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Recent Advances in CXCL12/CXCR4 Antagonists and Nano-Based Drug Delivery Systems for Cancer Therapy.
Zhao, Ruogang; Liu, Jianhao; Li, Zhaohuan; Zhang, Wenhui; Wang, Feng; Zhang, Bo.
Afiliação
  • Zhao R; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
  • Liu J; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
  • Li Z; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
  • Zhang W; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
  • Wang F; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
  • Zhang B; School of Pharmacy, Weifang Medical University, Weifang 261053, China.
Pharmaceutics ; 14(8)2022 Jul 25.
Article em En | MEDLINE | ID: mdl-35893797
ABSTRACT
Chemokines can induce chemotactic cell migration by interacting with G protein-coupled receptors to play a significant regulatory role in the development of cancer. CXC chemokine-12 (CXCL12) can specifically bind to CXC chemokine receptor 4 (CXCR4) and is closely associated with the progression of cancer via multiple signaling pathways. Over recent years, many CXCR4 antagonists have been tested in clinical trials; however, Plerixafor (AMD3100) is the only drug that has been approved for marketing thus far. In this review, we first summarize the mechanisms that mediate the physiological effects of the CXCL12/CXCR4 axis. Then, we describe the use of CXCL12/CXCR4 antagonists. Finally, we discuss the use of nano-based drug delivery systems that exert action on the CXCL12/CXCR4 biological axis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pharmaceutics Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Pharmaceutics Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China