[HTML][HTML] Overexpression of lysine specific demethylase 1 predicts worse prognosis in primary hepatocellular carcinoma patients
ZK Zhao, HF Yu, DR Wang, P Dong… - World journal of …, 2012 - ncbi.nlm.nih.gov
ZK Zhao, HF Yu, DR Wang, P Dong, L Chen, WG Wu, WJ Ding, YB Liu
World journal of gastroenterology: WJG, 2012•ncbi.nlm.nih.govAIM: To investigate the clinicopathological features and prognostic value of lysine specific
demethylase 1 (LSD1) in hepatocellular carcinoma (HCC). METHODS: We examined LSD1
expression in 60 paired liver cancer tissues and adjacent noncancerous tissues by
quantitative real time polymerase chain reaction (qRT-PCR) and Western blotting. In
addition, we analyzed LSD1 expression in 198 HCC samples by immunohistochemistry. The
relationship between LSD1 expression, clinicopathological features and patient survival was …
demethylase 1 (LSD1) in hepatocellular carcinoma (HCC). METHODS: We examined LSD1
expression in 60 paired liver cancer tissues and adjacent noncancerous tissues by
quantitative real time polymerase chain reaction (qRT-PCR) and Western blotting. In
addition, we analyzed LSD1 expression in 198 HCC samples by immunohistochemistry. The
relationship between LSD1 expression, clinicopathological features and patient survival was …
Abstract
AIM: To investigate the clinicopathological features and prognostic value of lysine specific demethylase 1 (LSD1) in hepatocellular carcinoma (HCC).
METHODS: We examined LSD1 expression in 60 paired liver cancer tissues and adjacent noncancerous tissues by quantitative real time polymerase chain reaction (qRT-PCR) and Western blotting. In addition, we analyzed LSD1 expression in 198 HCC samples by immunohistochemistry. The relationship between LSD1 expression, clinicopathological features and patient survival was investigated.
RESULTS: Immunohistochemistry, Western blotting, and qRT-PCR consistently confirmed LSD1 overexpression in HCC tissues compared to adjacent non-neoplastic tissues (P< 0.01). Additionally, immunostaining showed more LSD1-positive cells in the higher tumor stage (T3-4) and tumor grade (G3) than in the lower tumor stage (T1-2, P< 0.001) and tumor grade (G1-2, P< 0.001), respectively. Moreover, HCC patients with high LSD1 expression had significantly lower 5-year overall survival rates (P< 0.001) and lower 5-year disease-free survival rates (P< 0.001), respectively. A Cox proportional hazards model further demonstrated that LSD1 over-expression was an independent predictor of poor prognosis for both 5-year disease-free survival [hazards ratio (HR)= 1.426, 95% CI: 0.672-2.146, P< 0.001] and 5-year overall survival (HR= 2.456, 95% CI: 1.234-3.932, P< 0.001) in HCC.
CONCLUSION: Our data suggest for the first time that the overexpression of LSD1 protein in HCC tissues indicates tumor progression and predicts poor prognosis.
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