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Micro-Raman Detection of Nuclear Membrane Lipid Fluctuations in Senescent Epithelial Breast Cancer Cells

机译:衰老上皮癌细胞中核膜脂质波动的微拉曼检测。

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Originally identified in cultured cells, oncogenic cellular senescence is a growth-arrest mechanism which may inhibit tumor development by limiting the ability of cells to divide. However, literature shows that these cells secrete tumor-inducing and tumor-suppressing proteins leading to poor prognosis. Understanding the progression of oncogenic cellular senescence and associated mechanisms provides important implications for improving tumorigenesis therapeutic treatments. Micro-Raman spectroscopic imaging has grown in popularity as an imaging technique compared to the standard imaging predecessors and can be attributed to its numerous benefits such as no sample perturbation and the provision of direct chemical information. Through the use of label-free micro-Raman spectroscopy, control and senescent cells were noninvasively imaged. Resulting spectral images were processed using chemometric techniques, and average nuclei spectra from each sample set were compared. In turn, changes in the -cis and -trans unsaturated lipid isomer content were found to differ among proliferating and senescent cells. This may lead to increased nuclear fluidity and may contribute to the inability of senescent cells to complete the cell cycle. In the tumor environment, this detected increase in nuclear envelope fluidity could lead to downstream gene expression modifications and increased nucleo-cytoplasmic RNA translocation. Understanding nuclear envelope fluidity could provide insight into secretory profiles of senescent cells and their role in carcinogenesis, meriting further investigation into novel therapeutic technique development for oncogenic cellular senescence.
机译:最初在培养细胞中鉴定,致癌细胞衰老是一种生长停滞机制,可通过限制细胞分裂的能力来抑制肿瘤的发展。然而,文献显示这些细胞分泌诱导肿瘤和抑制肿瘤的蛋白,导致预后不良。了解致癌细胞衰老的进程和相关机制为改善肿瘤发生治疗提供了重要的启示。与标准成像先驱相比,微拉曼光谱成像作为一种成像技术已越来越普及,并且可以归因于其众多优势,例如无需样品干扰和提供直接的化学信息。通过使用无标记的显微拉曼光谱法,无创成像了对照细胞和衰老细胞。使用化学计量学技术处理得到的光谱图像,并比较每个样品组的平均核光谱。继而,发现增殖细胞和衰老细胞中-顺式和-反式不饱和脂质异构体含量的变化是不同的。这可能导致核流动性增加,并且可能导致衰老细胞无法完成细胞周期。在肿瘤环境中,这种检测到的核包膜流动性增加可能导致下游基因表达修饰和核质RNA易位增加。了解核包膜的流动性可以提供对衰老细胞的分泌概况及其在致癌作用中的作用的洞察力,值得对致癌细胞衰老的新型治疗技术发展进行进一步研究。

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