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Near-Infrared Photoimmunotherapy Using a Small Protein Mimetic for HER2-Overexpressing Breast Cancer.
Yamaguchi, Haruka; Pantarat, Namfon; Suzuki, Takamasa; Evdokiou, Andreas.
Affiliation
  • Yamaguchi H; Discipline of Surgery, Breast Cancer Research Unit, Basil Hetzel Institute, University of Adelaide, Adelaide, SA, 5011, Australia.
  • Pantarat N; Department of Life Science Dentistry, The Nippon Dental University, Niigata, 951-8580, Japan.
  • Suzuki T; Department of Oral and Maxillofacial Radiology, The Nippon Dental University School of Life Dentistry at Niigata, Niigata, 951-8580, Japan.
  • Evdokiou A; Discipline of Surgery, Breast Cancer Research Unit, Basil Hetzel Institute, University of Adelaide, Adelaide, SA, 5011, Australia.
Int J Mol Sci ; 20(23)2019 Nov 20.
Article in En | MEDLINE | ID: mdl-31757056
ABSTRACT
Near-infrared photoimmunotherapy (NIR-PIT) is a new and promising cancer therapy based on a monoclonal antibody conjugated to a photosensitizer which is activated by near-infrared light irradiation, causing cell death. We investigated NIR-PIT using a small protein mimetic (6-7 kDa), Affibody molecules, instead of a monoclonal antibody for HER2-overexpressing cancer. Because of its small size, the Affibody has rapid clearance, high imaging contrast, and good tumor penetration. Due to the small size of the Affibodies, which can cross the blood-brain barrier, NIR-PIT using Affibodies has the potential to extend the target cancer of NIR-PIT, including brain metastases. In vitro, NIR-PIT using HER2 Affibody-IR700Dye conjugates induced the selective destruction of HER2-overexpressing breast cancer cells without damage to control cells having low level expression of HER2. HER2-overexpressing cancer cells showed necrotic cell death and their viability maintained at low levels, even 5 days after NIR-PIT. In contrast, treatment with high concentration of HER2 Affibody-IR700Dye conjugate alone or irradiation with high dose of NIR light alone was without effect on cell viability. Affibody and IR700Dye are currently used clinically, and therefore, we would expect the current formulation to be safely and quickly transitioned into clinical trials.
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Full text: 1 Database: MEDLINE Main subject: Peptide Fragments / Phototherapy / Breast Neoplasms / Receptor, ErbB-2 / Immunotherapy / Antibodies, Monoclonal / Antineoplastic Agents Language: En Journal: Int J Mol Sci Year: 2019 Type: Article Affiliation country: Australia

Full text: 1 Database: MEDLINE Main subject: Peptide Fragments / Phototherapy / Breast Neoplasms / Receptor, ErbB-2 / Immunotherapy / Antibodies, Monoclonal / Antineoplastic Agents Language: En Journal: Int J Mol Sci Year: 2019 Type: Article Affiliation country: Australia