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转基因厌氧菌对鼠黑色素瘤的靶向性研究 被引量:1

The research on tumor-targeting of transgenic anaerobic bacterium to melanoma in mice
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摘要 目的探讨转基因婴儿双歧杆菌对小鼠黑色素瘤的靶向性。方法经小鼠尾静脉注射转基因婴儿双歧杆菌,通过放射性体内参入示踪分析、组织厌氧培养及组织切片方法,观察转基因厌氧菌对黑色素瘤组织的靶向性。结果肿瘤组织的放射性强度逐渐增强,而正常组织放射性强度逐渐减弱;组织厌氧培养可见转基因厌氧菌在瘤组织内集聚增殖,组织切片可见瘤组织中有大量的革兰氏染色阳性的条杆状蓝色深染区域,而正常组织则无。结论婴儿双歧杆菌对小鼠黑色素瘤组织具有良好的靶向性,可将携带的基因靶向转运至实体瘤局部。 Objective To evaluate tumor-targeting of transgenic bifidobacterium infants to melanoma in mice. Methods After bolus administration of transgenic bifidobacterium infantis, the values of radioactivity in tumor and organs were examined. Anaerobic culture and histological observation of tumor and normal tissues were taken for examination of tumor-targeting characteristics of transgenic bifidobacterium infantis. Results The radioactivity in melanoma tissue increased progressively, while the radioactivity in normal organs became attenuated with time. The anaerobic culture showed an obvious proliferation of bifidobacterium infantis in tumor tissue. A lame part of area was Gram in the tumor tissue section, whereas the normal tissue was Gram negative. Conclusion Bifidobacterium infantis has good tumor-targeting to melanoma in mice, and recombined gene can be transported technically to solid tumors.
出处 《济宁医学院学报》 2010年第1期1-3,共3页 Journal of Jining Medical University
关键词 厌氧菌 肿瘤 靶向性 基因治疗 Anaerobic bacterium Tumor Targeting Gene therapy
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参考文献4

  • 1Kurozumi K, Tanaiya T, Ono Y, et al. Apoptosis induction with 5-fluorocytosine/cytosine deaminase gene therapy for human malignant glioma cells mediated by adenovirus[J]. J Neurooneol, 2007,66 ( 1-2 ): 117.
  • 2Bhujwalla ZM, Artemov D, Ballesteros P, et al. Combined vascular and extracellular pH imaging of solid tumors[J]. NMR Biomed,2008,20(2): 114.
  • 3GUO Zhi-ying, REN Qi-wei, WANG Hao-yi, et al. Tumortargeting Research of Bifidobacterium lnfantis on Melanoma in Mice[J]. Life Science Journal,2006,03(2):17.
  • 4吴瑜,易成,王树人,张敏,张静.婴儿双歧杆菌对小鼠黑色素瘤模型肿瘤组织的靶向性[J].四川大学学报(医学版),2003,34(3):435-438. 被引量:19

二级参考文献4

  • 1Gregorgy K. Progress in cancer gene therapy. Acta Oncol,1999; 38(6) :675.
  • 2Bhujwalla ZM, Artemov D, Ballesteros P, a al. Combined vascular and extracellular PH imaging of solid tumors. NMR Biomed, 2002; 15(2):114.
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  • 4Yazawa K, Fujimorl M, Nakamura T, et al. Bifidovacterium longum as a delivery system for cancer gene therapy: selective localization and growth in hypoxic tumors. Cancer Gene Therapy, 2000; 7(2):269.

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