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SPARC: a potential target for functional nanomaterials and drugs.
Jiang, Shan; Sun, Hui-Feng; Li, Shuang; Zhang, Ning; Chen, Ji-Song; Liu, Jian-Xin.
Afiliação
  • Jiang S; School of Pharmacy, Heilongjiang University of Traditional Chinese Medicine, Harbin, China.
  • Sun HF; School of Pharmaceutical Sciences, Department of Rehabilitation and Healthcare, Hunan University of Medicine, Huaihua, China.
  • Li S; School of Pharmacy, Heilongjiang University of Traditional Chinese Medicine, Harbin, China.
  • Zhang N; School of Pharmaceutical Sciences, Department of Rehabilitation and Healthcare, Hunan University of Medicine, Huaihua, China.
  • Chen JS; College Pharmacy, Jiamusi University, Jiamusi, China.
  • Liu JX; School of Pharmacy, Heilongjiang University of Traditional Chinese Medicine, Harbin, China.
Front Mol Biosci ; 10: 1235428, 2023.
Article em En | MEDLINE | ID: mdl-37577749
ABSTRACT
Secreted protein acidic and rich in cysteine (SPARC), also termed osteonectin or BM-40, is a matricellular protein which regulates cell adhesion, extracellular matrix production, growth factor activity, and cell cycle. Although SPARC does not perform a structural function, it, however, modulates interactions between cells and the surrounding extracellular matrix due to its anti-proliferative and anti-adhesion properties. The overexpression of SPARC at sites, including injury, regeneration, obesity, cancer, and inflammation, reveals its application as a prospective target and therapeutic indicator in the treatment and assessment of disease. This article comprehensively summarizes the mechanism of SPARC overexpression in inflammation and tumors as well as the latest research progress of functional nanomaterials in the therapy of rheumatoid arthritis and tumors by manipulating SPARC as a new target. This article provides ideas for using functional nanomaterials to treat inflammatory diseases through the SPARC target. The purpose of this article is to provide a reference for ongoing disease research based on SPARC-targeted therapy.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article