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Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts.

Xin LiTu-Ying YongZhaohan WeiNana BieXiaoqiong ZhangGuiting ZhanJianye LiJiaqi QinJingjing YuBixiang ZhangLu GanXiangliang Yang
Published in: Nature communications (2022)
Insufficient tumor accumulation and distribution of photosensitizers as well as low antitumor immunity severely restrict the therapeutic efficacy of photothermal therapy (PTT). Cancer-associated fibroblasts (CAFs) play a key role in tumor extracellular matrix (ECM) remodeling and immune evasion. Reshaping tumor microenvironment via CAF regulation might provide a potential approach for complete tumor elimination in combination with PTT. Here, tumor cell-derived microparticles co-delivering calcipotriol and Indocyanine green (Cal/ICG@MPs) are developed to modulate CAFs for improved PTT efficacy. Cal/ICG@MPs efficiently target tumor tissues and regulate CAFs to reduce tumor ECM, resulting in enhanced tumor accumulation and penetration of ICG to generate strong PTT efficacy and activate CD8 + T cell-mediated antitumor immunity. In addition, Cal/ICG@MPs-triggered CAF regulation enhances tumor infiltration of CD8 + T cells and ameliorates CAF-induced antigen-mediated activation-induced cell death of tumor-specific CD8 + T cells in response to PTT, eliciting long-term antitumor immune memory to inhibit tumor recurrence and metastasis. Our results support Cal/ICG@MPs as a promising drug to improve PTT efficacy in cancer treatment.
Keyphrases
  • cell death
  • gene expression
  • oxidative stress
  • endothelial cells
  • fluorescence imaging
  • photodynamic therapy
  • signaling pathway
  • climate change