首页> 外文会议>ASME International Mechanical Engineering Congress and Exposition >CRYOINJURY ENHANCEMENT OF BREAST CANCER CELLS BY USE OF A MOLECULAR ADJUVANT (TNF-ALPHA)
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CRYOINJURY ENHANCEMENT OF BREAST CANCER CELLS BY USE OF A MOLECULAR ADJUVANT (TNF-ALPHA)

机译:通过使用分子佐剂(TNF-α)来冷冻血压增强乳腺癌细胞

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Cryoinjury of human breast cancer cells (MCF7) in engineered tissue equivalents and the enhancement of the cryoinjury by use of a molecular adjuvant (tumor necrosis factor alpha, TNF-alpha) was studied. Tissue equivalents (TEs) were constructed by seeding MCF7 cells in collagen solutions at the concentration of 100,000 cells/ml. After cultured in vitro for 2 days, the TEs were exposed with 100ng/ml TNF-alpha and cultured for 24 hours, and then underwent a single freeze-thaw cycle by a cryosurgery simulator. With the concentration and duration of TNF-alpha treatment studied, no apoptotic or necrotic cell death was observed by the administration of TNF-alpah only. After a freeze/thaw, MCF7 cells within the frozen region of the TEs were significantly injured immediately (i.e. <= 20 percent survival), but gradually repopulated and reached approximately 80 percent survival in Day3 without TNF-alpah pre-treatment. MCF7 with TNF-alpah pre-treatment showed the slight enhancement of immediate injury in the frozen region (i.e. <= 0 percent survival), and the repopulation was significantly inhibited so the viability remained below 40 percent even in Day 3. These results imply that TNF-alpha can be a potent adjuvant for cryosurgery.
机译:通过使用分子佐剂(肿瘤坏死因子α,TNF-α),研究人乳腺癌细胞(MCF7)的低温血癌细胞(MCF7)和冷冻血清的增强。通过在浓度为100,000个细胞/ ml的胶原溶液中播种MCF7细胞来构建组织当量(TES)。在体外培养2天后,将TES用100ng / ml TNF-α曝光并培养24小时,然后通过冷冻胶模拟器进行单一的冻融循环。随着TNF-α治疗的浓度和持续时间,仅通过施用TNF-ALPAH观察到凋亡或坏死性细胞死亡。在冷冻/解冻后,在TES的冷冻区域内的MCF7细胞立即显着损伤(即,存活率20%),但逐渐被重新灌注并在没有TNF-ALPAH预处理的情况下达到约80%的存活率。具有TNF-ALPAH预处理的MCF7表明,在冷冻区域(即<= 0%存活率)中立即损伤的略微增强,并且重新抑制,即使在第3天即使在第3天即使在第3天即使在3年内也仍然低于40%的活力。这些结果意味着TNF-alpha可以是冷冻胶的有效佐剂。

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