eEF2K promotes PD-L1 stabilization through inactivating GSK3β in melanoma.


Journal

Journal for immunotherapy of cancer
ISSN: 2051-1426
Titre abrégé: J Immunother Cancer
Pays: England
ID NLM: 101620585

Informations de publication

Date de publication:
03 2022
Historique:
accepted: 03 03 2022
entrez: 29 3 2022
pubmed: 30 3 2022
medline: 15 4 2022
Statut: ppublish

Résumé

Immune checkpoint blockade (ICB) targeting programmed death ligand-1 (PD-L1)/programmed cell death protein-1 (PD-1) pathway has become an attractive strategy for cancer treatment; however, unsatisfactory efficacy has limited its clinical benefits. Therefore, a more comprehensive understanding of the regulation of PD-L1 expression is essential for developing more effective cancer immunotherapy. Recent studies have revealed the important roles of eukaryotic elongation factor 2 kinase (eEF2K) in promoting epithelial-mesenchymal transition (EMT), angiogenesis, tumor cell migration and invasion; nevertheless, the exact role of eEF2K in the regulation of tumor immune microenvironment (TIME) remains largely unknown. In this study, we used a cohort of 38 patients with melanoma who received anti-PD-1 treatment to explore the association between eEF2K expression and immunotherapy efficacy against melanoma. Immunoprecipitation-mass spectrometry analysis and in vitro assays were used to examine the role and molecular mechanism of eEF2K in regulating PD-L1 expression. We also determined the effects of eEF2K on tumor growth and cytotoxicity of CD8 High eEF2K expression is correlated with better therapeutic response and longer survival in patients with melanoma treated with PD-1 monoclonal antibody (mAb). Moreover, eEF2K protein expression is positively correlated with PD-L1 protein expression. Mechanistically, eEF2K directly bound to and inactivated glycogen synthase kinase 3 beta (GSK3β) by phosphorylating it at serine 9 (S9), leading to PD-L1 protein stabilization and upregulation, and subsequently tumor immune evasion. Knockdown of eEF2K decreased PD-L1 expression and enhanced CD8 Our results suggest that eEF2K may serve as a biomarker for predicting therapeutic response and prognosis in patients receiving anti-PD-1 therapy, reveal a vital role of eEF2K in regulating TIME by controlling PD-L1 expression and provide a potential combination therapeutic strategy of eEF2K inhibition with ICB therapy.

Sections du résumé

BACKGROUND
Immune checkpoint blockade (ICB) targeting programmed death ligand-1 (PD-L1)/programmed cell death protein-1 (PD-1) pathway has become an attractive strategy for cancer treatment; however, unsatisfactory efficacy has limited its clinical benefits. Therefore, a more comprehensive understanding of the regulation of PD-L1 expression is essential for developing more effective cancer immunotherapy. Recent studies have revealed the important roles of eukaryotic elongation factor 2 kinase (eEF2K) in promoting epithelial-mesenchymal transition (EMT), angiogenesis, tumor cell migration and invasion; nevertheless, the exact role of eEF2K in the regulation of tumor immune microenvironment (TIME) remains largely unknown.
METHODS
In this study, we used a cohort of 38 patients with melanoma who received anti-PD-1 treatment to explore the association between eEF2K expression and immunotherapy efficacy against melanoma. Immunoprecipitation-mass spectrometry analysis and in vitro assays were used to examine the role and molecular mechanism of eEF2K in regulating PD-L1 expression. We also determined the effects of eEF2K on tumor growth and cytotoxicity of CD8
RESULTS
High eEF2K expression is correlated with better therapeutic response and longer survival in patients with melanoma treated with PD-1 monoclonal antibody (mAb). Moreover, eEF2K protein expression is positively correlated with PD-L1 protein expression. Mechanistically, eEF2K directly bound to and inactivated glycogen synthase kinase 3 beta (GSK3β) by phosphorylating it at serine 9 (S9), leading to PD-L1 protein stabilization and upregulation, and subsequently tumor immune evasion. Knockdown of eEF2K decreased PD-L1 expression and enhanced CD8
CONCLUSIONS
Our results suggest that eEF2K may serve as a biomarker for predicting therapeutic response and prognosis in patients receiving anti-PD-1 therapy, reveal a vital role of eEF2K in regulating TIME by controlling PD-L1 expression and provide a potential combination therapeutic strategy of eEF2K inhibition with ICB therapy.

Identifiants

pubmed: 35347072
pii: jitc-2021-004026
doi: 10.1136/jitc-2021-004026
pmc: PMC8961175
pii:
doi:

Substances chimiques

Antibodies, Monoclonal 0
B7-H1 Antigen 0
CD274 protein, human 0
Programmed Cell Death 1 Receptor 0
EEF2K protein, human EC 2.7.1.17
Glycogen Synthase Kinase 3 beta EC 2.7.11.1
Eef2k protein, mouse EC 2.7.11.20
Elongation Factor 2 Kinase EC 2.7.11.20

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Xisha Chen (X)

Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Hunan Provincial Engineering Research Centre of Translational Medicine and Innovative Drug, Changsha, China.

Kuansong Wang (K)

Department of Pathology, Xiangya hospital and Department of Pathology, School of Basic Medicine, Central South University, Changsha, China.

Shilong Jiang (S)

Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.

Hongyin Sun (H)

Department of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, China.

Xuanling Che (X)

Department of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, China.

Minghui Zhang (M)

Department of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin, China.

Jiaying He (J)

Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.

Ying Wen (Y)

Department of General Surgery, The Second Xiangya Hospital, Central South University, Changsha, China.

Mengting Liao (M)

Department of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, China.

Xiangling Li (X)

Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China.
Hunan Provincial Engineering Research Centre of Translational Medicine and Innovative Drug, Changsha, China.

Xiaoming Zhou (X)

Department of Pharmacy, School of Medicine, Hunan Normal University, Changsha, China.

Jianxun Song (J)

Department of Microbial Pathogenesis and Immunology, Texas A&M University Health Science Center, Bryan, Texas, USA.

Xingcong Ren (X)

Department of Cancer Biology and Toxicology, Department of Pharmacology, College of Medicine, Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA.

Wenjun Yi (W)

Department of General Surgery, The Second Xiangya Hospital, Central South University, Changsha, China.

Jinming Yang (J)

Department of Cancer Biology and Toxicology, Department of Pharmacology, College of Medicine, Markey Cancer Center, University of Kentucky, Lexington, Kentucky, USA.

Xiang Chen (X)

Department of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, China yancheng@csu.edu.cn yinmingzhu2008@126.com chenxiangck@126.com.

Mingzhu Yin (M)

Department of Dermatology, Hunan Engineering Research Center of Skin Health and Disease, Hunan Key Laboratory of Skin Cancer and Psoriasis, Xiangya Hospital, Central South University, Changsha, China yancheng@csu.edu.cn yinmingzhu2008@126.com chenxiangck@126.com.

Yan Cheng (Y)

Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, China yancheng@csu.edu.cn yinmingzhu2008@126.com chenxiangck@126.com.
Hunan Provincial Engineering Research Centre of Translational Medicine and Innovative Drug, Changsha, China.

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