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Authors Guo PD, Sun ZW, Lai HJ, Yang J, Wu PP, Guo YD, Sun J
Received 15 June 2018
Accepted for publication 15 August 2018
Published 1 November 2018 Volume 2018:11 Pages 7635—7642
DOI https://doi.org/10.2147/OTT.S177329
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Andrew Yee
Peer reviewer comments 2
Editor who approved publication: Dr Sanjeev Srivastava
Background: (PD-L2), a ligand of programmed cell death protein 1 (PD-1), is an
inhibitory receptor of T cells and activated B cells. Many studies have focused
on PD-L1, another ligand of PD-1, and the prognostic significance of PD-L1 has
been reported in many tumors. However, the expression of PD-L2 in relation to
clinical outcomes has not been fully investigated in cancer patients.
Patients and
methods: In this study, we investigated the
expression of PD-L2 via immunohistochemistry (IHC) in the pathological
specimens of 348 patients treated for colorectal cancer (CRC).
Results: Strong PD-L2 expression was found in the cancer tissues from 41%
of the CRC patients who also had a high TNM stage and carcinoembryonic antigen
(CEA) concentration. We also carried out functional studies in vitro, which
showed that PD-L2 did not influence the growth of the CRC cell line HCT116, but
increased cell invasion.
Conclusion: Collectively, these findings suggest that PD-L2 may be a potential
therapeutic target for CRC.
Keywords: PD-L2, colorectal cancer, migration, therapeutic target