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Science
Article . 2016
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Chemotherapy-induced antitumor immunity requires formyl peptide receptor 1

Authors: Vacchelli Erika; Ma Yuting; Baracco Elisa E; Sistigu Antonella; Enot David P; Pietrocola Federico; Yang Heng; +35 Authors

Chemotherapy-induced antitumor immunity requires formyl peptide receptor 1

Abstract

How dying tumor cells get noticed Besides killing tumor cells directly, some chemotherapies, such as anthracyclines, also activate the immune system to kill tumors. Vacchelli et al. discovered that in mice, anthracycline-induced antitumor immunity requires immune cells to express the protein formyl peptide receptor 1 (FPR1). Dendritic cells (DCs) near tumors expressed especially high amounts of FPR1. DCs normally capture fragments of dying tumor cells and use them to activate nearby T cells to kill tumors, but DCs lacking FPR1 failed to do this effectively. Individuals with breast or colon cancer expressing a variant of FPR1 and treated with anthracyclines showed poor metastasis-free and overall survival. Thus, FPR1 may affect anti-tumor immunity in people, too. Science , this issue p. 972

Country
Italy
Keywords

T-Lymphocytes, Breast Neoplasms, microfluidic chip, chemotherapy, Polymorphism, Single Nucleotide, immune response, Mice, Cell Line, Tumor, Neoplasms, Leukocytes, Animals, Humans, Anthracyclines, dendritic cells; anthracycline chemotherapy; FPR1, Alleles, Annexin A1, Dendritic Cells, Receptors, Formyl Peptide, Immunity, Innate, Chemotherapy, Adjuvant, Female, Colorectal Neoplasms, FPR1 microfluidic

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    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    424
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 0.1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 1%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
424
Top 0.1%
Top 1%
Top 0.1%
Green
bronze