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Correlations between cytotoxicity, biochemical effects, drug levels, and therapeutic effectiveness of daunomycin and adriamycin on Sarcoma 180 ascites in mice.

作者信息

Silvestrini R, Lenaz L, Di Fronzo G, Sanfilippo O

出版信息

Cancer Res. 1973 Nov;33(11):2954-8.

PMID:4748447
Abstract
摘要

相似文献

1
Correlations between cytotoxicity, biochemical effects, drug levels, and therapeutic effectiveness of daunomycin and adriamycin on Sarcoma 180 ascites in mice.
Cancer Res. 1973 Nov;33(11):2954-8.
2
Comparative biochemical studies of adriamycin and daunomycin in leukemic cells.
Cancer Res. 1972 Mar;32(3):511-5.
3
Metabolic effects of some tumor-inhibitory pyridine carboxaldehyde thiosemicarbazones.某些具有肿瘤抑制作用的吡啶羧醛缩氨基硫脲的代谢效应
Cancer Res. 1971 Mar;31(3):228-34.
4
Evidence for the lack of relationship between inhibition of nucleic acid synthesis and cytotoxicity of adriamycin.阿霉素抑制核酸合成与细胞毒性之间缺乏相关性的证据。
Cancer Biochem Biophys. 1983;6(3):137-42.
5
[Correlation between fixation of daunomycin-H 3 and antimitotic and antimetabolic activity in ascitic sarcoma 180].[柔红霉素-H³的结合与腹水型肉瘤180的抗有丝分裂及抗代谢活性之间的相关性]
Tumori. 1971 Mar-Apr;57(2):67-74. doi: 10.1177/030089167105700201.
6
Effect of an epipodophyllotoxin derivative (VP 16-213) on macromolecular synthesis and mitosis in mastocytoma cells in vitro.一种鬼臼毒素衍生物（VP 16 - 213）对体外肥大细胞瘤细胞中大分子合成及有丝分裂的影响。
Cancer Res. 1974 Aug;34(8):1788-93.
7
Increased relative effectiveness of doxorubicin against slowly proliferating sarcoma 180 cells after prolonged drug exposure.延长药物暴露时间后，阿霉素对缓慢增殖的肉瘤180细胞的相对有效性增加。
Cancer Treat Rep. 1982 May;66(5):1159-68.
8
Biochemical effects of the Vinca alkaloids. IV. Studies with vinleurosine.
Biochem Pharmacol. 1969 Jan;18(1):227-32. doi: 10.1016/0006-2952(69)90027-6.
9
Experimentally developed cellular resistance to daunomycin. Resistance mechanisms, the daunomycin-pump and cross resistance to adriamycin, vincristine and vinblastine.实验诱导的细胞对柔红霉素的耐药性。耐药机制、柔红霉素泵以及对阿霉素、长春新碱和长春花碱的交叉耐药性。
Acta Pathol Microbiol Scand Suppl. 1976(256 Suppl):3-80.
10
Some determinants of the therapeutic efficacy of actinomycin D (NSC-3053), adriamycin (NSC-123127), and daunorubicin (NSC-83142).
Cancer Chemother Rep. 1974 Jan-Feb;58(1):55-62.

引用本文的文献

1
Is the drug-responsive NADH oxidase of the cancer cell plasma membrane a molecular target for adriamycin?癌细胞质膜上对药物敏感的NADH氧化酶是阿霉素的分子靶点吗？
J Bioenerg Biomembr. 1997 Jun;29(3):269-80. doi: 10.1023/a:1022414228013.
2
Inhibition of plasma membrane NADH dehydrogenase by adriamycin and related anthracycline antibiotics.阿霉素及相关蒽环类抗生素对质膜NADH脱氢酶的抑制作用。
J Bioenerg Biomembr. 1984 Jun;16(3):209-21. doi: 10.1007/BF00751050.
3
Comparison of the cellular pharmacology of doxorubicin in resistant and sensitive models of pancreatic cancer.
阿霉素在胰腺癌耐药和敏感模型中的细胞药理学比较。
Cancer Chemother Pharmacol. 1985;14(2):132-4. doi: 10.1007/BF00434351.
4
[On the problem of praetherapeutic sensitivity testing of human tumours based on incorporation studies of nucleic acid precursors in vitro (author's transl)].[关于基于体外核酸前体掺入研究的人类肿瘤治疗前敏感性测试问题（作者译）]
Klin Wochenschr. 1977 Dec 1;55(23):1127-36. doi: 10.1007/BF01478050.