We have developed an in vitro model to study mechanisms by which ovarian tumor cells that over-express the HER-2/ neu proto-oncogene escape recognition by T CD8 1 . Nine tumorspecific, HLA A2-restricted T CD8 1 clones were isolated from 2 ovarian tumor-specific T CD8 1 lines derived from tumorinfilt
Affibody-displaying bionanocapsules for specific drug delivery to HER2-expressing cancer cells
โ Scribed by Takuya Shishido; Hiroaki Mieda; Sang Youn Hwang; Yuya Nishimura; Tsutomu Tanaka; Chiaki Ogino; Hideki Fukuda; Akihiko Kondo
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 661 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-894X
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โฆ Synopsis
A novel HER2-targeted carrier was developed using bionanocapsules (BNCs). Bionanocapsules (BNCs) are 100-nm hollow nanoparticles composed of the L-protein of hepatitis B virus surface antigen. An affibody of HER2 was genetically displayed on the BNC surface (Z(HER2)-BNC). For the investigation of binding affinity, Z(HER2)-BNC was incubated with the cancer cell lines SK-BR-3 (HER2 positive), and MDA-MB-231 (HER2 negative). For analysis of HER2 targeting specificity, Z(HER2)-BNC or Z(WT)-BNC (without affibody) was incubated with both SK-BR-3 and MDA-MB-231 cells by time lapse and concentration. For the delivery of encapsulated molecules (calcein), fluorescence of Z(HER2)-BNC mixed with liposomes was also compared with that of Z(WT)-BNC and nude liposomes by incubation with SK-BR-3 cells. As a result, Z(HER2)-BNC-liposome complex demonstrated the delivery to HER2-expressing cells (SK-BR-3) with a high degree of specificity. This indicates that genetically engineered BNCs are promising carrier for cancer treatment.
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