Enhancement of doxorubicin anti-cancer activity by vascular targeting using IsoDGR/cytokine-coated nanogold

Background: Gold nanospheres tagged with peptides containing isoDGR (isoAsp-Gly-Arg), an alpha v beta 3 integrin binding motif, represent efficient carriers for delivering pro-inflammatory cytokines to the tumor vasculature. We prepared bi- or trifunctional nanoparticles bearing tumor necrosis factor-alpha (TNF) and/or interleukin-12 (IL12) plus a peptide containing isoDGR, and we tested their anti-cancer effects, alone or in combination with doxorubicin, in tumor-bearing mice. Results: In vitro biochemical studies showed that both nanodrugs were monodispersed and functional in terms of binding to TNF and IL12 receptors and to alpha v beta 3. In vivo studies performed in a murine model of fibrosarcoma showed that low doses of bifunctional nanoparticles bearing isoDGR and TNF (corresponding to few nanoparticles per cell) delayed tumor growth and increased the efficacy of doxorubicin without worsening its toxicity. Similar effects were obtained using trifunctional nanoparticles loaded with isoDGR,TNF and IL12. Mechanistic studies showed that nanoparticles bearing isoDGR and TNF could increase doxorubicin penetration in tumors a few hours after injection and caused vascular damage at later time points. Conclusion: IsoDGR-coated gold nanospheres can be exploited as a versatile platform for single- or multi-cytokine delivery to cells of the tumor vasculature. Extremely low doses of isoDGR-coated nanodrugs functionalized with TNF or TNF plus IL12 can enhance doxorubicin anti-tumor activity.

Automated summary

Gold nanospheres tagged with isoDGR peptides can efficiently deliver pro-inflammatory cytokines to tumor vasculature. Bifunctional or trifunctional nanoparticles loaded with TNF and/or IL12, along with isoDGR peptides, show anti-cancer effects in a mouse model of fibrosarcoma by delaying tumor growth and enhancing doxorubicin efficacy without increasing toxicity. Mechanistic studies suggest that these nanoparticles can improve doxorubicin penetration in tumors and cause vascular damage.