PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma

PD-L1 expressed on tumor cells contributes to disease progression with evasion from tumor immunity. Plasma cells from multiple myeloma (MM) patients expressed higher levels of PD-L1 compared with healthy volunteers and monoclonal gammopathy of undetermined significance (MGUS) patients, and its expre...

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Main Authors: Hideto Tamura, Mariko Ishibashi, Mika Sunakawa-Kii, Koiti Inokuchi
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/12/4/924
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author Hideto Tamura
Mariko Ishibashi
Mika Sunakawa-Kii
Koiti Inokuchi
author_facet Hideto Tamura
Mariko Ishibashi
Mika Sunakawa-Kii
Koiti Inokuchi
author_sort Hideto Tamura
collection DOAJ
description PD-L1 expressed on tumor cells contributes to disease progression with evasion from tumor immunity. Plasma cells from multiple myeloma (MM) patients expressed higher levels of PD-L1 compared with healthy volunteers and monoclonal gammopathy of undetermined significance (MGUS) patients, and its expression is significantly upregulated in relapsed/refractory patients. Furthermore, high PD-L1 expression is induced by the myeloma microenvironment and PD-L1<sup>+</sup> patients with MGUS and asymptomatic MM tend to show disease progression. PD-L1 expression on myeloma cells was associated with more proliferative potential and resistance to antimyeloma agents because of activation of the Akt pathway through PD-1-bound PD-L1 in MM cells. Those data suggest that PD-L1 plays a crucial role in the disease progression of MM.
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spelling doaj.art-accf204b8f5741eb8fa776fa0231d2822023-11-19T21:11:47ZengMDPI AGCancers2072-66942020-04-0112492410.3390/cancers12040924PD-L1–PD-1 Pathway in the Pathophysiology of Multiple MyelomaHideto Tamura0Mariko Ishibashi1Mika Sunakawa-Kii2Koiti Inokuchi3Division of Diabetes, Endocrinology and Hematology, Department of Internal Medicine, Dokkyo Medical University Saitama Medical Center, Saitama 343-8555, JapanDepartment of Microbiology and Immunology, Nippon Medical School, Tokyo 113-8603, JapanDepartment of Hematology, Nippon Medical School, Tokyo 113-8603, JapanDepartment of Hematology, Nippon Medical School, Tokyo 113-8603, JapanPD-L1 expressed on tumor cells contributes to disease progression with evasion from tumor immunity. Plasma cells from multiple myeloma (MM) patients expressed higher levels of PD-L1 compared with healthy volunteers and monoclonal gammopathy of undetermined significance (MGUS) patients, and its expression is significantly upregulated in relapsed/refractory patients. Furthermore, high PD-L1 expression is induced by the myeloma microenvironment and PD-L1<sup>+</sup> patients with MGUS and asymptomatic MM tend to show disease progression. PD-L1 expression on myeloma cells was associated with more proliferative potential and resistance to antimyeloma agents because of activation of the Akt pathway through PD-1-bound PD-L1 in MM cells. Those data suggest that PD-L1 plays a crucial role in the disease progression of MM.https://www.mdpi.com/2072-6694/12/4/924PD-L1 (B7-H1)PD-1multiple myelomamonoclonal gammopathy of undetermined significance (MGUS)immune checkpoint inhibitorsAKT pathway
spellingShingle Hideto Tamura
Mariko Ishibashi
Mika Sunakawa-Kii
Koiti Inokuchi
PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
Cancers
PD-L1 (B7-H1)
PD-1
multiple myeloma
monoclonal gammopathy of undetermined significance (MGUS)
immune checkpoint inhibitors
AKT pathway
title PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
title_full PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
title_fullStr PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
title_full_unstemmed PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
title_short PD-L1–PD-1 Pathway in the Pathophysiology of Multiple Myeloma
title_sort pd l1 pd 1 pathway in the pathophysiology of multiple myeloma
topic PD-L1 (B7-H1)
PD-1
multiple myeloma
monoclonal gammopathy of undetermined significance (MGUS)
immune checkpoint inhibitors
AKT pathway
url https://www.mdpi.com/2072-6694/12/4/924
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