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

Author

Listed:
  • Shuwei Liang

    (Monash University
    Monash University)

  • Eric Tran

    (Monash University)

  • Xin Du

    (Monash University
    Monash University)

  • Jiajun Dong

    (Purdue University)

  • Harrison Sudholz

    (Monash University
    Monash University)

  • Hao Chen

    (Walter and Eliza Hall Institute of Medical Research
    The University of Melbourne)

  • Zihan Qu

    (Purdue University)

  • Nicholas D. Huntington

    (Monash University
    Monash University)

  • Jeffrey J. Babon

    (Walter and Eliza Hall Institute of Medical Research
    The University of Melbourne)

  • Nadia J. Kershaw

    (Walter and Eliza Hall Institute of Medical Research
    The University of Melbourne)

  • Zhong-Yin Zhang

    (Purdue University
    Purdue University)

  • Jonathan B. Baell

    (Monash University
    South San Francisco)

  • Florian Wiede

    (Monash University
    Monash University)

  • Tony Tiganis

    (Monash University
    Monash University)

Abstract

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.

Suggested Citation

  • 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 , 2023. "A small molecule inhibitor of PTP1B and PTPN2 enhances T cell anti-tumor immunity," Nature Communications, Nature, vol. 14(1), pages 1-27, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-40170-8
    DOI: 10.1038/s41467-023-40170-8
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    References listed on IDEAS

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    1. Robert T. Manguso & Hans W. Pope & Margaret D. Zimmer & Flavian D. Brown & Kathleen B. Yates & Brian C. Miller & Natalie B. Collins & Kevin Bi & Martin W. LaFleur & Vikram R. Juneja & Sarah A. Weiss &, 2017. "In vivo CRISPR screening identifies Ptpn2 as a cancer immunotherapy target," Nature, Nature, vol. 547(7664), pages 413-418, July.
    2. Florian Wiede & Nicole L. La Gruta & Tony Tiganis, 2014. "PTPN2 attenuates T-cell lymphopenia-induced proliferation," Nature Communications, Nature, vol. 5(1), pages 1-15, May.
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    Cited by:

    1. Eduardo H. Gilglioni & Ao Li & Wadsen St-Pierre-Wijckmans & Tzu-Keng Shen & Israel Pérez-Chávez & Garnik Hovhannisyan & Michela Lisjak & Javier Negueruela & Valerie Vandenbempt & Julia Bauzá-Martinez , 2024. "PTPRK regulates glycolysis and de novo lipogenesis to promote hepatocyte metabolic reprogramming in obesity," Nature Communications, Nature, vol. 15(1), pages 1-22, December.

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