Evaluation of the prognostic significances of [gamma]-secretase genes in pancreatic cancer

With the growing requirement for novel prognostic biomarkers for pancreatic cancer, many studies have focused on clinical and/or genomic variables. Although many studies have been performed, carbohydrate antigen 19-9 is the only biomarker in clinical use. Therefore, the present study examined whethe...

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Veröffentlicht in:Oncology letters 2019-05, Vol.17 (5), p.4614
Hauptverfasser: Jeon, Yun Ho, Ha, Mihyang, Kim, Sung Won, Kim, Mun Ju, Lee, Chi-Seung, Oh, Chang-Kyu, Han, Myoung-Eun, Oh, Sae-Ock, Kim, Yun Hak
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Sprache:eng
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Zusammenfassung:With the growing requirement for novel prognostic biomarkers for pancreatic cancer, many studies have focused on clinical and/or genomic variables. Although many studies have been performed, carbohydrate antigen 19-9 is the only biomarker in clinical use. Therefore, the present study examined whether [gamma]-secretase genes, including presenilin (PSEN), nicastrin (NCSTN), presenilin enhancer protein 2 (PSENEN), and anterior pharynx-defective 1 (APH1-), could serve as prognostic factors for pancreatic cancer. The cohorts selected included >100 pancreatic cancer patients. Patient data were downloaded from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GSE21501). The prognostic roles of the [gamma]-secretase genes were analyzed by several survival analysis methods. Among the [gamma]-secretase genes, the prognosis tended to be worse in the 2 cohorts with increasing expression of PSEN1, APH1A, and PSENEN, while the remaining genes were the opposite in the 2 cohorts. Notably, although the patient characteristics were quite different, APH1A was statistically significantly associated with prognosis in the 2 cohorts. The hazard ratio of APH1A for overall survival was 1.598 (TCGA) and 2.724 (GSE21501). These results contribute to the study of [gamma]-secretase in pancreatic cancer. We believe that [gamma]-secretase, particularly APH1A, will be a new prognostic biomarker for pancreatic cancer.
ISSN:1792-1074
DOI:10.3892/ol.2019.10113