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Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling

IL30mRNA expression is associated with the TNBC subtype. IL30 boosts proliferation and migration of TNBC cells and reshapes their immunity gene expression profile. The lack of endogenous IL30 hinders TNBC growth and progression and prolongs host survival. TNBC growth inhibition, due to the lack of e...

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Autores principales: Sorrentino, Carlo, Ciummo, Stefania Livia, D'Antonio, Luigi, Lanuti, Paola, Abrams, Scott I., Yin, Zhinan, Lu, Li‐Fan, Di Carlo, Emma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828256/
https://www.ncbi.nlm.nih.gov/pubmed/33635005
http://dx.doi.org/10.1002/ctm2.278
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author Sorrentino, Carlo
Ciummo, Stefania Livia
D'Antonio, Luigi
Lanuti, Paola
Abrams, Scott I.
Yin, Zhinan
Lu, Li‐Fan
Di Carlo, Emma
author_facet Sorrentino, Carlo
Ciummo, Stefania Livia
D'Antonio, Luigi
Lanuti, Paola
Abrams, Scott I.
Yin, Zhinan
Lu, Li‐Fan
Di Carlo, Emma
author_sort Sorrentino, Carlo
collection PubMed
description IL30mRNA expression is associated with the TNBC subtype. IL30 boosts proliferation and migration of TNBC cells and reshapes their immunity gene expression profile. The lack of endogenous IL30 hinders TNBC growth and progression and prolongs host survival. TNBC growth inhibition, due to the lack of endogenous IL30, requires INFγ production by T and NK cells. [Image: see text]
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spelling pubmed-78282562021-02-01 Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling Sorrentino, Carlo Ciummo, Stefania Livia D'Antonio, Luigi Lanuti, Paola Abrams, Scott I. Yin, Zhinan Lu, Li‐Fan Di Carlo, Emma Clin Transl Med Letter to Editor IL30mRNA expression is associated with the TNBC subtype. IL30 boosts proliferation and migration of TNBC cells and reshapes their immunity gene expression profile. The lack of endogenous IL30 hinders TNBC growth and progression and prolongs host survival. TNBC growth inhibition, due to the lack of endogenous IL30, requires INFγ production by T and NK cells. [Image: see text] John Wiley and Sons Inc. 2021-01-24 /pmc/articles/PMC7828256/ /pubmed/33635005 http://dx.doi.org/10.1002/ctm2.278 Text en © 2021 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to Editor
Sorrentino, Carlo
Ciummo, Stefania Livia
D'Antonio, Luigi
Lanuti, Paola
Abrams, Scott I.
Yin, Zhinan
Lu, Li‐Fan
Di Carlo, Emma
Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title_full Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title_fullStr Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title_full_unstemmed Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title_short Hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires IFNγ signaling
title_sort hindering triple negative breast cancer progression by targeting endogenous interleukin‐30 requires ifnγ signaling
topic Letter to Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828256/
https://www.ncbi.nlm.nih.gov/pubmed/33635005
http://dx.doi.org/10.1002/ctm2.278
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