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Nutrient-delivery and metabolism reactivation therapy for melanoma

  • Yang Chen
  • , Chaochao Wang
  • , Yelin Wu
  • , Ya Wang
  • , Yun Meng
  • , Fan Wu
  • , Huilin Zhang
  • , Yuen Yee Cheng
  • , Xingwu Jiang
  • , Jieyun Shi
  • , Huiyan Li
  • , Peiran Zhao
  • , Jinfeng Wu*
  • , Bin Zheng
  • , Dayong Jin*
  • , Wenbo Bu*
  • *此作品的通讯作者
  • Tongji University
  • Fudan University
  • University of Technology Sydney
  • Cedars-Sinai Medical Center
  • Eastern Institute of Technology, Ningbo

科研成果: 期刊稿件文章同行评审

摘要

To fulfil the demands of rapid proliferation, tumour cells undergo significant metabolic alterations. Suppression of hyperactivated metabolism has been proven to counteract tumour growth. However, whether the reactivation of downregulated metabolic pathways has therapeutic effects remains unexplored. Here we report a nutrient-based metabolic reactivation strategy for effective melanoma treatment. l-Tyrosine–oleylamine nanomicelles (MTyr–OANPs) were constructed for targeted supplementation of tyrosine to reactivate melanogenesis in melanoma cells. We found that reactivation of melanogenesis using MTyr–OANPs significantly impeded the proliferation of melanoma cells, primarily through the inhibition of glycolysis. Furthermore, leveraging melanin as a natural photothermal reagent for photothermal therapy, we demonstrated the complete eradication of tumours in B16F10 melanoma-bearing mice through treatment with MTyr–OANPs and photothermal therapy. Our strategy for metabolism activation-based tumour treatment suggests specific nutrients as potent activators of metabolic pathways.

源语言英语
页(从-至)1399-1408
页数10
期刊Nature Nanotechnology
19
9
DOI
出版状态已出版 - 9月 2024
已对外发布

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