DocumentCode :
2472394
Title :
Laser capture microdissection (LCM) and the future of molecular pathology
Author :
Bonner, Robert F.
Author_Institution :
Lab. of Integrative & Med. Biophys., Nat. Inst. of Health, Bethesda, MD, USA
Volume :
2
fYear :
1998
fDate :
3-4 Dec 1998
Firstpage :
226
Abstract :
With the revolution in molecular biology and its application to the understanding of human disease, one stands at the threshold of a new era of molecular medicine which offers more specific and effective therapies based on sophisticated molecular diagnosis of an individual patient´s disease. Laser capture microdissection (LCM) has been developed to provide a rapid, reliable method to procure pure populations of targeted cells from specific microscopic regions of tissue sections for subsequent molecular analysis. Initially LCM is being used by the research community in order to understand the complex molecular changes in normal development and in the progression of disease pathologies. In the longer term, one is rapidly developing means of integrating LCM with molecular analysis techniques in order to provide a future technology for routine molecular diagnosis of clinical specimens
Keywords :
biological tissues; cancer; cellular biophysics; laser applications in medicine; molecular biophysics; reviews; clinical specimens; complex molecular changes; human disease; individual patient´s disease; laser capture microdissection; microscopic regions; molecular analysis techniques; molecular pathology; pure populations; routine molecular diagnosis; sophisticated molecular diagnosis; specific microscopic regions; targeted cells; tissue sections; Biopsy; Cancer; Diseases; Genetic mutations; Humans; Lesions; Medical diagnostic imaging; Optical films; Optical microscopy; Pathology;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Lasers and Electro-Optics Society Annual Meeting, 1998. LEOS '98. IEEE
Conference_Location :
Orlando, FL
Print_ISBN :
0-7803-4947-4
Type :
conf
DOI :
10.1109/LEOS.1998.739542
Filename :
739542
Link To Document :
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