Biological Function of PD-L2 and Correlation With Overall Survival in Type II Endometrial Cancer.

chemoresistance endometrial cancer immune checkpoint overall survival programmed death ligand 2

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 26 02 2020
accepted: 18 09 2020
entrez: 16 11 2020
pubmed: 17 11 2020
medline: 17 11 2020
Statut: epublish

Résumé

In cancer, upregulation of coinhibitory B7 ligands has been associated with immune evasion. So far, anti-programmed death-1 (PD-1) and anti-PD-ligand 1 (PD-L1) antibodies have been used in immuno-oncology, with promising outcomes; however, it is still needed to identify other markers, especially for endometrial cancer (EC). EC is a gynecological malignancy historically classified into two types: type I, with mostly estrogen-dependent endometrioid diseases, and the most aggressive type II, including mainly estrogen-independent and non-endometrioid tumors. PD ligand-2 (PD-L2) is known as the second ligand of the PD-1 receptor and, upon its binding, contributes to T-cell exhaustion. Up to now, very few information are available about PD-L2 in cancers, and no data have been reported for EC. The aim of this work was to characterize the PD-L1 and PD-L2 ligand expression profile in EC cell lines, focusing the attention on the biological role of PD-L2 and its prognostic impact in human type II EC biopsies. Using

Identifiants

pubmed: 33194598
doi: 10.3389/fonc.2020.538064
pmc: PMC7656062
doi:

Types de publication

Journal Article

Langues

eng

Pagination

538064

Informations de copyright

Copyright © 2020 Marinelli, Annibali, Morelli, Zeppa, Tuyaerts, Aguzzi, Amantini, Maggi, Ferretti, Santoni, Amant and Nabissi.

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Auteurs

Oliviero Marinelli (O)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.
School of Biosciences and Veterinary Medicine, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Daniela Annibali (D)

Gynecological Oncology, Oncology Department and LKI Leuven Cancer Institute, KU Leuven-University of Leuven, Leuven, Belgium.

Maria Beatrice Morelli (MB)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Laura Zeppa (L)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Sandra Tuyaerts (S)

Gynecological Oncology, Oncology Department and LKI Leuven Cancer Institute, KU Leuven-University of Leuven, Leuven, Belgium.

Cristina Aguzzi (C)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Consuelo Amantini (C)

School of Biosciences and Veterinary Medicine, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Federica Maggi (F)

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

Benedetta Ferretti (B)

Medical Oncology Division, San Severino Hospital, Macerata, Italy.

Giorgio Santoni (G)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.

Frédéric Amant (F)

Gynecological Oncology, Oncology Department and LKI Leuven Cancer Institute, KU Leuven-University of Leuven, Leuven, Belgium.
Centre for Gynecologic Oncology Amsterdam (CGOA) Antoni Van Leeuwenhoek-Netherlands Cancer Institute (AvL-NKI) and University Medical Centra (UMC), Amsterdam, Netherlands.

Massimo Nabissi (M)

School of Pharmacy, Experimental Medicine Section, University of Camerino, Camerino, Italy.
Integrative Therapy Discovery Lab, University of Camerino, Camerino, Italy.

Classifications MeSH