Method of detecting new cancer stem cell-like enrichment in development front assay (DFA).

Q4 Biochemistry, Genetics and Molecular Biology Journal of Stem Cells Pub Date : 2014-01-01 DOI:jsc.2015.9.4.235
Arka Saha, Swati Shree Padhi, Shomereeta Roy, Birendranath Banerjee
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Abstract

Unlabelled: Wound healing is an inherent property of injured tissue or a group of cells. The healing front is always developed by new cells which are progenitor of differentiated parental cells. In cancer tissues we aim to study the healing front and observed an enriched population of stem cell like properties in the developing front when compared to the other areas of the cell matrix.

Method: In vitro scratch assays with special focus on stem cell expression was used to analyze metastatic potential of the tumor cell, epithelial to mesenchymal transition and rate of cell migration to get an insight into the genes and the proteins getting expressed at the developing front. In this protocol we describe a fluorescence dependent method to document stem cell like enrichment at the developing front of a given wound in drug treated and untreated control cells under the same culture conditions in a time lag manner. We have tried to compare the rate of cell migration and the expression levels of stem cell markers between the treated and untreated cells.

Results: CD44 being a cell surface protein and being involved in cell migration and proliferation, higher intensity of CD44 was observed at the developing front with increasing time. The rate of cell migration differed with different treatments and so did the CD44 expression with expression being higher in 0.6mM concentration of bleomycin when compared to 0.4mM. Similar expression was observed for ALDH1 stem cell marker. This particular technique can not only be used for studying expression of CSC markers (like CD44, ALDH1) but also in assaying the expression profile of several proteins involved in cellular processes like EMT (Epithelial to Mesenchymal Transition), cell migration, tumorigeneisis and rate of proliferation.

Conclusion: Would healing is an integral property of solid tissues and in solid tumors properties of solid tissue wound are important characteristics of tumor development. Therefore combining the properties of stem cell like enrichment in the development front would be an important and fast assay to study migratory and metastatic properties of an invitro culture.

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发展前沿试验(DFA)检测新肿瘤干细胞样富集的方法。
未标记:伤口愈合是受伤组织或一组细胞的固有特性。愈合前沿通常是由分化的亲本细胞的祖细胞形成的新细胞。在癌症组织中,我们的目标是研究愈合前沿,并观察到与细胞基质的其他区域相比,在发育前沿具有丰富的干细胞样特性。方法:采用体外抓痕法分析肿瘤细胞的转移潜能、上皮细胞向间质细胞的转移和细胞迁移速率,以了解肿瘤细胞在发育前沿表达的基因和蛋白。在这个方案中,我们描述了一种荧光依赖的方法来记录在相同的培养条件下,在药物处理和未处理的对照细胞中,干细胞样的富集在给定伤口的发展前沿,以一种时间滞后的方式。我们试图比较处理和未处理的细胞之间的细胞迁移率和干细胞标志物的表达水平。结果:CD44是一种细胞表面蛋白,参与细胞迁移和增殖,随着时间的增加,CD44在发育前沿的表达强度增加。不同处理的细胞迁移速率不同,CD44的表达也不同,在0.6mM的博来霉素浓度下,CD44的表达高于0.4mM。ALDH1干细胞标记物也有类似表达。这种特殊的技术不仅可以用于研究CSC标志物(如CD44, ALDH1)的表达,还可以用于分析参与细胞过程的几种蛋白质的表达谱,如EMT(上皮到间充质转化),细胞迁移,肿瘤发生和增殖率。结论:愈合是实体组织的基本特性,在实体肿瘤中,实体组织伤口的特性是肿瘤发展的重要特征。因此,结合干细胞样富集的特性,将是研究体外培养的迁移和转移特性的一种重要而快速的方法。
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来源期刊
Journal of Stem Cells
Journal of Stem Cells Medicine-Transplantation
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0.10
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1
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