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Identifikation neuer Zielstrukturen beim humanen hepatozellulären Karzinom mittels genomweiter molekularer Screeninganalysen

Overview of attention for article published in Die Pathologie, September 2012
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Title
Identifikation neuer Zielstrukturen beim humanen hepatozellulären Karzinom mittels genomweiter molekularer Screeninganalysen
Published in
Die Pathologie, September 2012
DOI 10.1007/s00292-012-1628-2
Pubmed ID
Authors

T. Longerich

Abstract

Molecular hepatocarcinogenesis represents a step-wise process which in most cases is associated with a well-defined chronic liver disease. By meta-analysis of classical comparative genomic hybridization (CGH) data an oncogenetic progression model could be generated (1q gain→ 8q gain → 4q loss → 16q loss → 13q loss). Array-based CGH allows the identification of etiology-dependent and independent genomic alterations. The Mouse Double Minute homologue 4 (MDM4) was shown to act as an oncogene of 1q32.1 gains in human hepatocellular carcinoma (HCC). Integration of genomic and epigenomic data facilitated the identification of tumor suppressor gene candidates in human HCC. For instance, Polo-like kinase 3 (PLK3) is frequently inactivated via promoter hypermethylation in combination with a loss of the second allele at 1p34.1. Both MDM4 overexpression and methylation-dependent inactivation of PLK3 represent potential targets for future therapeutic approaches.

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Geographical breakdown

Country Count As %
Germany 1 20%
Unknown 4 80%

Demographic breakdown

Readers by professional status Count As %
Student > Master 2 40%
Lecturer 1 20%
Researcher 1 20%
Unknown 1 20%
Readers by discipline Count As %
Medicine and Dentistry 3 60%
Agricultural and Biological Sciences 1 20%
Engineering 1 20%