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Dual-targeting peptides@PMO, a mimetic to the pro-apoptotic protein Smac/DIABLO for selective activation of apoptosis in cancer cells

Di Giorgio E.
•
Ferino A.
•
Huang W.
altro
De Marco R.
2023
  • journal article

Periodico
FRONTIERS IN PHARMACOLOGY
Abstract
The refractoriness of tumor cells to apoptosis represents the main mechanism of resistance to chemotherapy. Smac/DIABLO mimetics proved to be effective in overcoming cancer-acquired resistance to apoptosis as a consequence of overexpression of the anti-apoptotic proteins XIAP, cIAP1, and cIAP2. In this work, we describe a dual-targeting peptide capable of selectively activating apoptosis in cancer cells. The complex consists of a fluorescent periodic mesoporous organosilica nanoparticle that carries the short sequences of Smac/DIABLO bound to the αvβ3–integrin ligand. The dual-targeting peptide @PMO shows significantly higher toxicity in αvβ3-positive HeLa cells with respect to αvβ3-negative Ht29 cells. @PMO exhibited synergistic effects in combination with oxaliplatin in a panel of αvβ3-positive cancer cells, while its toxicity is overcome by XIAP overexpression or integrin β3 silencing. The successful uptake of the molecule by αvβ3-positive cells makes @PMO promising for the re-sensitization to apoptosis of many cancer types.
DOI
10.3389/fphar.2023.1237478
Archivio
https://hdl.handle.net/11390/1262044
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85170673725
https://ricerca.unityfvg.it/handle/11390/1262044
Diritti
open access
Soggetti
  • caspase

  • cervical cancer

  • colorectal cancer

  • integrin αvβ3

  • nanoparticle

  • oxaliplatin

  • Smac mimetics

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