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TRAMP-C2可移植前列腺癌动物模型的建立及初步应用 被引量:2

Establishment and application of transplantable TRAMP-C2 prostate cancer mice model
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摘要 目的建立一个可移植前列腺癌动物模型,并用于评价药物的抗肿瘤作用。方法将转基因小鼠前列腺癌细胞株TRAMP-C2接种入C57BL/6N小鼠,体内传代至其生物学特性趋于稳定,观察环磷酰胺(CTX)、中药紫龙金和自拟中药方对模型肿瘤的抑制作用。结果TRAMP—C2接种入C57BL/6N小鼠后,肿瘤开始生长,体内传代4代后基本稳定,皮下接种约1×10^7的细胞,经4周肿瘤可达N2-3g;CTX、紫龙金和自拟中药方对模型肿瘤的生长抑制率分别为83.23%、29.58%和36.03%。结论TRAMP—C2可移植前列腺癌小鼠模型是一个新的动物模型,并可作为抗前列腺癌药物研究之用。 Objective To establish an implantable animal model of prostate cancer, and to app!y it to evaluate the anti-tumor activity of medicine. Methods Transgenic adenocarcinoma mouse prostate cell (TRAMP-C2) suspensions were implanted to C57BL/6N mice subcutaneously at oxter. TRAMP-C2 was went down to the future generates in mice until the biological features were stable. The anti-cancer activity of cyclophosphamide (CTX), TCM recipe Zilongjin and TCM complex prescription were tested on this mice model. Results The biological features were stable after four generations. The weight of tumor reached 2-3g four weeks after hypodermic inoculation of 1 ×10^7 cells. The growth inhibiting ratios of tumor were 83. 23% 29. 58% and 36. 03% for CTX, Zilongiin and TCM complex prescription, respectively. Conclusion The establishment of TRAMP-C2 implantable mice model provided a new model for the study of prostate cancer medicine treatment.
出处 《北京中医药大学学报》 CAS CSCD 北大核心 2008年第3期189-191,195,I0002,共5页 Journal of Beijing University of Traditional Chinese Medicine
关键词 前列腺癌 动物模型 TRAMP—C2 中药 小鼠 prostate cancer animal model transgenic adenocarcinoma mouse prostate cell (TRAMP-C2) Chinese materia medica mice
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  • 1GREENIZE RT, MURRAY T, BOLDEN S, et al. Cancer statistics 2000[J]. CA-Cancer J Clin, 2000, 50:7 -33.
  • 2FOSTER BA, GINGRICH JR, KWON ED, et al. Characterization of prostatic epithelial cell lines derived from transgenic adenocarcinoma of the mouse prostate (TRAMP) model [ J]. Cancer Research, 1997, 57:3325 - 3330.
  • 3GREENBERG NM, DEMAYO F, FINEGOLD M, et al. Prostate cancer in a transgenic mouse [ J ]. Proc. Natl. Acad. Sci. USA, 1995, 92:3439-3443.

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