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Erschienen in: Tumor Biology 4/2011

01.08.2011 | Research Article

Expression analysis and clinical evaluation of kallikrein-related peptidase 10 (KLK10) in colorectal cancer

verfasst von: Maroulio Talieri, Dimitra K. Alexopoulou, Andreas Scorilas, Dimitris Kypraios, Niki Arnogiannaki, Marina Devetzi, Matina Patsavela, Dimitris Xynopoulos

Erschienen in: Tumor Biology | Ausgabe 4/2011

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Abstract

Kallikrein-related peptidases (KLKs) represent a serine protease family having 15 members. KLK10 is a secreted protease with a trypsin-like activity. The function of KLK10 is poorly understood, although it has been suggested that KLK10 may function as a tumor suppressor gene. In human cancer, KLK10 gene shows organ-specific up- or down-regulation. Since KLKs are promising tumor biomarkers, the examination of KLK10 mRNA expression and its association with colorectal cancer (CRC) progression was studied using semi-quantitative PCR. One hundred and nineteen primary CRC specimens were examined for which follow-up information was available for a median period of 29 months (range, 1–104 months). KLK10 expression was found to be significantly associated with TNM stage (p = 0.028). Cox proportional hazard regression model using univariate analysis revealed for the first time that high status KLK10 expression is a significant factor for disease-free survival (DFS; p = 0.002) and overall survival (OS; p = 0.026) of patients. Kaplan–Meier survival curves demonstrated that KLK10 expression of low status is significantly associated with longer DFS (p = 0.001) as well as OS (p = 0.021), suggesting that KLK10 gene expression may be used as a marker of unfavorable prognosis for CRC. As the epigenetics of cancer are unraveled, KLK10 may represent not only a novel biomarker, but also a promising future therapeutic target for the disease.
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Metadaten
Titel
Expression analysis and clinical evaluation of kallikrein-related peptidase 10 (KLK10) in colorectal cancer
verfasst von
Maroulio Talieri
Dimitra K. Alexopoulou
Andreas Scorilas
Dimitris Kypraios
Niki Arnogiannaki
Marina Devetzi
Matina Patsavela
Dimitris Xynopoulos
Publikationsdatum
01.08.2011
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 4/2011
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-011-0175-4

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