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Wistar Furth大鼠急性髓性白血病的化疗缓解:一种人类急性髓系白血病模型

Chemotherapeutic remissions in Wistar Furth rat acute myelogenous leukemia: a model for human AML.

作者信息

Greenberger J S, Bocaccino C A, Szot S J, Moloney W C

出版信息

Acta Haematol. 1977 Mar;57(4):233-41. doi: 10.1159/000207886.

Abstract

Acute myelogenous leukemia (AML) of the inbred Wistar/Furth (W/Fu) rat is pathophysiologically similar to human AML. Subcutaneous transplantation of 1.0 X 10(6) cells of a clonal tissue culture line of W/Fu AML into 6- to 8-week-old rats produced local myeloblastomas in 8--10 days which progressed to infiltration of regional nodes, replacement of greater than 90% of the bone marrow, ascites, and fatal peripheral blood leukemia with concomitant hyperlysozymemia. Single doses of adriamycin, daunomycin, actinomycin, cytosine arabinoside, or Cytoxan in rats with 1.0 cm myeloblastomas produced complete tumor regression while bu-sulfan, vinblastine, vincristine, dexamethasone, and Methotrexate was relatively ineffective. Responses were associated with delay in progression to peripheral blood leukemia and prolonged survival. Similar results were obtained following treatment of rats with already disseminated leukemia. The demonstration of response to drugs known active against human AML indicates that the W/Fu AML should be a valuable model for rapid evaluation of new chemotherapeutic agents for clinical use.

摘要

近交系Wistar/Furth(W/Fu)大鼠的急性髓性白血病(AML)在病理生理学上与人类AML相似。将1.0×10⁶个W/Fu AML克隆组织培养系细胞皮下移植到6至8周龄大鼠体内,8至10天内产生局部成髓细胞瘤,随后进展为区域淋巴结浸润、骨髓替代率超过90%、腹水以及伴有高溶菌酶血症的致命外周血白血病。单剂量阿霉素、柔红霉素、放线菌素、阿糖胞苷或环磷酰胺可使患有1.0厘米成髓细胞瘤的大鼠肿瘤完全消退,而白消安、长春碱、长春新碱、地塞米松和甲氨蝶呤相对无效。这些反应与外周血白血病进展延迟和生存期延长相关。对已发生白血病的大鼠进行治疗后也获得了类似结果。对已知对人类AML有效的药物产生反应的证明表明,W/Fu AML应是快速评估用于临床的新型化疗药物的有价值模型。

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