gene expression profiling for in silico microdissection of hodgkins lymphoma microenvironment and identification of prognostic features基因表达分析的计算机显微解剖的霍奇金淋巴瘤预后的微环境和识别功能.pdfVIP
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gene expression profiling for in silico microdissection of hodgkins lymphoma microenvironment and identification of prognostic features基因表达分析的计算机显微解剖的霍奇金淋巴瘤预后的微环境和识别功能
Hindawi Publishing Corporation
Advances in Hematology
Volume 2011, Article ID 485310, 8 pages
doi:10.1155/2011/485310
Review Article
Gene Expression Profiling for In Silico Microdissection of
Hodgkin’s Lymphoma Microenvironment and Identification of
Prognostic Features
Franc¸ois Bertucci,1, 2, 3 Bruno Chetaille,1 and Luc Xerri1, 3
1 Department of Bio-Pathology, Institut Paoli-Calmettes, 232, bd Sainte-Marguerite, 13273 Marseille Cedex 09, France
2 Department of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France
3 Faculty of Medicine, University of Mediterranee, 13284 Marseille Cedex 07, France
Correspondence should be addressed to Luc Xerri, xerril@marseille.fnclcc.fr
Received 2 August 2010; Accepted 11 November 2010
Academic Editor: Shaji Kumar
Copyright © 2011 Franc¸ois Bertucci et al. This is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
Gene expression profiling studies based on DNA microarrays have demonstrated their ability to define the interaction pathways
between neoplastic and nonmalignant stromal cells in cancer tissues. During the past ten years, a number of approaches including
microdissection have tried to resolve the variability in DNA microarray measurements stemming from cancer tissue sample
heterogeneity. Another approach, designated as virtual or in silico microdissection, avoids the laborious and time-consuming step
of anatomic microdissection. It consists of confronting the gene expression profiles of complex tissue samples to those of cell lines
representative of different cell lineages, different differentiation stages, or different signaling pathways. This
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