Cu(ii)-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapyopen access
- Authors
- Jung, Hyo Sung; Koo, Seyoung; Won, Miae; An, Seeun; Park, Haebeen; Sessler, Jonathan L.; Han, Jiyou; Kim, Jong Seung
- Issue Date
- Feb-2023
- Publisher
- Royal Society of Chemistry
- Citation
- Chemical Science, v.14, no.7, pp 1808 - 1819
- Pages
- 12
- Indexed
- SCIE
SCOPUS
- Journal Title
- Chemical Science
- Volume
- 14
- Number
- 7
- Start Page
- 1808
- End Page
- 1819
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/118595
- DOI
- 10.1039/d2sc03945a
- ISSN
- 2041-6520
2041-6539
- Abstract
- Chemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficacy of these modalities against CSC remains limited. Here, we report a new generation photosensitizer, CA9-BPS-Cu(ii), a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting via carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of CA9-BPS-Cu(ii) was evident from the enhanced affinity of CA9-BPS-Cu(ii) towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed vs. CD133-negative cells. Moreover, the efficacy of CA9-BPS-Cu(ii) was successfully demonstrated in a xenograft mouse tumour model. © 2023 The Royal Society of Chemistry.
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