Cellular FLICE-inhibitory protein regulates chemotherapy-induced apoptosis in breast cancer cells
| Autor: | Leeona Galligan, Patrick G. Johnston, M. Thomas, Hidekazu Sakai, Daniel B. Longley, Timothy R. Wilson, Katherine Rogers, Wendy L. Allen |
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| Rok vydání: | 2007 |
| Předmět: |
Cancer Research
Small interfering RNA Blotting Western CASP8 and FADD-Like Apoptosis Regulating Protein Down-Regulation Antineoplastic Agents Breast Neoplasms Biology Irinotecan Interferon-gamma Breast cancer Cell Line Tumor medicine Gene silencing Humans Doxorubicin Gene Silencing Transcription factor Etoposide Regulation of gene expression Caspase 8 Dose-Response Relationship Drug medicine.disease Gene Expression Regulation Neoplastic Oncology Apoptosis STAT protein Cancer research Camptothecin Mitoxantrone medicine.drug |
| Zdroj: | Molecular cancer therapeutics. 6(5) |
| ISSN: | 1535-7163 |
| Popis: | Combination treatment regimens that include topoisomerase-II–targeted drugs, such as doxorubicin, are widely used in the treatment of breast cancer. Previously, we showed that IFN-γ and doxorubicin cotreatment synergistically induced apoptosis in MDA435 breast cancer cells in a signal transducer and activator of transcription 1–dependent manner. In this study, we found that this synergy was caspase-8 dependent. In addition, we found that IFN-γ down-regulated the expression of the caspase-8 inhibitor cellular FLICE-inhibitory protein (c-FLIP). Furthermore, IFN-γ down-regulated c-FLIP in a manner that was dependent on the transcription factors signal transducer and activator of transcription 1 and IFN regulatory factor-1. However, IFN-γ had no effect on c-FLIP mRNA levels, indicating that c-FLIP was down-regulated at a posttranscriptional level following IFN-γ treatment. Characterization of the functional significance of c-FLIP modulation by small interfering RNA gene silencing and stable overexpression studies revealed it to be a key regulator of IFN-γ– and doxorubicin-induced apoptosis in MDA435 cells. Analysis of a panel of breast cancer cell lines indicated that c-FLIP was an important general determinant of doxorubicin- and IFN-γ–induced apoptosis in breast cancer cells. Furthermore, c-FLIP gene silencing sensitized MDA435 cells to other chemotherapies, including etoposide, mitoxantrone, and SN-38. These results suggest that c-FLIP plays a pivotal role in modulating drug-induced apoptosis in breast cancer cells. [Mol Cancer Ther 2007;6(5):1544–51] |
| Databáze: | OpenAIRE |
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