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引用本文的文献

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In vitro and in vivo cytotoxicity of alkyl lysophospholipid ET-18-OCH3 and thioether lipid BM 41.440.烷基溶血磷脂ET-18-OCH3和硫醚脂质BM 41.440的体外和体内细胞毒性
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2
Phase I trial of the thioether phospholipid analogue BM 41.440 in cancer patients.
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本文引用的文献

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Endoscopic diagnosis of chemically induced autochthonous colonic tumors in rats.
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Studies on various parameters influencing leukemic cell destruction by alkyl-lysophospholipids.关于影响烷基溶血磷脂对白血病细胞破坏作用的各种参数的研究。
Anticancer Res. 1982 Jan-Apr;2(1-2):95-100.
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Anti-tumor action of alkyl-lysophospholipids (Review).烷基溶血磷脂的抗肿瘤作用(综述)
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Survival and response to chemotherapy for advanced colorectal adenocarcinoma: an Eastern Cooperative Oncology Group report.晚期结直肠腺癌的生存情况及对化疗的反应:东部肿瘤协作组报告
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Chemotherapeutic studies on N-nitrosoacetoxymethyl-methylamine-and 1,2-dimethylhydrazine-induced colonic tumors in rats: monotherapy with 5-fluorouracil, ftorafur, CGP 6809, and CGP 15'720A.N-亚硝基乙酰氧基甲基甲胺和1,2-二甲基肼诱导的大鼠结肠肿瘤的化疗研究:5-氟尿嘧啶、替加氟、CGP 6809和CGP 15720A单药治疗
J Cancer Res Clin Oncol. 1982;104(1-2):115-31. doi: 10.1007/BF00402060.
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Cytotoxicity of thioether-lysophospholipids in leukemias and tumors of human origin.
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Chemotherapy in alimentary tract malignomas.消化道恶性肿瘤的化疗
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Quantitative comparison of toxicity of anticancer agents in mouse, rat, hamster, dog, monkey, and man.抗癌药物在小鼠、大鼠、仓鼠、狗、猴和人类中毒性的定量比较。
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Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples.需要对每位患者进行长期观察的随机临床试验的设计与分析。II. 分析与示例。
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Design and analysis of randomized clinical trials requiring prolonged observation of each patient. I. Introduction and design.需要对每位患者进行长期观察的随机临床试验的设计与分析。I. 引言与设计。
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在单药化疗和联合化疗中使用硫醚溶血磷脂衍生物治疗自发性大鼠结肠腺癌

Treatment of autochthonous rat colonic adenocarcinomas with a thioether-lysophospholipid derivative in mono- and combination chemotherapy.

作者信息

Heim M E, Swoboda M, Pahlke W, Edler L, Bicker U

出版信息

J Cancer Res Clin Oncol. 1984;108(3):316-20. doi: 10.1007/BF00390465.

DOI:10.1007/BF00390465
PMID:6549010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12252807/
Abstract

In 361 Sprague-Dawley rats autochthonous colorectal carcinomas were induced by intrarectal application of the carcinogen AMMN. Tumor-bearing animals were treated with a synthetic thioether-lysophospholipid (TLP) derivative and in combination chemotherapy with 5-fluorouracil (5-FU) and carmustine (BCNU). There was no difference in the survival time of treated and untreated animals. The median large-bowel tumor weight was significantly lower in the TLP/5-FU and TLP/5-FU/BCNU combination therapy groups than in the control groups. Transient hepatotoxicity was observed in the high-dosage (50 mg/kg body weight twice weekly) TLP group. This study confirmed the relative resistance of AMMN-induced colorectal carcinomas to antineoplastic treatment.

摘要

在361只Sprague-Dawley大鼠中,通过直肠内施用致癌物AMMN诱导原位结直肠癌。对荷瘤动物用合成硫醚-溶血磷脂(TLP)衍生物进行治疗,并与5-氟尿嘧啶(5-FU)和卡莫司汀(BCNU)联合化疗。治疗组和未治疗组动物的生存时间没有差异。TLP/5-FU和TLP/5-FU/BCNU联合治疗组的大肠肿瘤中位数重量显著低于对照组。在高剂量(每周两次,50mg/kg体重)TLP组中观察到短暂的肝毒性。本研究证实了AMMN诱导的结直肠癌对抗肿瘤治疗具有相对抗性。