A small molecule inhibitor of PTP1B and PTPN2 enhances T cell anti-tumor immunity

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作者
Shuwei Liang
Eric Tran
Xin Du
Jiajun Dong
Harrison Sudholz
Hao Chen
Zihan Qu
Nicholas D. Huntington
Jeffrey J. Babon
Nadia J. Kershaw
Zhong-Yin Zhang
Jonathan B. Baell
Florian Wiede
Tony Tiganis
机构
[1] Monash University,Monash Biomedicine Discovery Institute
[2] Monash University,Department of Biochemistry and Molecular Biology
[3] Monash University,Monash Institute of Pharmaceutical Sciences
[4] Purdue University,Department of Medicinal Chemistry and Molecular Pharmacology
[5] Walter and Eliza Hall Institute of Medical Research,Department of Medical Biology
[6] The University of Melbourne,Department of Chemistry
[7] Purdue University,Lyterian Therapeutics
[8] South San Francisco,undefined
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The inhibition of protein tyrosine phosphatases 1B (PTP1B) and N2 (PTPN2) has emerged as an exciting approach for bolstering T cell anti-tumor immunity. ABBV-CLS-484 is a PTP1B/PTPN2 inhibitor in clinical trials for solid tumors. Here we have explored the therapeutic potential of a related small-molecule-inhibitor, Compound-182. We demonstrate that Compound-182 is a highly potent and selective active site competitive inhibitor of PTP1B and PTPN2 that enhances T cell recruitment and activation and represses the growth of tumors in mice, without promoting overt immune-related toxicities. The enhanced anti-tumor immunity in immunogenic tumors can be ascribed to the inhibition of PTP1B/PTPN2 in T cells, whereas in cold tumors, Compound-182 elicited direct effects on both tumor cells and T cells. Importantly, treatment with Compound-182 rendered otherwise resistant tumors sensitive to α-PD-1 therapy. Our findings establish the potential for small molecule inhibitors of PTP1B and PTPN2 to enhance anti-tumor immunity and combat cancer.
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