In-situ-Hybridisierung in der klinischen Pathologie: Bedeutung der Polysomie 17 für die HER2-Bestimmung und genetische Tumorheterogenität im Mammakarzinom

The introduction of total genome sequencing led to the confirmation that tumors show substantial genetic heterogeneity. This phenomenon, which describes the presence of different genetic cell clones within a tumor also complicates the diagnostics of HER2. This article gives a review of new knowledge...

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Bibliographic Details
Main Authors: Gaiser, Timo (Author) , Rüschoff, Jan Hendrik (Author) , Moll, Roland (Author)
Format: Article (Journal)
Language:German
Published: 2012
In: Der Pathologe
Year: 2012, Volume: 33, Pages: 307-310
ISSN:1432-1963
DOI:10.1007/s00292-012-1663-z
Online Access:Verlag, Volltext: http://dx.doi.org/10.1007/s00292-012-1663-z
Verlag, Volltext: https://link.springer.com/article/10.1007/s00292-012-1663-z
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Author Notes:T. Gaiser, J. Rüschoff, R. Moll
Description
Summary:The introduction of total genome sequencing led to the confirmation that tumors show substantial genetic heterogeneity. This phenomenon, which describes the presence of different genetic cell clones within a tumor also complicates the diagnostics of HER2. This article gives a review of new knowledge on polysomy 17 and genetic tumor heterogeneity in connection with HER2 determination of breast cancer.
Item Description:First online: 11 October 2012
Gesehen am 11.06.2018
Physical Description:Online Resource
ISSN:1432-1963
DOI:10.1007/s00292-012-1663-z