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Targeting GPRC5D for multiple myeloma therapy.
Zhou, Dian; Wang, Ying; Chen, Chong; Li, Zhenyu; Xu, Kailin; Zhao, Kai.
Afiliación
  • Zhou D; Department of Hematology, Affiliated Hospital of Xuzhou Medical University, #99 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
  • Wang Y; Blood Diseases Institute, Xuzhou Medical University, #84 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
  • Chen C; Department of Hematology, Affiliated Hospital of Xuzhou Medical University, #99 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
  • Li Z; Blood Diseases Institute, Xuzhou Medical University, #84 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
  • Xu K; Department of Hematology, Affiliated Hospital of Xuzhou Medical University, #99 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
  • Zhao K; Blood Diseases Institute, Xuzhou Medical University, #84 West Huaihai Road, Xuzhou, 221002, Jiangsu, China.
J Hematol Oncol ; 17(1): 88, 2024 Sep 28.
Article en En | MEDLINE | ID: mdl-39342286
ABSTRACT
Given its nearly ubiquitous expression on plasma cells and limited expression on essential normal tissue, the G protein-coupled receptor class C group 5 member D (GPRC5D) presents a promising opportunity for utilization as an immunotherapy target in multiple myeloma (MM). The therapeutic strategies targeting GPRC5D, such as bispecific antibodies (BsAbs), chimeric antigen receptor (CAR) T cells, and antibody-drug conjugates (ADCs), have been prominently emphasized in relapsed/refractory MM (R/R MM) in recent years. Further clinical trials are necessary to confirm the long-term efficacy of GPRC5D-targeting immunotherapies alone, explore their potentials co-targeting with other specific antigens, or investigate their combinations with existing treatments to overcome MM resistance. This review provides an overview of current research progress in GPRC5D, encompassing its biological characteristics and translational journey from laboratory to clinical application.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores Acoplados a Proteínas G / Mieloma Múltiple Límite: Animals / Humans Idioma: En Revista: J Hematol Oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores Acoplados a Proteínas G / Mieloma Múltiple Límite: Animals / Humans Idioma: En Revista: J Hematol Oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido