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Cited 11 time in webofscience Cited 11 time in scopus
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Overexpression of Neuron-Specific Enolase as a Prognostic Factor in Patients with Gastric Cancer

Authors
Park, TaejinLee, Young-JoonJeong, Sang-HoChoi, Sang-KyungJung, Eun-JungJu, Young-taeJeong, Chi-YoungPark, MiyeongHah, Young-SoolYoo, JiyunHa, Woo-SongHong, Soon-ChanKo, Gyung Hyuck
Issue Date
Sep-2017
Publisher
대한위암학회
Keywords
Stomach neoplasms; Neuron-specific enolase; Neoplasm metastasis; Prognosis
Citation
Journal of Gastric Cancer, v.17, no.3, pp 228 - 236
Pages
9
Indexed
SCIE
SCOPUS
ESCI
KCI
Journal Title
Journal of Gastric Cancer
Volume
17
Number
3
Start Page
228
End Page
236
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/13522
DOI
10.5230/jgc.2017.17.e28
ISSN
2093-582X
2093-5641
Abstract
Purpose: Enolase is a cytoplasmic enzyme that catalyzes the conversion of 2-phosphoglycerate to phosphoenolpyruvate in the glycolytic pathway. The aim of this study was to investigate whether the overexpression of neuron-specific enolase (NSE) can serve as a prognostic factor in patients with gastric cancer (GC). Materials and Methods: To assess its prognostic value in GC, NSE expression was measured by immunohistochemistry in a clinically annotated tissue microarray comprising of 327 human GC specimens. Cytoplasmic NSE expression was scored from 0 to 4, reflecting the percentage of NSE-positive cells. Results: In terms of histology as per the World Health Organization criteria (P= 0.34), there were no differences between the NSE overexpression (NSE-OE) and NSE underexpression (NSE-UE) groups. The NSE-OE group showed a significantly lower rate of advanced GC (P< 0.01), lymph node metastasis (P= 0.01), advanced stage group (P< 0.01), cancer-related death (P< 0.01), and cancer recurrence (P< 0.01). Additionally, a Kaplan-Meier survival analysis revealed that the NSE-OE group had longer cumulative survival times than the NSE-UE group (log-rank test, P< 0.01). However, there were no significant differences in the serum levels of NSE expression in patients with GC and healthy volunteers (P= 0.28). Conclusions: Patients with NSE overexpressing GC tissues showed better prognostic results, implying that NSE could be a candidate biomarker of GC.
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