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Flow cytometry-based immunophenotyping of myeloid-derived suppressor cells in human breast cancer patient blood samples

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dc.contributor.authorLee, Eun Jung-
dc.contributor.authorJung, Seungpil-
dc.contributor.authorPark, Kyong Hwa-
dc.contributor.authorPark, Serk In-
dc.date.accessioned2022-11-17T13:41:10Z-
dc.date.available2022-11-17T13:41:10Z-
dc.date.created2022-11-17-
dc.date.issued2022-11-
dc.identifier.issn0022-1759-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/145644-
dc.description.abstractMulti-color flow cytometry is the standard approach for immunophenotyping clinical samples. With the recent advances in cancer immunotherapy, myeloid-derived suppressor cells (MDSC), immature myeloid-lineage cells in cancer patient blood and the tumor microenvironment, are highlighted as an important immune cell population that correlates with prognosis and therapeutic efficacy. In contrast to their clear functions and existence, immunophenotyping of MDSC is not consistent among investigators due to surface antigens overlapping with many normal hematopoietic lineage cell populations. We performed a clinical study and analyzed more than 1000 breast cancer patients blood samples to quantitate MDSC during breast cancer progression. In this meth-odology manuscript, we described detailed procedures for study design, sample logistics and handling, staining and flow cytometric analysis. This protocol used a 7-color fluorochrome-conjugated antibody panel to analyze polymorphonuclear (PMN)-and monocytic (M)-MDSC subsets simultaneously. The interim analysis results of this study showed that both PMN and M-MDSC populations are increased in patients with bone metastasis compared with patients with visceral organ metastasis. In conclusion, this work provides a versatile, comprehensive, and practical protocol to measure MDSC in patient blood samples.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.titleFlow cytometry-based immunophenotyping of myeloid-derived suppressor cells in human breast cancer patient blood samples-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Serk In-
dc.identifier.doi10.1016/j.jim.2022.113348-
dc.identifier.scopusid2-s2.0-85137894423-
dc.identifier.wosid000861119200002-
dc.identifier.bibliographicCitationJOURNAL OF IMMUNOLOGICAL METHODS, v.510-
dc.relation.isPartOfJOURNAL OF IMMUNOLOGICAL METHODS-
dc.citation.titleJOURNAL OF IMMUNOLOGICAL METHODS-
dc.citation.volume510-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordAuthorMyeloid -derived suppressor cells-
dc.subject.keywordAuthorFlow cytometry-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorBlood-
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