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首页> 外文期刊>Current Organic Synthesis >Studying nanoscale structural alterations in cancer cells to evaluate ovarian cancer drug treatment, using transmission electron microscopy imaging
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Studying nanoscale structural alterations in cancer cells to evaluate ovarian cancer drug treatment, using transmission electron microscopy imaging

机译:研究癌细胞中纳米级结构改变,评价卵巢癌药物治疗,使用透射电子显微镜成像

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摘要

Understanding nanoscale structural changes can provide information about the physical state of cells/tissues. It has now been shown that increases in nanoscale structural alterations are associated with the progress of carcinogenesis in most cancer cases, including early carcinogenesis. Anti-cancerous therapies are designed to inhibit the growth of cancer cells; however, it is challenging to detect the efficacy of such drugs in the early stages of treatment. A unique method of assessing the impact of anti-cancerous drugs on cancerous cells/tissues is to probe the nanoscale structural alterations. In this paper, we study the effect of different anti-cancerous drugs on ovarian tumorigenic cells, using their nanoscale structural alterations as a biomarker. Transmission electron microscopy (TEM) imaging on thin cell sections is performed to obtain their nanoscale structures. The degree of nanoscale structural alterations of tumorigenic cells and anti-cancerous drug treated tumorigenic cells are quantified by using the recently developed inverse participation ratio (IPR) technique. Results show an increase in the degree of nanoscale fluctuations in tumorigenic cells relative to non-tumorigenic cells; then a near-reversal of the degree of fluctuation in tumorigenic cells to that in non-tumorigenic cells, following anti-cancerous drug treatment. These results support that the effect of anti-cancerous drugs in cancer treatment can be quantified by using the degree of nanoscale fluctuations in the cells via TEM imaging. Potential applications of the technique for cancer treatment are also discussed.
机译:理解的纳米级结构的变化可以提供关于细胞/组织的物理状态的信息。现在已经证明,在纳米结构改变的增加与致癌作用在大多数癌症病例,包括早期癌变的进展有关。防癌治疗的目的是抑制癌细胞的生长;但是,它是具有挑战性的检测治疗的早期阶段,这种药物的功效。评估的抗癌症药物对癌细胞/组织的影响的唯一方法是探测纳米结构的改变。在本文中,我们研究了卵巢瘤细胞的不同的抗癌症药物的疗效,利用其纳米结构改变的生物标志物。透射电子显微镜(TEM)成像在薄单元部分被执行以获得它们的纳米级结构。致瘤性细胞和抗 - 癌药物处理致瘤性细胞的纳米级结构改变的程度是通过使用最近开发的逆参与比(IPR)技术进行定量。结果表明,在相对于非致瘤性细胞致瘤性细胞的纳米级的波动的程度的增加;然后波动的致瘤细胞,以在非致瘤性细胞,以下抗 - 癌药物治疗的程度的近逆转。这些结果支持了抗 - 癌药物在癌症治疗中的效果可以通过经由TEM成像使用在细胞中的纳米级的波动的程度进行定量。用于癌症治疗的技术的潜在应用进行了讨论。

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