Pilot Investigation on p75ICD Expression in Laryngeal Squamous Cell Carcinoma.

ABCG2 CSCs LSCC p75ICD p75NTR tumor invasion

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
25 May 2022
Historique:
received: 14 04 2022
revised: 19 05 2022
accepted: 23 05 2022
entrez: 10 6 2022
pubmed: 11 6 2022
medline: 11 6 2022
Statut: epublish

Résumé

We investigated the p75 Neurotrophin Receptor (p75NTR) expression and cleavage product p75NTR Intracellular Domain (p75ICD) as potential oncogenic and metastatic markers in human Laryngeal Squamous Cell Carcinoma (LSCC). p75NTR is highly expressed in Cancer Stem Cells (CSCs) of the laryngeal epithelia and it has been proposed as a marker for stemness, cell migration, and chemo-resistance in different squamous carcinomas. To investigate the clinical significance of p75NTR cleavage products in solid tumors, full-length and cleaved p75NTR expression was analyzed in laryngeal primary tumors from different-stage LSCC patients, diagnosed at the Policlinico Umberto I Hospital. Molecular and histological techniques were used to detect the expressions of p75NTR and p75ICD, and ATP Binding Cassette Subfamily G Member 2 (ABCG2), a CSC marker. We found regulated p75NTR cleavage during squamous epithelial tumor progression and tissue invasion. Our preliminary investigation suggests p75ICD expression and localization as possible features of tumorigenesis and metastaticity. Its co-localization with ABCG2 in squamous cells in the parenchyma invaded by the tumor formation allows us to hypothesize p75NTR and p75ICD roles in tumor invasion and CSC spreading in LSCC patients. These data might represent a starting point for a comprehensive analysis of p75NTR cleavage and of its clinical relevance as a potential molecular LSCC signature, possibly helping diagnosis, and improving prognosis and personalized therapy.

Identifiants

pubmed: 35681602
pii: cancers14112622
doi: 10.3390/cancers14112622
pmc: PMC9179539
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Sapienza University of Rome
ID : GrandiProgetti 2019

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Auteurs

Viviana Triaca (V)

Institute of Biochemistry and Cell Biology, National Research Council (CNR), International Campus A. Buzzati-Traverso, Monterotondo Scalo, 00015 Rome, Italy.

Elena Fico (E)

Department of Sense Organs, Institute of Biochemistry and Cell Biology, National Research Council (CNR), University of Rome La Sapienza, 00185 Rome, Italy.

Pamela Rosso (P)

Department of Sense Organs, Institute of Biochemistry and Cell Biology, National Research Council (CNR), University of Rome La Sapienza, 00185 Rome, Italy.

Massimo Ralli (M)

Department of Sense Organs, University of Rome La Sapienza, 00185 Rome, Italy.

Alessandro Corsi (A)

Department of Molecular Medicine, University of Rome La Sapienza, 00185 Rome, Italy.

Cinzia Severini (C)

Department of Sense Organs, Institute of Biochemistry and Cell Biology, National Research Council (CNR), University of Rome La Sapienza, 00185 Rome, Italy.

Alvaro Crevenna (A)

Epigenetics and Neurobiology Unit, EMBL Rome, International Campus A. Buzzati-Traverso, Monterotondo Scalo, 00015 Rome, Italy.

Enzo Agostinelli (E)

Department of Sense Organs, University of Rome La Sapienza, 00185 Rome, Italy.

Emma Rullo (E)

Department of Molecular Medicine, University of Rome La Sapienza, 00185 Rome, Italy.

Mara Riminucci (M)

Department of Molecular Medicine, University of Rome La Sapienza, 00185 Rome, Italy.

Andrea Colizza (A)

Department of Sense Organs, University of Rome La Sapienza, 00185 Rome, Italy.

Antonella Polimeni (A)

Department of Oral and Maxillo Facial Sciences, University of Rome La Sapienza, 00185 Rome, Italy.

Antonio Greco (A)

Department of Sense Organs, University of Rome La Sapienza, 00185 Rome, Italy.

Paola Tirassa (P)

Department of Sense Organs, Institute of Biochemistry and Cell Biology, National Research Council (CNR), University of Rome La Sapienza, 00185 Rome, Italy.

Classifications MeSH