A NanoFlare‐Based Strategy for In Situ Tumor Margin Demarcation and Neoadjuvant Gene/Photothermal Therapy. Issue 50 (7th October 2018)
- Record Type:
- Journal Article
- Title:
- A NanoFlare‐Based Strategy for In Situ Tumor Margin Demarcation and Neoadjuvant Gene/Photothermal Therapy. Issue 50 (7th October 2018)
- Main Title:
- A NanoFlare‐Based Strategy for In Situ Tumor Margin Demarcation and Neoadjuvant Gene/Photothermal Therapy
- Authors:
- Yan, Rong
Chen, Jie
Wang, Jianhao
Rao, Jiaming
Du, Xuancheng
Liu, Yongming
Zhang, Leshuai
Qiu, Lin
Liu, Bo
Zhao, Yuan‐Di
Jiang, Pengju
Chen, Chunying
Li, Yong‐Qiang - Abstract:
- Abstract: Accurate tumor margin demarcation in situ remains a paramount challenge. Herein, a NanoFlare (also known as spherical‐nucleic‐acid technology) based strategy is reported for in situ tumor margin delineation by transforming and amplifying the pathophysiological redox signals of tumor microenvironment. The NanoFlare designed (named AuNS‐ASON) is based on gold nanostar (AuNS) coated with a dense shell of disulfide bridge‐inserted and cyanine dyes‐labeled antisense oligonucleotides (ASON) targeting survivin mRNA. The unique anisotropic ASON‐spike nanostructure endows the AuNS‐ASON with universal cellular internalization of tumor cells, while the disulfide bridge inserted confers response specificity toward redox activation. In vitro experiments demonstrate that the AuNS‐ASON can discriminate tumor cells rapidly with activated fluorescence signals (>100‐fold) in 2 h, and further achieve synergistic gene/photothermal tumor cells ablation upon near‐infrared laser irradiation. Remarkably, in situ tumor margin delineation with high accuracy and outstanding spatial resolution (<100 µm) in mice bearing different tumors is obtained based on the AuNS‐ASON, providing intraoperative guidance for tumor resection. Moreover, the AuNS‐ASON can enable efficient neoadjuvant gene/photothermal therapy before surgery to reduce tumor extent and increase resectability. The concept of NanoFlare‐based microenvironment signal transformation and amplification could be used as a general strategyAbstract: Accurate tumor margin demarcation in situ remains a paramount challenge. Herein, a NanoFlare (also known as spherical‐nucleic‐acid technology) based strategy is reported for in situ tumor margin delineation by transforming and amplifying the pathophysiological redox signals of tumor microenvironment. The NanoFlare designed (named AuNS‐ASON) is based on gold nanostar (AuNS) coated with a dense shell of disulfide bridge‐inserted and cyanine dyes‐labeled antisense oligonucleotides (ASON) targeting survivin mRNA. The unique anisotropic ASON‐spike nanostructure endows the AuNS‐ASON with universal cellular internalization of tumor cells, while the disulfide bridge inserted confers response specificity toward redox activation. In vitro experiments demonstrate that the AuNS‐ASON can discriminate tumor cells rapidly with activated fluorescence signals (>100‐fold) in 2 h, and further achieve synergistic gene/photothermal tumor cells ablation upon near‐infrared laser irradiation. Remarkably, in situ tumor margin delineation with high accuracy and outstanding spatial resolution (<100 µm) in mice bearing different tumors is obtained based on the AuNS‐ASON, providing intraoperative guidance for tumor resection. Moreover, the AuNS‐ASON can enable efficient neoadjuvant gene/photothermal therapy before surgery to reduce tumor extent and increase resectability. The concept of NanoFlare‐based microenvironment signal transformation and amplification could be used as a general strategy to guide the design of activatable nanoprobes for cancer theranostics. Abstract : A NanoFlare‐based strategy for in situ tumor margin demarcation and neoadjuvant gene/photothemal therapy is reported. In virtue of anisotropic antisense oligonucleotides‐spike nanostructure, the NanoFlare can enter tumor cells universally regardless of cell types and produce redox‐activated fluorescence signals. The NanoFlare enables accurate intraoperative margin demarcation of differetn tumors and efficient gene/photothermal neoadjuvant therapy in vivo. … (more)
- Is Part Of:
- Small. Volume 14:Issue 50(2018)
- Journal:
- Small
- Issue:
- Volume 14:Issue 50(2018)
- Issue Display:
- Volume 14, Issue 50 (2018)
- Year:
- 2018
- Volume:
- 14
- Issue:
- 50
- Issue Sort Value:
- 2018-0014-0050-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2018-10-07
- Subjects:
- fluorescence turn‐on -- NanoFlare -- redox signals -- tumor margin demarcation -- tumor microenvironment
Nanotechnology -- Periodicals
Nanoparticles -- Periodicals
Microtechnology -- Periodicals
620.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1613-6829 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/smll.201802745 ↗
- Languages:
- English
- ISSNs:
- 1613-6810
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8309.952000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9128.xml