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dc.contributor.authorFeng, Xin
dc.contributor.authorMuzikansky, Alona
dc.contributor.authorRoss, Alonzo H.
dc.contributor.authorHamblin, Michael R.
dc.contributor.authorJermain, Peter R.
dc.contributor.authorYaroslavsky, Anna N.
dc.date2022-08-11T08:09:53.000
dc.date.accessioned2022-08-23T16:47:48Z
dc.date.available2022-08-23T16:47:48Z
dc.date.issued2019-07-29
dc.date.submitted2019-09-09
dc.identifier.citation<p>Biomed Opt Express. 2019 Jul 29;10(8):4237-4248. doi: 10.1364/BOE.10.004237. eCollection 2019 Aug 1. <a href="https://doi.org/10.1364/BOE.10.004237">Link to article on publisher's site</a></p>
dc.identifier.issn2156-7085 (Linking)
dc.identifier.doi10.1364/BOE.10.004237
dc.identifier.pmid31453007
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41150
dc.description.abstractFluorescence emission, polarization and subcellular localization of methylene blue (MB) were studied in four cancerous and two normal human brain cell lines. Fluorescence emission and polarization images were acquired and analyzed. The co-localization of MB with mitochondria, lysosomes and nuclei of the cells was evaluated. Glioblastoma cells exhibited significantly higher MB fluorescence polarization compared to normal astrocytes. Preferential accumulation of MB in mitochondria of glioblastoma cells may explain higher fluorescence polarization values in cancer cells as compared to normal. These findings may lead to the development of a quantitative method for the detection of brain cancer in single cells.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31453007&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright © 2019 Optical Society of America under the terms of the OSA Open Access Publishing Agreement, https://www.osapublishing.org/submit/review/pdf/OSACopyTransferOAAgrmnt(2017-09-05).pdf.
dc.subjectbrain cancer
dc.subjectglioblastoma cells
dc.subjectcancer cells
dc.subjectdetection of brain cancer
dc.subjectAnalytical, Diagnostic and Therapeutic Techniques and Equipment
dc.subjectBioimaging and Biomedical Optics
dc.subjectCancer Biology
dc.subjectCell Biology
dc.subjectCells
dc.subjectNeoplasms
dc.titleMultimodal quantitative imaging of brain cancer in cultured cells
dc.typeJournal Article
dc.source.journaltitleBiomedical optics express
dc.source.volume10
dc.source.issue8
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4955&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3939
dc.identifier.contextkey15291867
refterms.dateFOA2022-08-23T16:47:48Z
html.description.abstract<p>Fluorescence emission, polarization and subcellular localization of methylene blue (MB) were studied in four cancerous and two normal human brain cell lines. Fluorescence emission and polarization images were acquired and analyzed. The co-localization of MB with mitochondria, lysosomes and nuclei of the cells was evaluated. Glioblastoma cells exhibited significantly higher MB fluorescence polarization compared to normal astrocytes. Preferential accumulation of MB in mitochondria of glioblastoma cells may explain higher fluorescence polarization values in cancer cells as compared to normal. These findings may lead to the development of a quantitative method for the detection of brain cancer in single cells.</p>
dc.identifier.submissionpathoapubs/3939
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages4237-4248


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