteases systemically suppresses the proliferation and metastasis of cancer cells but does not eradicate existing cancer cells. To synergize these therapeutics, we hereby report a versatile nanoparticle that integrates the effects of PDT, PTT, and enzyme-inhibition. This nanoparticle (CIKP-NP) was synthesized by covalently or non-covalently modifying a photothermal nanoparticle with a photosensitizer, a pro-cancer protease inhibitor, and an albumin-binding molecule. After confirming the PDT, PTT, albumin-binding, and enzyme-inhibition properties at the molecular level, we demonstrated that CIKP-NP killed tumor cells through PDT or PTT and suppressed tumor cell invasion through enzyme-inhibition. In addition, through a breast cancer xenograft mouse model, we demonstrated that CIKP-NP suppressed tumor growth by PDT or PTT effect. Notably, the synergism of PDT and PTT significantly enhanced its anticancer efficiency. Furthermore, CIKP-NP significantly suppressed cancer metastasis in a lung metastatic mouse model. Last, biodistribution and the in vivo retention of CIKP-NP confirmed the tumor-targeting property. Beyond demonstrating the anti-tumor and anti-metastatic efficacy of CIKP-NP, our study also suggests a new strategy to synergize multiple anticancer therapeutics.

Identifiants

pubmed: 32562802
pii: S1742-7061(20)30351-2
doi: 10.1016/j.actbio.2020.06.021
pii:
doi:

Substances chimiques

Photosensitizing Agents 0
Gold 7440-57-5

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

541-553

Informations de copyright

Copyright © 2020. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Dong Wang (D)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.

Wenzhen Liu (W)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.

Le Wang (L)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.

Yu Wang (Y)

College of Life Science, Fujian Agriculture and Forestry University, Fuzhou 350002, PR China.

Christopher Kai Liao (CK)

Institute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), 117608, Singapore.

Jincan Chen (J)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.

Ping Hu (P)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China; College of Chemistry, Fuzhou University, Fuzhou 350116, PR China.

Wanjin Hong (W)

Institute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), 117608, Singapore.

Mingdong Huang (M)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; College of Chemistry, Fuzhou University, Fuzhou 350116, PR China.

Zhuo Chen (Z)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China. Electronic address: zchen@fjirsm.ac.cn.

Peng Xu (P)

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fujian College, University of Chinese Academy of Sciences, Fujian 350002, PR China; College of Biological Science and Engineering, Fuzhou University, Fuzhou 350116, PR China; Institute of Molecular and Cell Biology, A*STAR (Agency for Science, Technology and Research), 117608, Singapore. Electronic address: xupeng@fjirsm.ac.cn.

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