Immunogenic Treatment of Metastatic Breast Cancer Using Targeted Carbon Nanotube Mediated Photothermal Therapy in

Gabriela N F Faria1, Clement G Karch1, Sampurna Chakraborty1

  • 1School of Sustainable Chemical, Biological, and Materials Engineering (G.N.F.F., R.P.S., D.R., R.G.H.), School of Biomedical Engineering (C.G.K., S.C., A.W., A.A.), and Samuel Roberts Noble Microscopy Laboratory and School of Biological Sciences (T.G.), University of Oklahoma, Norman, Oklahoma; CHASM Advanced Materials, Inc, Norman, Oklahoma (S.L., R.P.S.); Department of Microbiology and Immunology, Universidad Nacional de San Agustin, Arequipa, Peru (J.A.B.); and Stephenson Cancer Center, Oklahoma City, Oklahoma (R.G.H.).

Insights

Novel breast cancer treatment combines targeted photothermal therapy with immune checkpoint inhibition. This approach, using SWCNT-ANXA5 conjugates, significantly increased survival rates in mice, demonstrating a promising new strategy for advanced breast cancer.

Area of Science:

  • Biomedical Engineering
  • Oncology
  • Nanotechnology

Background:

  • Advanced breast cancer lacks safe and effective treatments, necessitating novel therapeutic strategies.
  • Annexin A5 (ANXA5) targets externalized phosphatidylserine on tumor cells and vasculature.
  • Single-walled carbon nanotubes (SWCNTs) offer potential as photosensitizers for photothermal therapy (PTT).

Purpose of the Study:

  • To develop a targeted photosensitizer for PTT of solid tumors using SWCNT-ANXA5 conjugates.
  • To evaluate the synergistic effects of SWCNT-ANXA5-mediated PTT combined with checkpoint inhibition.
  • To assess the in vivo efficacy and safety of this combined treatment strategy in a breast cancer model.

Main Methods:

  • Functionalization of SWCNTs with ANXA5 to create SWCNT-ANXA5 conjugates.
  • In vitro evaluation of conjugate-mediated cell ablation.
  • In vivo testing in an orthotopic EMT6 breast tumor model in mice, utilizing intratumoral injection and PTT at 45°C, combined with anti-programmed cell death protein-1 (anti-PD-1) therapy.

Main Results:

  • SWCNT-ANXA5 conjugates demonstrated targeted and dose-dependent in vitro cell death.
  • Intratumoral injection of SWCNT-ANXA5 prevented accumulation in major clearance organs.
  • Combined PTT and anti-PD-1 therapy resulted in 80% survival at 100 days in mice, with evidence of systemic immune activation and potential abscopal effect.

Conclusions:

  • SWCNT-ANXA5-mediated PTT, when administered intratumorally and combined with checkpoint inhibition, offers a highly effective treatment for aggressive breast cancer.
  • This strategy achieves significant survival benefits at a relatively low PTT temperature (45°C) and avoids nanotube accumulation in clearance organs.
  • The observed systemic anticancer immune response suggests a promising therapeutic approach for advanced solid tumors.

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