PreS1 peptide-functionalized gold nanostructures with SERRS tags for efficient liver cancer cell targeting.


Journal

Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109

Informations de publication

Date de publication:
Oct 2019
Historique:
received: 23 01 2019
revised: 10 05 2019
accepted: 15 05 2019
entrez: 28 7 2019
pubmed: 28 7 2019
medline: 31 12 2019
Statut: ppublish

Résumé

Early detection is the most effective mean of improving prognosis for many fatal diseases such as cancer. In this context, the Surface Enhanced Resonance Raman Scattering (SERRS) technique is being proposed as alternative to fluorescent methods in detection of biomarkers, because SERRS nanostructures are bright as fluorescent tags but more stable and clearly detectable using the narrow Raman "fingerprints" of a suitable reporter. Here we show that biocompatible SERRS active gold nanostructures, functionalized with an engineered PreS1 peptide (AuNP@PEG-PreS1), detect the presence of the SerpinB3 antigen overexpressed on liver tumor cells, a biomarker of the onset of liver cell carcinomatous transformation. A proper engineering of the targeting unit, linked to the nanostructure by a polymer chain, affords a sensitivity and specificity larger than 80%, at subnanomolar concentrations. Taking into account the high sensitivity of SERRS and that SB3 overexpression is an early event in liver cell carcinomatous transformation, AuNP@PEG-PreS1 nanostructures could be used in routine diagnostic activities, to improve the accuracy of HCC detection in particular in patients with chronic liver diseases.

Identifiants

pubmed: 31349478
pii: S0928-4931(19)30285-1
doi: 10.1016/j.msec.2019.109762
pii:
doi:

Substances chimiques

Antigens, Neoplasm 0
Hepatitis B Surface Antigens 0
Neoplasm Proteins 0
Peptides 0
Protein Precursors 0
Serpins 0
presurface protein 1, hepatitis B surface antigen 0
squamous cell carcinoma-related antigen 0
Gold 7440-57-5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109762

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Francesca Biscaglia (F)

Department of Chemical Sciences, University of Padova, via F. Marzolo 1, 35131 Padova, Italy.

Santina Quarta (S)

Department of Medicine, University of Padova, via N. Giustiniani 2, 35128 Padova, Italy.

Gianmarco Villano (G)

Department of Oncological and Gastroenterological Surgical Sciences, University of Padova, via N. Giustiniani 2, 35128 Padova, Italy.

Cristian Turato (C)

Veneto Institute of Oncology IOV - IRCCS, via Gattamelata 64, 35128 Padova, Italy.

Alessandra Biasiolo (A)

Department of Medicine, University of Padova, via N. Giustiniani 2, 35128 Padova, Italy.

Lucio Litti (L)

Department of Chemical Sciences, University of Padova, via F. Marzolo 1, 35131 Padova, Italy.

Maria Ruzzene (M)

Department of Biomedical Sciences, University of Padova, via U. Bassi 58/b, 35131 Padova, Italy.

Moreno Meneghetti (M)

Department of Chemical Sciences, University of Padova, via F. Marzolo 1, 35131 Padova, Italy.

Patrizia Pontisso (P)

Department of Medicine, University of Padova, via N. Giustiniani 2, 35128 Padova, Italy. Electronic address: patrizia@unipd.it.

Marina Gobbo (M)

Department of Chemical Sciences, University of Padova, via F. Marzolo 1, 35131 Padova, Italy. Electronic address: marina.gobbo@unipd.it.

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Classifications MeSH