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Hu/Mu ProtIn寡核苷酸微阵列:用于分析肿瘤及其微环境中蛋白酶和蛋白酶抑制剂基因表达的双物种阵列。

Hu/Mu ProtIn oligonucleotide microarray: dual-species array for profiling protease and protease inhibitor gene expression in tumors and their microenvironment.

作者信息

Schwartz Donald R, Moin Kamiar, Yao Bin, Matrisian Lynn M, Coussens Lisa M, Bugge Thomas H, Fingleton Barbara, Acuff Heath B, Sinnamon Mark, Nassar Hind, Platts Adrian E, Krawetz Stephen A, Linebaugh Bruce E, Sloane Bonnie F

机构信息

Barbara Ann Karmanos Cancer Institute, Wayne State University, Detroit, Michigan, USA.

出版信息

Mol Cancer Res. 2007 May;5(5):443-54. doi: 10.1158/1541-7786.MCR-06-0337.

DOI:10.1158/1541-7786.MCR-06-0337
PMID:17510311
Abstract

Proteolysis is a critical regulatory mechanism for a wide variety of physiologic and pathologic processes. To assist in the identification of proteases, their endogenous inhibitors, and proteins that interact with proteases or proteolytic pathways in biological tissues, a dual-species oligonucleotide microarray has been developed in conjunction with Affymetrix. The Hu/Mu ProtIn microarray contains 516 and 456 probe sets that survey human and mouse genes of interest (proteases, protease inhibitors, or interactors), respectively. To investigate the performance of the array, gene expression profiles were analyzed in pure mouse and human samples (reference RNA; normal and tumor cell lines/tissues) and orthotopically implanted xenografts of human A549 lung and MDA-MB-231 breast carcinomas. Relative gene expression and "present-call" P values were determined for each probe set using dChip and MAS5 software, respectively. Despite the high level of sequence identity of mouse and human protease/inhibitor orthologues and the theoretical potential for cross-hybridization of some of the probes, >95% of the "present calls" (P<0.01) resulted from same-species hybridizations (e.g., human transcripts to human probe sets). To further assess the performance of the microarray, differential gene expression and false discovery rate analyses were carried out on human or mouse sample groups, and data processing methods to optimize performance of the mouse and human probe sets were identified. The Hu/Mu ProtIn microarray is a valuable discovery tool for the identification of components of human and murine proteolytic pathways in health and disease and has particular utility in the determination of cellular origins of proteases and protease inhibitors in xenograft models of human cancer.

摘要

蛋白质水解是多种生理和病理过程的关键调节机制。为了有助于鉴定蛋白酶、其内源抑制剂以及与生物组织中的蛋白酶或蛋白水解途径相互作用的蛋白质,已与Affymetrix联合开发了一种双物种寡核苷酸微阵列。Hu/Mu ProtIn微阵列分别包含516个和456个探针组,用于检测人源和鼠源的感兴趣基因(蛋白酶、蛋白酶抑制剂或相互作用分子)。为了研究该阵列的性能,在纯小鼠和人样本(参考RNA;正常和肿瘤细胞系/组织)以及人A549肺癌和MDA-MB-231乳腺癌的原位植入异种移植物中分析了基因表达谱。分别使用dChip和MAS5软件确定每个探针组的相对基因表达和“存在呼叫”P值。尽管小鼠和人蛋白酶/抑制剂直系同源物的序列同一性水平很高,并且一些探针存在理论上的交叉杂交可能性,但>95%的“存在呼叫”(P<0.01)来自同物种杂交(例如,人类转录本与人探针组杂交)。为了进一步评估微阵列的性能,对人或小鼠样本组进行了差异基因表达和错误发现率分析,并确定了优化小鼠和人探针组性能的数据处理方法。Hu/Mu ProtIn微阵列是一种有价值的发现工具,可用于鉴定健康和疾病状态下人源和鼠源蛋白水解途径的组成部分,在确定人类癌症异种移植模型中蛋白酶和蛋白酶抑制剂的细胞来源方面具有特殊用途。

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