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Distribution of Gemcitabine Is Nearly Homogenous in Two Orthotopic Murine Models of Pancreatic Cancer

机译:在两种胰腺癌原位小鼠模型中吉西他滨的分布几乎均一

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Pancreatic cancer is one of the leading causes of cancer-related death in the United States. Gemcitabine is a common treatment, but response rates are low, perhaps due in part to tumor hypoxia. We utilized C-14-labeled gemcitabine to map distribution of the drug with respect to perfused and hypoxic regions of the tumor microenvironment in two orthotopic xenograft models of pancreatic cancer. There was only a slight reduction in gemcitabine in hypoxic areas, with similar to 78% of the drug present in hypoxic compared to perfused areas. In addition, only a 4% reduction in gemcitabine was measured at >100 mu m from perfused blood vessels. Thus, despite significant areas of hypoxia in these tumors, gemcitabine distribution is relatively homogenous. Ours is the first study to directly measure gemcitabine distribution within tumor tissue, demonstrating that in these models, tumor tissue does not represent a barrier to gemcitabine penetration.
机译:胰腺癌是美国癌症相关死亡的主要原因之一。吉西他滨是一种常见的治疗方法,但缓解率很低,可能部分归因于肿瘤缺氧。我们利用C-14标记的吉西他滨在两个胰腺癌原位异种移植模型中针对肿瘤微环境的灌注区和缺氧区绘制药物分布图。低氧区域的吉西他滨仅略有减少,与灌注区域相比,低氧区域的药物占78%。此外,从灌注血管中测得,> 100μm的吉西他滨仅减少4%。因此,尽管这些肿瘤中存在明显的缺氧区域,但吉西他滨的分布相对均匀。我们的研究是第一个直接测量吉西他滨在肿瘤组织中分布的研究,表明在这些模型中,肿瘤组织并不代表吉西他滨渗透的障碍。

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