The immune system plays a major role in the protection against cancer. Identifying and characterizing the pathways mediating this immune surveillance are thus critical for understanding how cancer cells are recognized and eliminated. Aneuploidy is a hallmark of cancer, and we previously found that untransformed cells that had undergone senescence due to highly abnormal karyotypes are eliminated by natural killer (NK) cells in vitro. However, the mechanisms underlying this process remained elusive. Here, using an in vitro NK cell killing system, we show that non-cell-autonomous mechanisms in aneuploid cells predominantly mediate their clearance by NK cells. Our data indicate that in untransformed aneuploid cells, NF-κB signaling upregulation is central to elicit this immune response. Inactivating NF-κB abolishes NK cell-mediated clearance of untransformed aneuploid cells. In cancer cell lines, NF-κB upregulation also correlates with the degree of aneuploidy. However, such upregulation in cancer cells is not sufficient to trigger NK cell-mediated clearance, suggesting that additional mechanisms might be at play during cancer evolution to counteract NF-κB-mediated immunogenicity.

Aneuploid senescent cells activate NF-κB to promote their immune clearance by NK cells / R.W. Wang, S. Vigano, U. Ben-David, A. Amon, S. Santaguida. - In: EMBO REPORTS. - ISSN 1469-221X. - 22:8(2021 Aug 04), pp. e52032.1-e52032.16. [10.15252/embr.202052032]

Aneuploid senescent cells activate NF-κB to promote their immune clearance by NK cells

S. Vigano;S. Santaguida
Ultimo
Supervision
2021

Abstract

The immune system plays a major role in the protection against cancer. Identifying and characterizing the pathways mediating this immune surveillance are thus critical for understanding how cancer cells are recognized and eliminated. Aneuploidy is a hallmark of cancer, and we previously found that untransformed cells that had undergone senescence due to highly abnormal karyotypes are eliminated by natural killer (NK) cells in vitro. However, the mechanisms underlying this process remained elusive. Here, using an in vitro NK cell killing system, we show that non-cell-autonomous mechanisms in aneuploid cells predominantly mediate their clearance by NK cells. Our data indicate that in untransformed aneuploid cells, NF-κB signaling upregulation is central to elicit this immune response. Inactivating NF-κB abolishes NK cell-mediated clearance of untransformed aneuploid cells. In cancer cell lines, NF-κB upregulation also correlates with the degree of aneuploidy. However, such upregulation in cancer cells is not sufficient to trigger NK cell-mediated clearance, suggesting that additional mechanisms might be at play during cancer evolution to counteract NF-κB-mediated immunogenicity.
English
aneuploidy; complex karyotypes; immune clearance; NF-κB; senescence
Settore BIO/11 - Biologia Molecolare
Articolo
Sì, ma tipo non specificato
Pubblicazione scientifica
4-ago-2021
8-giu-2021
John Wiley and Sons Inc
22
8
e52032
1
16
16
Pubblicato
Periodico con rilevanza internazionale
scopus
orcid
pubmed
crossref
wos
Aderisco
info:eu-repo/semantics/article
Aneuploid senescent cells activate NF-κB to promote their immune clearance by NK cells / R.W. Wang, S. Vigano, U. Ben-David, A. Amon, S. Santaguida. - In: EMBO REPORTS. - ISSN 1469-221X. - 22:8(2021 Aug 04), pp. e52032.1-e52032.16. [10.15252/embr.202052032]
open
Prodotti della ricerca::01 - Articolo su periodico
5
262
Article (author)
si
R.W. Wang, S. Vigano, U. Ben-David, A. Amon, S. Santaguida
File in questo prodotto:
File Dimensione Formato  
embr.202052032.pdf

accesso aperto

Tipologia: Publisher's version/PDF
Dimensione 3.02 MB
Formato Adobe PDF
3.02 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/887126
Citazioni
  • ???jsp.display-item.citation.pmc??? 21
  • Scopus 51
  • ???jsp.display-item.citation.isi??? 52
social impact