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Clinicopathological and prognostic significance of heme oxygenase-1 expression in small intestinal adenocarcinomas

Authors
Jun, Sun-YoungHong, Seung-MoBae, Young KyungKim, Hee KyungJang, Kyu YunEom, Dae Woon
Issue Date
May-2018
Publisher
Blackwell Publishing Inc.
Keywords
heme oxygenase-1; immunohistochemistry; small intestine; survival
Citation
Pathology International, v.68, no.5, pp 294 - 300
Pages
7
Journal Title
Pathology International
Volume
68
Number
5
Start Page
294
End Page
300
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/6025
DOI
10.1111/pin.12657
ISSN
1320-5463
1440-1827
Abstract
Heme oxygenase-1 (HO-1), a stress-response protein, is highly induced in various carcinomas. It is implicated in carcinogenesis and tumor progression. High HO-1 expression is associated with better prognosis of patients with colorectal and gastric cancers. Induction or inhibition of HO-1 can mediate chemo-sensitivity, therefore it might be a therapeutic target to develop anticancer agents. To define the clinicopathological and prognostic significance of HO-1 expression in small-intestinal adenocarcinomas (SIACs), immunohistochemical microarray analysis of HO-1 expression was performed for 191 surgically resected SIAC cases and results were compared with various clinicopathologic variables, including survival. HO-1 was highly expressed in 127 (66.5%) cases. Patients with high HO-1 expression were associated with younger age (P=0.048), lower pT category (P=0.017), and less pancreatic invasion (P=0.047). Patients with high HO-1 expression tended to have longer overall survival (median, 38.5 months) than those with low HO-1 expression (24.5 months), although the difference in overall survival was not statistically significant (P=0.677). In summary, high HO-1 expression is frequently observed in SIACs. It is related to favorable clinicopathologic parameters, including younger age, lower T category, and less pancreatic invasion. Therefore, HO-1 may serve as a prognostic marker and a new target to modulate chemotherapeutic effects in patients with SIACs.
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