Reduced cellular transport and activation of fluoropyrimidine nucleosides and resistance in human lymphocytic cell lines selected for arabinosylcytosine resistance.
暂无分享,去创建一个
[1] P. Yo,et al. Cross-resistance of dideoxycytidine-resistant cell lines to azidothymidine. , 1999, Biochemical pharmacology.
[2] R. Agarwal,et al. Collateral resistance of a dideoxycytidine-resistant cell line to 5-fluoro-2'-deoxyuridine. , 1999, Biochemical and biophysical research communications.
[3] G. Peters,et al. Common resistance mechanisms to deoxynucleoside analogues in variants of the human erythroleukaemic line K562 , 1999, British journal of haematology.
[4] J. Mackey,et al. Nucleoside transporters: molecular biology and implications for therapeutic development. , 1999, Molecular medicine today.
[5] J. Mitsuhashi,et al. Mechanisms for 5-fluorouracil resistance in human colon cancer DLD-1 cells. , 1998, Biological & pharmaceutical bulletin.
[6] G. Peters,et al. Comparison of 5-fluoro-2'-deoxyuridine with 5-fluorouracil and their role in the treatment of colorectal cancer. , 1998, European journal of cancer.
[7] A. Krishan,et al. Flow cytometric analysis of the multiple drug resistance phenotype , 1997, Leukemia.
[8] M. Wientjes,et al. Bladder tissue pharmacokinetics and antitumor effect of intravesical 5-fluorouridine. , 1997, Clinical cancer research : an official journal of the American Association for Cancer Research.
[9] D. Kerr,et al. Hepatic arterial chemotherapy for metastatic colorectal carcinoma. , 1994, British Journal of Cancer.
[10] J. R. Patton. In vitro splicing of pre-messenger RNA with extracts from 5-fluorouridine-treated cells. , 1994, The Biochemical journal.
[11] M. Yin,et al. Isolation and characterization of a human ileocecal carcinoma cell line (HCT-8) subclone resistant to fluorodeoxyuridine. , 1993, Biochemical pharmacology.
[12] Richie Jp. Intravesical chemotherapy. Treatment selection, techniques, and results. , 1992 .
[13] A. Sartorelli,et al. RNA-directed actions of 5-fluorouridine in hemin stimulated K-562 erythroleukemia cells. , 1992, Cancer biochemistry biophysics.
[14] P. Watkins,et al. Rapid and efficient cloning of Alu-PCR products using uracil DNA glycosylase. , 1991, PCR methods and applications.
[15] A. Mian,et al. Thymidine and zidovudine metabolism in chronically zidovudine-exposed cells in vitro. , 1991, Biochemical pharmacology.
[16] B. Oberg,et al. Comparison of the substrate specificities of human thymidine kinase 1 and 2 and deoxycytidine kinase toward antiviral and cytostatic nucleoside analogs. , 1991, Biochemical and biophysical research communications.
[17] L. Johnson,et al. Thymidylate synthase overproduction and gene amplification in fluorodeoxyuridine-resistant human cells. , 1985, Molecular pharmacology.
[18] K. Bhalla,et al. Isolation and Characterization of a Deoxycytidine Kinase-deficient Human Promyelocyte Leukemic Cell Line Highly Resistant to 1-β-D- Arabinofuranosylcytosine , 1984 .
[19] P. Danenberg,et al. Human leukemic cells resistant to 5-fluoro-2'-deoxyuridine contain a thymidylate synthetase with lower affinity for nucleotides. , 1983, The Journal of biological chemistry.
[20] H. Preisler,et al. A pilot study of high-dose 1-beta-D-arabinofuranosylcytosine for acute leukemia and refractory lymphoma: clinical response and pharmacology. , 1982, Cancer research.
[21] J. Wiley,et al. Cytosine arabinoside influx and nucleoside transport sites in acute leukemia. , 1982, The Journal of clinical investigation.
[22] D. Kufe,et al. Correlation of cytotoxicity with incorporation of ara-C into DNA. , 1980, The Journal of biological chemistry.
[23] R. McIvor,et al. Facilitated transport of uracil and 5‐fluorouracil, and permeation of orotic acid into cultured mammalian cells , 1980, Journal of cellular physiology.
[24] P. Danenberg. Thymidylate synthetase - a target enzyme in cancer chemotherapy. , 1977, Biochimica et biophysica acta.
[25] Y. Cheng,et al. Human deoxycytidine kinase. Purification and characterization of the cytoplasmic and mitochondrial isozymes derived from blast cells of acute myelocytic leukemia patients. , 1977, Biochimica et biophysica acta.
[26] D. Wilkinson,et al. Metabolism of 5-fluorouracil in sensitive and resistant Novikoff hepatoma cells. , 1977, The Journal of biological chemistry.
[27] R. Momparler,et al. A model for the chemotherapy of acute leukemia with 1-beta-D-arabinofuranosylcytosine. , 1974, Cancer research.
[28] C. Heidelberger,et al. Thymidylate synthetase: mechanism of inhibition by 5-fluoro-2'-deoxyuridylate. , 1972, Biochemical and biophysical research communications.
[29] J. Furth,et al. Inhibition of Mammalian DNA Polymerase by the 5′-Triphosphate of 1-β-d-Arabinofuranosylcytosine and the 5′-Triphosphate of 9-β-d-Arabinofuranosyladenine , 1968 .
[30] H. Skipper,et al. Experimental evaluation of potential anticancer agents. XXI. Scheduling of arabinosylcytosine to take advantage of its S-phase specificity against leukemia cells. , 1967, Cancer chemotherapy reports.
[31] T. Tong,et al. Cancer statistics, 1994 , 1994, CA: a cancer journal for clinicians.
[32] Y. Cheng,et al. Metabolism and mechanism of action of 5-fluorouracil. , 1990, Pharmacology & therapeutics.
[33] H. Tsutani,et al. Transport and intracellular metabolism of fluorinated pyrimidines in cultured cell lines. , 1989, Advances in experimental medicine and biology.
[34] Jackson Rc,et al. Membrane transport alterations as a mechanism of resistance to anticancer agents. , 1986 .