Spotlight on PSMA as a new theranostic biomarker for bladder cancer.
Adult
Aged
Aged, 80 and over
Antigens, Surface
/ biosynthesis
Biomarkers, Tumor
/ biosynthesis
Female
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
Glutamate Carboxypeptidase II
/ biosynthesis
Humans
Male
Middle Aged
Neoplasm Proteins
/ biosynthesis
Retrospective Studies
Urinary Bladder Neoplasms
/ metabolism
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
07 05 2021
07 05 2021
Historique:
received:
10
12
2020
accepted:
14
04
2021
entrez:
8
5
2021
pubmed:
9
5
2021
medline:
25
2
2023
Statut:
epublish
Résumé
Bladder cancer (BCa) patients are diagnosed by cytology and cystoscopy. However, these diagnostic tests bear some limitations. We sought for reliable biomarkers to better determine BCa extension. Prostate-specific membrane antigen (PSMA) appears to fulfill this requirement in prostate cancer but its role in BCa has not been established yet. We then analyzed 87 bladder tissue samples from 74 patients assessing PSMA expression by immunohistochemistry. The median PSMA expression, exclusively found in tumor neovasculature, in terms of H-score significantly differed between non-tumor samples and tumor samples (p = 0.00288) showing a higher neovasculature-related PSMA expression. No differences were observed in relation to tumor type, grade and stage. BCa neovasculature-related PSMA overexpression may be useful in defining the degree of extension of the neoplasm. In addition, testing PSMA expression by immunohistochemistry may hold theranostic implications both considering anti-angiogenesis agents and radio-labelled PSMA ligands for intracavitary radionuclide therapy. In our opinion, BCa neovasculature-related PSMA overexpression may be considered an apt target for anti-angiogenesis and radionuclide treatment in BCa, once the evaluation of tumor-retention time for the appropriateness of long half-life therapeutic PSMA ligands as radionuclide treatment will be performed.
Identifiants
pubmed: 33963223
doi: 10.1038/s41598-021-89160-0
pii: 10.1038/s41598-021-89160-0
pmc: PMC8105396
doi:
Substances chimiques
Antigens, Surface
0
Biomarkers, Tumor
0
Neoplasm Proteins
0
FOLH1 protein, human
EC 3.4.17.21
Glutamate Carboxypeptidase II
EC 3.4.17.21
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
9777Références
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