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Article type: Research Article
Authors: Arafa, Mohammad | Boniver, Jacques | Delvenne, Philippe
Affiliations: Department of Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt | Department of Anatomic Pathology and Cytology, GIGA-Cancer, University of Liege, Liege, Belgium
Note: [] Corresponding author: Philippe Delvenne, MD, PhD, Department of Pathology B35, Chu Sart Tilman, 4000 Liege, Belgium. Tel.: +32 43662564; Fax: +32 43662919; E-mail: p.delvenne@ulg.ac.be
Abstract: Cervical and endometrial uterine carcinomas are heterogeneous groups of cancers, which are preceded by preneoplastic lesions. More accurate tools are needed to improve the diagnosis and to define markers which may be relevant for the diagnosis, prediction of disease progression and therapeutic response. High throughput technologies for testing and validating molecular targets in cancer lesions and in their precursors are presently available. Among them, the tissue microarray (TMA) presents the advantage of a morphological control of the analyzed tissue fragment. In this article, we review the different aspects of the TMA technology with a special consideration to a uterine carcinogenesis model.
DOI: 10.3233/DMA-2010-0709
Journal: Disease Markers, vol. 28, no. 5, pp. 267-272, 2010
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