Literature DB >> 20578260

Overexpression of aspartyl-(asparaginyl)-beta-hydroxylase in hepatocellular carcinoma is associated with worse surgical outcome.

Kui Wang1, Jian Liu, Zhen-Lin Yan, Jun Li, Le-Hua Shi, Wen-Ming Cong, Yong Xia, Qi-Fei Zou, Tao Xi, Feng Shen, Hong-Yang Wang, Meng-Chao Wu.   

Abstract

UNLABELLED: The association between the overexpression of aspartyl-(asparaginyl)-beta-hydroxylase (AAH) and the invasiveness of hepatocellular carcinoma (HCC) in vitro has been reported. However, the prognostic value of AAH expression in HCC remains unclear. The purpose of this study was to investigate the relationship between AAH expression, tumor recurrence, and patient survival. We identified AAH as the most overexpressed gene in HCC by way of complementary DNA microarray hybridization. A prospective study of 233 patients undergoing curative resection indicated that AAH expression was an independent factor affecting recurrence (hazard ratio [HR] 3.161, 95% confidence interval [CI] 2.115-4.724, P < 0.001) and survival (HR 2.712, 95% CI 1.734-4.241, P < 0.001). Patients with AAH overexpression had a poorer prognosis than those with AAH underexpression (P < 0.001 for both recurrence and survival). In Barcelona Clinic Liver Cancer stage A patients with AAH overexpression or underexpression, the tumor recurrence and survival rates were also statistically different (45% and 85% versus16% and 33% in 1- and 3-year cumulative recurrence rates, respectively; 73% and 37% versus 90% and 80% in 1- and 3-year survival rates, respectively; P < 0.001 for both). Furthermore, in stage A patients with tumors measuring < or =5 cm in diameter, the time to recurrence was 26.7 +/- 1.6 versus 51.9 +/- 2.8 months, and the 1- and 3- year survival rates were 97% and 52% versus 100% and 90% in AAH overexpression and underexpression patients, respectively (P < 0.001 for both).
CONCLUSION: AAH overexpression in HCC is strongly correlated with worse surgical outcome, and this molecule likely provides a more precise prognostic predictor in early stage HCCs.

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Year:  2010        PMID: 20578260     DOI: 10.1002/hep.23650

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  55 in total

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6.  Activation of signal transduction pathways during hepatic oncogenesis.

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Journal:  Cancer Lett       Date:  2015-10-01       Impact factor: 8.679

7.  Aspartate β-hydroxylase modulates cellular senescence through glycogen synthase kinase 3β in hepatocellular carcinoma.

Authors:  Yoshifumi Iwagami; Chiung-Kuei Huang; Mark J Olsen; John-Michael Thomas; Grace Jang; Miran Kim; Qiushi Lin; Rolf I Carlson; Carl E Wagner; Xiaoqun Dong; Jack R Wands
Journal:  Hepatology       Date:  2016-02-19       Impact factor: 17.425

8.  Risk factors and management for early and late intrahepatic recurrence of solitary hepatocellular carcinoma after curative resection.

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Authors:  Zheng Li; Zhengqing Lei; Yong Xia; Jun Li; Kui Wang; Han Zhang; Xuying Wan; Tian Yang; Weiping Zhou; Mengchao Wu; Timothy M Pawlik; Wan Yee Lau; Feng Shen
Journal:  JAMA Surg       Date:  2018-10-17       Impact factor: 14.766

10.  Downregulation of nuclear receptor FXR is associated with multiple malignant clinicopathological characteristics in human hepatocellular carcinoma.

Authors:  Hongying Su; Chuang Ma; Jingfeng Liu; Ningbo Li; Meiqin Gao; Aimin Huang; Xichun Wang; Wendong Huang; Xiongfei Huang
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2012-10-04       Impact factor: 4.052

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