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The Cell Cycle Regulatory Effects of High Dose 5-fluorouracil on Breast Cancer Cell Line  

Jang, Joung Soon (Department of Internal Medicine and Gyeong Sang Institute of Health Science, Gyeong Sang National University College of Medicine)
Yang, Jung Ill (Department of Internal Medicine and Gyeong Sang Institute of Health Science, Gyeong Sang National University College of Medicine)
Chang, Seho (Department of Internal Medicine and Gyeong Sang Institute of Health Science, Gyeong Sang National University College of Medicine)
Lee, Won Sup (Department of Internal Medicine and Gyeong Sang Institute of Health Science, Gyeong Sang National University College of Medicine)
Lee, Jong Seok (Department of Internal Medicine and Gyeong Sang Institute of Health Science, Gyeong Sang National University College of Medicine)
Ahn, Myung-Ju (Department of Internal Medicine, Hanyang University College of Medicine)
Park, Byung-Kiu (National Cancer Center)
Publication Information
IMMUNE NETWORK / v.2, no.1, 2002 , pp. 60-64 More about this Journal
Abstract
Background: Chemotherapy with 5-fluorouracil (5-FU) has been one of the mainstay in breast cancer treatment. The effects of high dose 5-FU on cell cycle regulation were studied in breast caner cells. Methods: A breast cancer cell line MCF-7 was used. Protein expressions of G1/S cyclins, $p21^{Waf1/Cip1}$, cdk2, E2F1 and retinoblastoma were tested by western blot analysis. Immunoprecipitation and immune complex kinase assay were done for the assessment of E2F1/RB interacton and the activity of cdk2 respectively. Results: $p21^{Waf1/Cip1}$ expression was barely detectable in control cells. With addition of 5-FU level of $p21^{Waf1/Cip1}$ were induced and cyclin D3 level was decreased as cell growth decreases. In accordance with increased expression of $p21^{Waf1/Cip1}$, cyclin E-associated cdk2 kinase activity was reduced. Retinoblastoma protein (RB) became dephosphorylated and E2F-1 binding activity with RB was increased. Conclusion: In this situation of high concentration of 5-FU breast cancer cells tend to be G1/S cell cycle arrested. Overexpression of $p21^{Waf1/Cip1}$ and dephosphorylation of RB may mediate the effectss of 5-FU by inhibiting E2F-1 activity, which contributes to G1/S cell cycle arrest. These results could be an indicating landmark for further study of high dose chemotherapy with 5-FU.
Keywords
5-FU; breast cancer; cell cycle regulation;
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