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Development of a Novel Humanized Monoclonal Antibody to Secreted Frizzled-Related Protein-2 That Inhibits Triple-Negative Breast Cancer and Angiosarcoma Growth In Vivo
- Source :
- Ann Surg Oncol
- Publication Year :
- 2019
-
Abstract
- We previously reported that secreted frizzled-related protein-2 (SFRP2) is expressed in a variety of tumors, including sarcoma and breast carcinoma, and stimulates angiogenesis and inhibits tumor apoptosis. Therefore, we hypothesized that a humanized SFRP2 monoclonal antibody (hSFRP2 mAb) would inhibit tumor growth. The lead hSFRP2 antibody was tested against a cohort of 22 healthy donors using a time course T-cell assay to determine the relative risk of immunogenicity. To determine hSFRP2 mAb efficacy, nude mice were subcutaneously injected with SVR angiosarcoma cells and treated with hSFRP2 mAb 4 mg/kg intravenously every 3 days for 3 weeks. We then injected Hs578T triple-negative breast cells into the mammary fat pad of nude mice and treated for 40 days. Control mice received an immunoglobulin (Ig) G1 control. The SVR and Hs578T tumors were then stained using a TUNEL assay to detect apoptosis. Immunogenicity testing of hSFRP2 mAb did not induce proliferative responses using a simulation index (SI) ≥ 2.0 (p
- Subjects :
- medicine.drug_class
Angiogenesis
Hemangiosarcoma
Mice, Nude
Apoptosis
Triple Negative Breast Neoplasms
Monoclonal antibody
Antibodies, Monoclonal, Humanized
Article
03 medical and health sciences
Mice
0302 clinical medicine
Breast cancer
medicine
Tumor Cells, Cultured
Animals
Humans
Triple-negative breast cancer
Cell Proliferation
biology
Neovascularization, Pathologic
business.industry
Immunogenicity
Membrane Proteins
medicine.disease
Xenograft Model Antitumor Assays
Oncology
030220 oncology & carcinogenesis
Monoclonal
biology.protein
Cancer research
030211 gastroenterology & hepatology
Surgery
Female
Sarcoma
Antibody
business
Subjects
Details
- ISSN :
- 15344681
- Volume :
- 26
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Annals of surgical oncology
- Accession number :
- edsair.doi.dedup.....d3dcfa43bd679d5051ae76d35780fe9f