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A nanodrug incorporating siRNA PD-L1 and Birinapant for enhancing tumor immunotherapy.

Tingting GongYu-Jun CaiFengze SunJiaxin ChenZhongzhen SuXin-Tao ShuaiHong Shan
Published in: Biomaterials science (2021)
Triple-negative breast cancer (TNBC) is associated with a worse prognosis and higher mortality than other breast cancers, and intensive effort has been made to develop therapies targeting TNBC. TNBC shows higher expression levels of programmed cell death ligand 1 (PD-L1) than other breast cancer types, which leads to a decrease in the killing effects of CD8+ T cells in the tumor microenvironment. Inhibitors of apoptosis proteins (IAPs) could prevent cell death through suppressing caspase activity. Here, Birinapant, an antagonist of IAPs, was found to promote the tumor infiltration of CD8+ T cells via increasing the secretion of the chemokine CXCL9. In addition, Birinapant could inhibit tumor growth via increasing the secretion of and the sensitivity to TNF-α in a TNBC xenotransplantation mouse model. Consequently, liposomes encapsulating Birinapant and siPD-L1 mediated a form of combination therapy based on two drugs to significantly increase the therapeutic effects toward TNBC.
Keyphrases
  • cell death
  • combination therapy
  • mouse model
  • cell cycle arrest
  • cancer therapy
  • oxidative stress
  • rheumatoid arthritis
  • drug delivery
  • cardiovascular disease
  • type diabetes
  • cell proliferation