Pregled bibliografske jedinice broj: 257351
Patterns of p73 N-terminal isoform expression and p53 status have prognostic value in gynecological cancer
Patterns of p73 N-terminal isoform expression and p53 status have prognostic value in gynecological cancer // International journal of oncology, 29 (2006), 4; 889-902 doi:10.3892/ijo.29.4.889 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 257351 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Patterns of p73 N-terminal isoform expression and p53 status have prognostic value in gynecological cancer
Autori
Becker, Kerstin ; Pancoska, Petr ; Concin, Nicole ; Vanden Heuvel, Kelly ; Slade, Neda ; Fischer, Margaret ; Chalas, Eva ; Moll, Ute, M.
Izvornik
International journal of oncology (1019-6439) 29
(2006), 4;
889-902
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
p73 ; p53 ; gynecological cancer
Sažetak
The goal of this study was to determine whether patterns of expression profiles of p73 isoforms and of p53 mutational status are useful combinatorial biomarkers for predicting outcome in a gynecological cancer cohort. This is the first such study using matched tumor/normal tissue pairs from each patient. The median follow-up was over two years. The expression of all 5 N-terminal isoforms (TAp73, ΔNp73, ΔN'p73, Ex2p73 and Ex2/3p73) was measured by real-time RT-PCR and p53 status was analyzed by immunohistochemistry. TAp73, ΔNp73 and ΔN'p73 were significantly upregulated in tumors. Surprisingly, their range of overexpression was age-dependent, with the highest differences δ (tumor-normal) in the youngest age group. Correction of this age effect was important in further survival correlations. We used all 6 variables (five p73 isoform levels plus p53 status) as input into a principal component analysis with Varimax rotation (VrPCA) to filter out noise from non-disease related individual variability of p73 levels. Rationally selected and individually weighted principal components from each patient were then used to train a support vector machine (SVM) algorithm to predict clinical outcome. This SVM algorithm was able to predict correct outcome in 30 of the 35 patients. We use here a mathematical tool for pattern recognition that has been commonly used in e.g. microarray data mining and apply it for the first time in a prognostic model. We find that PCA/SVM is able to test a clinical hypothesis with robust statistics and show that p73 expression profiles and p53 status are useful prognostic biomarkers that differentiate patients with good vs. poor prognosis with gynecological cancers.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE