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Antitumor Effect of Platinum-Modified STING Agonist MSA-2.

Mo WangYa CaiTian HeYuhang ZhangLirong YiWenqing LiPeng Zhou
Published in: ACS omega (2024)
The stimulator of interferon genes (STING)-activated innate immune pathway is strong and durable for tumor immunotherapy. MSA-2 is an available non-nucleotide human STING agonist that promotes the tumor immunotherapy of STING activation. However, strategies for remolding and improving the immunotherapy effects of MSA-2 are of value for clinical applications. Here, we synthesized the platinum salt-modified MSA-2 (MSA-2-Pt) due to platinum salt being a classic chemotherapeutic drug. We found that MSA-2-Pt could achieve double-effect antitumor immunotherapy, including inducing cell death by platinum and activating the STING pathway by MSA-2. In the colon carcinoma MC38 model (sensitive to immune checkpoint immunotherapy tumor) and melanoma B16F10 model (poorly immunogenic and highly aggressive tumor), the MSA-2-Pt had a good antitumor effect, which was a little better than MSA-2 with intratumor injections. The results present a promising strategy for STING activation in tumor immunotherapy and broadening platinum-based drugs.
Keyphrases
  • cell death
  • innate immune
  • emergency department
  • signaling pathway
  • dendritic cells
  • immune response
  • genome wide
  • ultrasound guided
  • pi k akt
  • drug induced
  • adverse drug