LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma. - Institut de Neurophysiopathologie Accéder directement au contenu
Article Dans Une Revue Communications Biology Année : 2021

LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma.

Angélina Acier
Magali Godard
  • Fonction : Auteur
Fanny Gassiot
  • Fonction : Auteur
Pascal Finetti
Marion Rubis
  • Fonction : Auteur
Jonathan Nowak
  • Fonction : Auteur
Juan Iovanna
Richard Tomasini
Pascaline Lécorché
  • Fonction : Auteur
Guillaume Jacquot
  • Fonction : Auteur
Jamal Temsamani
  • Fonction : Auteur
Cédric Malicet
  • Fonction : Auteur
Sophie Vasseur
Fabienne Guillaumond

Résumé

Despite clinical advances in diagnosis and treatment, pancreatic ductal adenocarcinoma (PDAC) remains the third leading cause of cancer death, and is still associated with poor prognosis and dismal survival rates. Identifying novel PDAC-targeted tools to tackle these unmet clinical needs is thus an urgent requirement. Here we use a peptide conjugate that specifically targets PDAC through low-density lipoprotein receptor (LDLR). We demonstrate by using near-infrared fluorescence imaging the potential of this conjugate to specifically detect and discriminate primary PDAC from healthy organs including pancreas and from benign mass-forming chronic pancreatitis, as well as detect metastatic pancreatic cancer cells in healthy liver. This work paves the way towards clinical applications in which safe LDLR-targeting peptide conjugate promotes tumor-specific delivery of imaging and/or therapeutic agents, thereby leading to substantial improvements of the PDAC patient’s outcome.
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Dates et versions

hal-03452855 , version 1 (09-02-2022)

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Angélina Acier, Magali Godard, Fanny Gassiot, Pascal Finetti, Marion Rubis, et al.. LDL receptor-peptide conjugate as in vivo tool for specific targeting of pancreatic ductal adenocarcinoma.. Communications Biology, 2021, 4 (1), pp.987. ⟨10.1038/s42003-021-02508-0⟩. ⟨hal-03452855⟩
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