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J Cell Biochem ; 99(3): 665-70, 2006 Oct 15.
Article in English | MEDLINE | ID: mdl-16795032

ABSTRACT

We hypothesized that estrogen receptor (ER) in hormone-sensitive breast cancer cells could be targeted for selective photodynamic killing of tumor cell with antiestrogen-porphyrin conjugates by combining the over-expression of ER in hormone-sensitive breast cancer cells and tumor-retention property of porphyrin photosensitizers. In this study we describe that a tamoxifen (TAM)-pyropheophorbide conjugate that specifically binds to ER alpha, caused selective cell-kill in MCF-7 breast cancer cells upon light exposure. Therefore, it is a potential candidate for ER-targeted photodynamic therapy of cancers (PDT) of tissues and organs that respond to estrogens/antiestrogens.


Subject(s)
Antineoplastic Agents, Hormonal , Breast Neoplasms , Cell Line, Tumor/drug effects , Chlorophyll/analogs & derivatives , Photochemotherapy/methods , Porphyrins/pharmacology , Porphyrins/therapeutic use , Tamoxifen/analogs & derivatives , Antineoplastic Agents, Hormonal/chemistry , Antineoplastic Agents, Hormonal/pharmacology , Antineoplastic Agents, Hormonal/therapeutic use , Breast Neoplasms/drug therapy , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Cell Survival , Chlorophyll/chemistry , Chlorophyll/pharmacology , Chlorophyll/therapeutic use , Estrogen Receptor alpha/metabolism , Female , Humans , Molecular Structure , Porphyrins/chemistry , Selective Estrogen Receptor Modulators/chemistry , Selective Estrogen Receptor Modulators/pharmacology , Selective Estrogen Receptor Modulators/therapeutic use , Tamoxifen/chemistry , Tamoxifen/pharmacology , Tamoxifen/therapeutic use
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