Role of E2F-1 in chemosensitivity
| Autor: | D, Banerjee, B, Schnieders, J Z, Fu, D, Adhikari, S C, Zhao, J R, Bertino |
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| Rok vydání: | 1998 |
| Předmět: |
Antimetabolites
Antineoplastic Paclitaxel Cell Survival Fibrosarcoma Antineoplastic Agents Cell Cycle Proteins Irinotecan Transfection Culture Media Serum-Free Tumor Cells Cultured Humans Cloning Molecular Etoposide Cell Cycle Antineoplastic Agents Phytogenic Recombinant Proteins E2F Transcription Factors DNA-Binding Proteins Tetrahydrofolate Dehydrogenase Doxorubicin Camptothecin Carrier Proteins Transcription Factor DP1 Cell Division E2F1 Transcription Factor Retinoblastoma-Binding Protein 1 Transcription Factors |
| Zdroj: | Cancer research. 58(19) |
| ISSN: | 0008-5472 |
| Popis: | The E2F family of transcription factors, in partnership with DP proteins, is thought to regulate transcription of genes that encode protein products that are required for DNA synthesis, which include important cancer chemotherapeutic targets such as thymidylate synthase and dihydrofolate reductase. This study was conducted to investigate the effects of overexpression of human E2F-1 cDNA on chemosensitivity in a human fibrosarcoma cell line, HT-1080. The E2F-1-overexpressing HT-1080 cells had a shorter doubling time both in vitro and in vivo. Associated with an up-regulation of TS, E2F-1-transfected cells were more resistant to 5-fluorouracil than were untransfected cells. These E2F-1 transfectants, although resistant to fluoropyrimidines and serum deprivation, were more sensitive to etoposide, doxorubicin, and SN38 (the active metabolite of irinotecan) but not to Taxol. |
| Databáze: | OpenAIRE |
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