4.7 Article

Hematopoietic Progenitor Kinase 1 in Tumor Immunology: A Medicinal Chemistry Perspective

期刊

JOURNAL OF MEDICINAL CHEMISTRY
卷 65, 期 12, 页码 8065-8090

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.2c00172

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资金

  1. National Natural Science Foundation of China [82073766, 81872737, 81930100]
  2. Foundation Research Project of Jiangsu Province [BK20201331]
  3. Double First Class Innovation Team [CPU2018GY02]
  4. China Pharmaceutical University [2632022YC05]
  5. Project Program of State Key Laboratory of Natural Medicines, China Pharmaceutical University [SKLNMZZ202003]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions
  7. Qinglan Project of Jiangsu Province

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HPK1, a negative regulator of immune cells, has emerged as a promising target for tumor immunotherapy. Inhibitors and PROTACs targeting HPK1 have been developed to enhance immune response and inhibit tumor growth.
Hematopoietic progenitor kinase 1 (HPK1), a hematopoietic cell-restricted member of the serine/threonine Ste20-related protein kinases, is a negative regulator of the T cell receptor, B cell receptor, and dendritic cells. Loss of HPK1 kinase function increases cytokine secretion and enhances T cell signaling, virus clearance, and tumor growth inhibition. Therefore, HPK1 is considered a promising target for tumor immunotherapy. Several HPK1 inhibitors have been reported to regulate T cell function. In addition, HPK1-targeting PROTACs, which can induce the degradation of HPK1, have also been developed. Here, we provide an overview of research concerning HPK1 protein structure, function, and inhibitors and propose perspectives and insights for the future development of agents targeting HPK1.

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