Selective death of human breast cancer cells by lytic immunoliposomes: Correlation with their HER2 expression level

被引:50
作者
Barrajon-Catalan, Enrique [1 ]
Menendez-Gutierrez, Maria P. [1 ]
Falco, Alberto [1 ]
Carrato, Alfredo [2 ]
Saceda, Miguel [2 ]
Micol, Vicente [1 ]
机构
[1] Miguel Hernandez Univ, Inst Mol & Cell Biol, IBMC, E-03202 Alicante, Spain
[2] Elche Univ Hosp, Biomed Res Fdn FIBEIx, Alicante 03203, Spain
关键词
Trastuzumab; Immunoliposomes; Melittin; Cell lysis; HER2; Anticancer therapy; Breast cancer cells; STERICALLY STABILIZED LIPOSOMES; IN-VITRO; ANTI-HER2; IMMUNOLIPOSOMES; ANTIMICROBIAL PEPTIDES; TUMOR-CELLS; MONOCLONAL-ANTIBODY; DRUG-DELIVERY; BEE VENOM; MELITTIN; VIVO;
D O I
10.1016/j.canlet.2009.09.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trastuzumab (Herceptin (TM)) targets the human epidermal growth factor receptor 2 (HER2), which is overexpressed in 20-30% of breast and ovarian cancers carrying a bad prognosis. Our purpose was to target HER2-overexpressing human breast cancer cells with pegylated immunoliposomes bearing trastuzumab and containing melittin, which has recently shown anticancer properties. Using a panel of human breast cancer cells with different HER2 expression levels, these immunoliposomes decreased cancer cells viability in a dose-response manner and in correlation to their level of HER2 expression. Specific binding of the immunoliposomes to SKBr3 breast cancer cells was shown by ImageStream-based analysis. The morphological changes observed in the treated cells suggested a cytolytic process. This preclinical approach may suppose an effective strategy for the treatment of HER2-overexpressing tumors, and can support the development of an early phases I-II clinical trial. Trastuzumab resistant breast cancer cells (JIMT-1), can also be targeted using this approach. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:192 / 203
页数:12
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