An Indocyanine Green‐Based Nanoprobe for In Vivo Detection of Cellular Senescence
There is an urgent need to improve conventional cancer‐treatments by preventing detrimental side effects, cancer recurrence and metastases. Recent studies have shown that presence of senescent cells in tissues treated with chemo‐ or radiotherapy can be used to predict the effectiveness of cancer tre...
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Published in | Angewandte Chemie Vol. 136; no. 25 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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17.06.2024
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Abstract | There is an urgent need to improve conventional cancer‐treatments by preventing detrimental side effects, cancer recurrence and metastases. Recent studies have shown that presence of senescent cells in tissues treated with chemo‐ or radiotherapy can be used to predict the effectiveness of cancer treatment. However, although the accumulation of senescent cells is one of the hallmarks of cancer, surprisingly little progress has been made in development of strategies for their detection in vivo. To address a lack of detection tools, we developed a biocompatible, injectable organic nanoprobe (NanoJagg), which is selectively taken up by senescent cells and accumulates in the lysosomes. The NanoJagg probe is obtained by self‐assembly of indocyanine green (ICG) dimers using a scalable manufacturing process and characterized by a unique spectral signature suitable for both photoacoustic tomography (PAT) and fluorescence imaging. In vitro, ex vivo and in vivo studies all indicate that NanoJaggs are a clinically translatable probe for detection of senescence and their PAT signal makes them suitable for longitudinal monitoring of the senescence burden in solid tumors after chemotherapy or radiotherapy.
Sound of Senescence: A nanostructured organic probe, NanoJaggs, can be used as photoacoustic contrast agent for in vivo imaging of the senescent cell burden in post‐chemotherapy tumors. Made of indocyanine green (ICG) dimers, 30 nm nanoparticles exploit an active endocytosis mechanism and increase the number of lysosomes to specifically light up senescent cells implicated in cancer initiation and progression. |
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AbstractList | There is an urgent need to improve conventional cancer‐treatments by preventing detrimental side effects, cancer recurrence and metastases. Recent studies have shown that presence of senescent cells in tissues treated with chemo‐ or radiotherapy can be used to predict the effectiveness of cancer treatment. However, although the accumulation of senescent cells is one of the hallmarks of cancer, surprisingly little progress has been made in development of strategies for their detection in vivo. To address a lack of detection tools, we developed a biocompatible, injectable organic nanoprobe (NanoJagg), which is selectively taken up by senescent cells and accumulates in the lysosomes. The NanoJagg probe is obtained by self‐assembly of indocyanine green (ICG) dimers using a scalable manufacturing process and characterized by a unique spectral signature suitable for both photoacoustic tomography (PAT) and fluorescence imaging. In vitro, ex vivo and in vivo studies all indicate that NanoJaggs are a clinically translatable probe for detection of senescence and their PAT signal makes them suitable for longitudinal monitoring of the senescence burden in solid tumors after chemotherapy or radiotherapy. There is an urgent need to improve conventional cancer‐treatments by preventing detrimental side effects, cancer recurrence and metastases. Recent studies have shown that presence of senescent cells in tissues treated with chemo‐ or radiotherapy can be used to predict the effectiveness of cancer treatment. However, although the accumulation of senescent cells is one of the hallmarks of cancer, surprisingly little progress has been made in development of strategies for their detection in vivo. To address a lack of detection tools, we developed a biocompatible, injectable organic nanoprobe (NanoJagg), which is selectively taken up by senescent cells and accumulates in the lysosomes. The NanoJagg probe is obtained by self‐assembly of indocyanine green (ICG) dimers using a scalable manufacturing process and characterized by a unique spectral signature suitable for both photoacoustic tomography (PAT) and fluorescence imaging. In vitro, ex vivo and in vivo studies all indicate that NanoJaggs are a clinically translatable probe for detection of senescence and their PAT signal makes them suitable for longitudinal monitoring of the senescence burden in solid tumors after chemotherapy or radiotherapy. Sound of Senescence: A nanostructured organic probe, NanoJaggs, can be used as photoacoustic contrast agent for in vivo imaging of the senescent cell burden in post‐chemotherapy tumors. Made of indocyanine green (ICG) dimers, 30 nm nanoparticles exploit an active endocytosis mechanism and increase the number of lysosomes to specifically light up senescent cells implicated in cancer initiation and progression. |
Author | Hartono, Muhamad Ge, Jianfeng Macias, David Bohndiek, Sarah E. González‐Gualda, Estela Vernet, Aude Denholm, Mary Muñoz‐Espín, Daniel Popov, Andrea Bistrović Golinska, Monika Ou, Hui‐Ling Fruk, Ljiljana Brown, Emma L. Joseph, James Baker, Andrew G. Else, Thomas R. Sanghera, Chandan Greer, Heather F. Morsli, Samir |
Author_xml | – sequence: 1 givenname: Andrew G. surname: Baker fullname: Baker, Andrew G. organization: University of Cambridge – sequence: 2 givenname: Muhamad surname: Hartono fullname: Hartono, Muhamad organization: University of Cambridge – sequence: 3 givenname: Hui‐Ling surname: Ou fullname: Ou, Hui‐Ling organization: University of Cambridge – sequence: 4 givenname: Andrea Bistrović surname: Popov fullname: Popov, Andrea Bistrović organization: University of Cambridge – sequence: 5 givenname: Emma L. surname: Brown fullname: Brown, Emma L. organization: Cancer Research UK Cambridge Institute – sequence: 6 givenname: James surname: Joseph fullname: Joseph, James organization: University of Dundee – sequence: 7 givenname: Monika surname: Golinska fullname: Golinska, Monika organization: Cancer Research UK Cambridge Institute – sequence: 8 givenname: Estela surname: González‐Gualda fullname: González‐Gualda, Estela organization: University of Cambridge – sequence: 9 givenname: David surname: Macias fullname: Macias, David organization: Universidad de Sevilla – sequence: 10 givenname: Jianfeng surname: Ge fullname: Ge, Jianfeng organization: University of Cambridge – sequence: 11 givenname: Mary surname: Denholm fullname: Denholm, Mary organization: University of Cambridge – sequence: 12 givenname: Samir surname: Morsli fullname: Morsli, Samir organization: University of Cambridge – sequence: 13 givenname: Chandan surname: Sanghera fullname: Sanghera, Chandan organization: University of Cambridge – sequence: 14 givenname: Thomas R. surname: Else fullname: Else, Thomas R. organization: Cancer Research UK Cambridge Institute – sequence: 15 givenname: Heather F. surname: Greer fullname: Greer, Heather F. organization: University of Cambridge – sequence: 16 givenname: Aude surname: Vernet fullname: Vernet, Aude organization: Cancer Research UK Cambridge Institute – sequence: 17 givenname: Sarah E. surname: Bohndiek fullname: Bohndiek, Sarah E. organization: Cancer Research UK Cambridge Institute – sequence: 18 givenname: Daniel surname: Muñoz‐Espín fullname: Muñoz‐Espín, Daniel email: dm742@cam.ac.uk organization: University of Cambridge – sequence: 19 givenname: Ljiljana orcidid: 0000-0003-2104-5817 surname: Fruk fullname: Fruk, Ljiljana email: lf389@cam.ac.uk organization: University of Cambridge |
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SubjectTerms | Biocompatibility Cancer Cancer therapies Cellular senescence Chemotherapy Development strategies endocytosis ICG nanoprobe In vivo methods and tests Lysosomes Manufacturing industry Metastases Photoacoustic effect photoacoustic tomography (PAT) Radiation therapy Self-assembly Senescence Side effects Solid tumors Spectral signatures |
Title | An Indocyanine Green‐Based Nanoprobe for In Vivo Detection of Cellular Senescence |
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