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In vivometal-catalyzed SeCT therapy by a proapoptotic peptide

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dc.contributor.author Ahmadi P.
dc.contributor.author Muguruma K.
dc.contributor.author Chang T.C.
dc.contributor.author Tamura S.
dc.contributor.author Tsubokura K.
dc.contributor.author Egawa Y.
dc.contributor.author Suzuki T.
dc.contributor.author Dohmae N.
dc.contributor.author Nakao Y.
dc.contributor.author Tanaka K.
dc.date.accessioned 2022-02-09T20:46:43Z
dc.date.available 2022-02-09T20:46:43Z
dc.date.issued 2021
dc.identifier.issn 2041-6520
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/170218
dc.description.abstract Selective cell tagging (SeCT) therapy is a strategy for labeling a targeted cell with certain chemical moietiesviaa catalytic chemical transformation in order to elicit a therapeutic effect. Herein, we report a cancer therapy based on targeted cell surface tagging with proapoptotic peptides (Ac-GGKLFG-X; X = reactive group) that induce apoptosis when attached to the cell surface. Using either Au-catalyzed amidation or Ru-catalyzed alkylation, these proapoptotic peptides showed excellent therapeutic effects bothin vitroandin vivo. In particular, co-treatment with proapoptotic peptide and the carrier-Ru complex significantly and synergistically inhibited tumor growth and prolonged survival rate of tumor-bearing mice after only a single injection. This is the first report of Ru catalyst applicationin vivo, and this approach could be used in SeCT for cancer therapy.
dc.relation.ispartofseries Chemical Science
dc.title In vivometal-catalyzed SeCT therapy by a proapoptotic peptide
dc.type Article
dc.relation.ispartofseries-issue 37
dc.relation.ispartofseries-volume 12
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 12266
dc.source.id SCOPUS20416520-2021-12-37-SID85116416695


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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