Unknown

Dataset Information

0

Deglycosylation of PD-L1 by 2-deoxyglucose reverses PARP inhibitor-induced immunosuppression in triple-negative breast cancer.


ABSTRACT: Triple-negative breast cancer (TNBC), the most difficult-to-treat breast cancer subtype, lacks well-defined molecular targets. TNBC has increased programmed death-ligand 1 (PD-L1) expression, and its immunosuppressive nature makes it suitable for immune checkpoint blockade therapy. However, the response rate of TNBC to anti-PD-L1 or anti-programmed cell death protein 1 (PD-1) therapy remains unsatisfactory, as only 10-20% of TNBC patients have a partial response. Glycosylated PD-L1, the functional form of PD-L1, is required for PD-L1-PD-1 interaction. TNBC cells have significantly higher levels of glycosylated PD-L1 than non-TNBC cells do. In a screening of glucose analogs to block PD-L1 glycosylation, we found that 2-deoxyglucose (2-DG) can act as a glucose analog to decrease PD-L1 glycosylation. Because PARP inhibition upregulates PD-L1, 2-DG reduced PARP inhibition-mediated expression of glycosylated PD-L1. The combination of PARP inhibition and 2-DG had potent anti-tumor activity. Together, our results provide a strong rationale for investigating the targeting of PD-L1 glycosylation in TNBC further.

SUBMITTER: Shao B 

PROVIDER: S-EPMC6176188 | biostudies-literature | 2018

REPOSITORIES: biostudies-literature

altmetric image

Publications

Deglycosylation of PD-L1 by 2-deoxyglucose reverses PARP inhibitor-induced immunosuppression in triple-negative breast cancer.

Shao Bin B   Li Chia-Wei CW   Lim Seung-Oe SO   Sun Linlin L   Lai Yun-Ju YJ   Hou Junwei J   Liu Chunxiao C   Chang Chiung-Wen CW   Qiu Yufan Y   Hsu Jung-Mao JM   Chan Li-Chuan LC   Zha Zhengyu Z   Li Huiping H   Hung Mien-Chie MC  

American journal of cancer research 20180901 9


Triple-negative breast cancer (TNBC), the most difficult-to-treat breast cancer subtype, lacks well-defined molecular targets. TNBC has increased programmed death-ligand 1 (PD-L1) expression, and its immunosuppressive nature makes it suitable for immune checkpoint blockade therapy. However, the response rate of TNBC to anti-PD-L1 or anti-programmed cell death protein 1 (PD-1) therapy remains unsatisfactory, as only 10-20% of TNBC patients have a partial response. Glycosylated PD-L1, the function  ...[more]

Similar Datasets

| S-EPMC6511636 | biostudies-literature
| S-EPMC5511572 | biostudies-literature
| S-EPMC6448063 | biostudies-literature
| S-EPMC7539780 | biostudies-literature
| S-EPMC4000553 | biostudies-literature
| S-EPMC9862087 | biostudies-literature
| S-EPMC10055616 | biostudies-literature
| S-EPMC5176643 | biostudies-literature
| S-EPMC10778345 | biostudies-literature
| S-EPMC9110638 | biostudies-literature