Abstract

The expression of PD-L1 in tumor cells is one of the main causes of tumor immune escape. However, the exact mechanism for regulating PD-L1 expression in gastric cancer (GC) cells remains unclear. Our previous studies have shown that mesenchymal stem cells (MSCs) exert broad immunosuppressive potential, modulating the activity of cells either in innate or adaptive immune system to promote tumor progress. This study aims to investigate whether GCMSCs regulate the PD-L1 expression in GC cells and explore the specific molecular mechanism. The results have shown that GCMSCs enhanced PD-L1 expression in GC cells resulting in the resistance of GC cells to CD8+ T cells cytotoxicity. However, this resistance was attenuated with IL-8 inhibition. Further studies proved that IL-8 derived from GCMSCs induced PD-L1 expression in GC cells via c-Myc regulated by STAT3 and mTOR signaling pathways. Our data indicated that blocking IL-8 derived from GCMSCs may overcome the immune escape induced by PD-L1 in GC cells and provide a potential strategy to enhance the immunotherapy efficiency in GC.

Details

Title
Gastric cancer mesenchymal stem cells derived IL-8 induces PD-L1 expression in gastric cancer cells via STAT3/mTOR-c-Myc signal axis
Author
Sun, Li 1 ; Wang, Qianqian 1 ; Chen, Bin 1 ; Zhao, Yuanyuan 1 ; Shen, Bo 2 ; Wang, Hua 3 ; Xu, Jing 3 ; Zhu, Miaolin 2 ; Zhao, Xiangdong 4 ; Xu, Changgen 4 ; Chen, Zhihong 5 ; Wang, Mei 1 ; Xu, Wenrong 1 ; Zhu, Wei 1 

 School of Medicine, Jiangsu University, Zhenjiang, Jiangsu, China 
 Department of oncology, Jiangsu Cancer Hospital Affiliated to Nanjing Medical University, Nanjing, Jiangsu, China 
 Affiliated Hospital of Jiangsu University, Zhenjiang, Jiangsu, China 
 Zhenjiang Provincial Blood Center, Zhenjiang, Jiangsu, China 
 Department of Gastrointestinal Surgery, Affiliated People’s Hospital of Jiangsu University, Zhenjiang, Jiangsu, China 
Pages
1-11
Publication year
2018
Publication date
Sep 2018
Publisher
Springer Nature B.V.
e-ISSN
20414889
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2102377422
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.