Red light‐activated depletion of drug‐refractory glioblastoma stem cells and chemosensitization of an acquired‐resistant mesenchymal phenotype.
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| Title: | Red light‐activated depletion of drug‐refractory glioblastoma stem cells and chemosensitization of an acquired‐resistant mesenchymal phenotype. |
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| Authors: | Spring, Bryan Q.1,2 (AUTHOR), Watanabe, Kohei1,3 (AUTHOR), Ichikawa, Megumi1 (AUTHOR), Mallidi, Srivalleesha1,4 (AUTHOR), Matsudaira, Tatsuyuki1 (AUTHOR), Timerman, Dmitriy1 (AUTHOR), Swain, Joseph W. R.1 (AUTHOR), Mai, Zhiming1 (AUTHOR), Wakimoto, Hiroaki5 (AUTHOR), Hasan, Tayyaba1,6 (AUTHOR) thasan@mgh.harvard.edu |
| Source: | Photochemistry & Photobiology. Jan2025, Vol. 101 Issue 1, p215-229. 15p. |
| Subjects: | Red light, Cancer stem cells, Surgical margin, Stem cells, Temozolomide |
| Abstract: | Glioblastoma stem cells (GSCs) are potent tumor initiators resistant to radiochemotherapy, and this subpopulation is hypothesized to re‐populate the tumor milieu due to selection following conventional therapies. Here, we show that 5‐aminolevulinic acid (ALA) treatment—a pro‐fluorophore used for fluorescence‐guided cancer surgery—leads to elevated levels of fluorophore conversion in patient‐derived GSC cultures, and subsequent red light‐activation induces apoptosis in both intrinsically temozolomide chemotherapy‐sensitive and ‐resistant GSC phenotypes. Red light irradiation of ALA‐treated cultures also exhibits the ability to target mesenchymal GSCs (Mes–GSCs) with induced temozolomide resistance. Furthermore, sub‐lethal light doses restore Mes–GSC sensitivity to temozolomide, abrogating GSC‐acquired chemoresistance. These results suggest that ALA is not only useful for fluorescence‐guided glioblastoma tumor resection, but that it also facilitates a GSC drug‐resistance agnostic, red light‐activated modality to mop up the surgical margins and prime subsequent chemotherapy. [ABSTRACT FROM AUTHOR] |
| Copyright of Photochemistry & Photobiology is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 183913218 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Red light‐activated depletion of drug‐refractory glioblastoma stem cells and chemosensitization of an acquired‐resistant mesenchymal phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Spring%2C+Bryan+Q%2E%22">Spring, Bryan Q.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Watanabe%2C+Kohei%22">Watanabe, Kohei</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ichikawa%2C+Megumi%22">Ichikawa, Megumi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mallidi%2C+Srivalleesha%22">Mallidi, Srivalleesha</searchLink><relatesTo>1,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Matsudaira%2C+Tatsuyuki%22">Matsudaira, Tatsuyuki</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Timerman%2C+Dmitriy%22">Timerman, Dmitriy</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Swain%2C+Joseph+W%2E+R%2E%22">Swain, Joseph W. R.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mai%2C+Zhiming%22">Mai, Zhiming</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wakimoto%2C+Hiroaki%22">Wakimoto, Hiroaki</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hasan%2C+Tayyaba%22">Hasan, Tayyaba</searchLink><relatesTo>1,6</relatesTo> (AUTHOR)<i> thasan@mgh.harvard.edu</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Photochemistry+%26+Photobiology%22">Photochemistry & Photobiology</searchLink>. Jan2025, Vol. 101 Issue 1, p215-229. 15p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Red+light%22">Red light</searchLink><br /><searchLink fieldCode="DE" term="%22Cancer+stem+cells%22">Cancer stem cells</searchLink><br /><searchLink fieldCode="DE" term="%22Surgical+margin%22">Surgical margin</searchLink><br /><searchLink fieldCode="DE" term="%22Stem+cells%22">Stem cells</searchLink><br /><searchLink fieldCode="DE" term="%22Temozolomide%22">Temozolomide</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Glioblastoma stem cells (GSCs) are potent tumor initiators resistant to radiochemotherapy, and this subpopulation is hypothesized to re‐populate the tumor milieu due to selection following conventional therapies. Here, we show that 5‐aminolevulinic acid (ALA) treatment—a pro‐fluorophore used for fluorescence‐guided cancer surgery—leads to elevated levels of fluorophore conversion in patient‐derived GSC cultures, and subsequent red light‐activation induces apoptosis in both intrinsically temozolomide chemotherapy‐sensitive and ‐resistant GSC phenotypes. Red light irradiation of ALA‐treated cultures also exhibits the ability to target mesenchymal GSCs (Mes–GSCs) with induced temozolomide resistance. Furthermore, sub‐lethal light doses restore Mes–GSC sensitivity to temozolomide, abrogating GSC‐acquired chemoresistance. These results suggest that ALA is not only useful for fluorescence‐guided glioblastoma tumor resection, but that it also facilitates a GSC drug‐resistance agnostic, red light‐activated modality to mop up the surgical margins and prime subsequent chemotherapy. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Photochemistry & Photobiology is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/php.13985 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 215 Subjects: – SubjectFull: Red light Type: general – SubjectFull: Cancer stem cells Type: general – SubjectFull: Surgical margin Type: general – SubjectFull: Stem cells Type: general – SubjectFull: Temozolomide Type: general Titles: – TitleFull: Red light‐activated depletion of drug‐refractory glioblastoma stem cells and chemosensitization of an acquired‐resistant mesenchymal phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Spring, Bryan Q. – PersonEntity: Name: NameFull: Watanabe, Kohei – PersonEntity: Name: NameFull: Ichikawa, Megumi – PersonEntity: Name: NameFull: Mallidi, Srivalleesha – PersonEntity: Name: NameFull: Matsudaira, Tatsuyuki – PersonEntity: Name: NameFull: Timerman, Dmitriy – PersonEntity: Name: NameFull: Swain, Joseph W. R. – PersonEntity: Name: NameFull: Mai, Zhiming – PersonEntity: Name: NameFull: Wakimoto, Hiroaki – PersonEntity: Name: NameFull: Hasan, Tayyaba IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 00318655 Numbering: – Type: volume Value: 101 – Type: issue Value: 1 Titles: – TitleFull: Photochemistry & Photobiology Type: main |
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