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Laser capture microdissection, microarrays and the precise definition of a cancer cell.

机译:激光捕获显微切割,微阵列和癌细胞的精确定义。

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摘要

Most expression profiling studies of solid tumors have used biopsy samples containing large numbers of contaminating stromal and other cell types, thereby complicating any precise delineation of gene expression in nontumor versus tumor cell types. Combining laser capture microdissection, RNA amplification protocols, microarray technologies and our knowledge of the human genome sequence, it is possible to isolate pure populations of cells or even a single cell and interrogate the expression of thousands of sequences for the purpose of more precisely defining the biology of the tumor cell. Although many of the studies that currently allow for characterization of small sample preparations and single cells were performed utilizing noncancer cell types, and in some cases isolation protocols other than laser capture microdissection, a list of protocols are described that could be used for the expression analysis of individual tumor cells. Application of these experimental approaches to cancer studies may permit a more accurate definition of the biology of the cancer cell, so that ultimately, more specific targeted therapies can be developed.
机译:对实体瘤的大多数表达谱研究都使用了含有大量污染性基质细胞和其他细胞类型的活检样品,从而使非肿瘤细胞与肿瘤细胞类型中基因表达的任何精确描述变得复杂。结合激光捕获显微切割术,RNA扩增方案,微阵列技术和我们对人类基因组序列的了解,可以分离纯细胞甚至单个细胞并询问成千上万个序列的表达,以便更精确地定义肿瘤细胞生物学。尽管许多目前允许表征小样本制备物和单细胞的研究都是使用非癌细胞类型进行的,在某些情况下,除了激光捕获显微切割法以外,还分离出一些方案,但仍描述了一系列可用于表达分析的方案单个肿瘤细胞。这些实验方法在癌症研究中的应用可能允许对癌细胞的生物学进行更准确的定义,从而最终可以开发出更具体的靶向疗法。

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