Literature DB >> 17510311

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

Donald R Schwartz1, Kamiar Moin, Bin Yao, Lynn M Matrisian, Lisa M Coussens, Thomas H Bugge, Barbara Fingleton, Heath B Acuff, Mark Sinnamon, Hind Nassar, Adrian E Platts, Stephen A Krawetz, Bruce E Linebaugh, Bonnie F Sloane.   

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.

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Year:  2007        PMID: 17510311     DOI: 10.1158/1541-7786.MCR-06-0337

Source DB:  PubMed          Journal:  Mol Cancer Res        ISSN: 1541-7786            Impact factor:   5.852


  7 in total

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Authors:  Kamiar Moin; Donald Schwartz; Stefanie R Mullins; Bonnie F Sloane
Journal:  Methods Mol Biol       Date:  2009

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Authors:  Anita Chalasani; Kyungmin Ji; Mansoureh Sameni; Samia H Mazumder; Yong Xu; Kamiar Moin; Bonnie F Sloane
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Authors:  Lisa Sevenich; Robert L Bowman; Steven D Mason; Daniela F Quail; Franck Rapaport; Benelita T Elie; Edi Brogi; Priscilla K Brastianos; William C Hahn; Leslie J Holsinger; Joan Massagué; Christina S Leslie; Johanna A Joyce
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7.  In Silico cancer cell versus stroma cellularity index computed from species-specific human and mouse transcriptome of xenograft models: towards accurate stroma targeting therapy assessment.

Authors:  Xinan Yang; Yong Huang; Younghee Lee; Vincent Gardeux; Ikbel Achour; Kelly Regan; Ellen Rebman; Haiquan Li; Yves A Lussier
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  7 in total

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