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Artikel ; Online: Bcl-xL targeting eliminates ageing tumor-promoting neutrophils and inhibits lung tumor growth.

Bodac, Anita / Mayet, Abdullah / Rana, Sarika / Pascual, Justine / Bowler, Amber D / Roh, Vincent / Fournier, Nadine / Craciun, Ligia / Demetter, Pieter / Radtke, Freddy / Meylan, Etienne

EMBO molecular medicine

2023  Band 16, Heft 1, Seite(n) 158–184

Abstract: Elevated peripheral blood and tumor-infiltrating neutrophils are often associated with a poor patient prognosis. However, therapeutic strategies to target these cells are difficult to implement due to the life-threatening risk of neutropenia. In a ... ...

Abstract Elevated peripheral blood and tumor-infiltrating neutrophils are often associated with a poor patient prognosis. However, therapeutic strategies to target these cells are difficult to implement due to the life-threatening risk of neutropenia. In a genetically engineered mouse model of lung adenocarcinoma, tumor-associated neutrophils (TAN) demonstrate tumor-supportive capacities and have a prolonged lifespan compared to circulating neutrophils. Here, we show that tumor cell-derived GM-CSF triggers the expression of the anti-apoptotic Bcl-xL protein and enhances neutrophil survival through JAK/STAT signaling. Targeting Bcl-xL activity with a specific BH3 mimetic, A-1331852, blocked the induced neutrophil survival without impacting their normal lifespan. Specifically, oral administration with A-1331852 decreased TAN survival and abundance, and reduced tumor growth without causing neutropenia. We also show that G-CSF, a drug used to combat neutropenia in patients receiving chemotherapy, increased the proportion of young TANs and augmented the anti-tumor effect resulting from Bcl-xL blockade. Finally, our human tumor data indicate the same role for Bcl-xL on pro-tumoral neutrophil survival. These results altogether provide preclinical evidence for safe neutrophil targeting based on their aberrant intra-tumor longevity.
Mesh-Begriff(e) Animals ; Humans ; Mice ; Aging ; Apoptosis ; Apoptosis Regulatory Proteins/metabolism ; bcl-X Protein ; Cell Line, Tumor ; Lung Neoplasms/pathology ; Neutropenia/drug therapy ; Neutropenia/metabolism ; Neutropenia/pathology ; Neutrophils/metabolism
Chemische Substanzen Apoptosis Regulatory Proteins ; bcl-X Protein ; Bcl2l1 protein, mouse
Sprache Englisch
Erscheinungsdatum 2023-12-20
Erscheinungsland England
Dokumenttyp Journal Article
ZDB-ID 2467145-9
ISSN 1757-4684 ; 1757-4676
ISSN (online) 1757-4684
ISSN 1757-4676
DOI 10.1038/s44321-023-00013-x
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Zs.A 6784: Hefte anzeigen Standort:
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ab Jg. 2022: Lesesaal (EG)
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