Decreased expression of p39 is associated with a poor prognosis in human hepatocellular carcinoma

被引:14
作者
Lu, Jeng-Wei [1 ]
Chang, Jan-Gowth [2 ,3 ]
Yeh, Kun-Tu [4 ]
Chen, Rong-Ming [6 ]
Tsai, Jeffrey J. P. [1 ]
Hu, Rouh-Mei [1 ,5 ]
机构
[1] Asia Univ, Dept Biotechnol, Taichung 413, Taiwan
[2] Kaohsiung Med Univ, Dept Med Res, Kaohsiung 807, Taiwan
[3] Kaohsiung Med Univ, Dept Lab Med, Kaohsiung 807, Taiwan
[4] Changhua Christian Hosp, Dept Pathol, Changhua 500, Taiwan
[5] China Med Univ, Sch Chinese Med, Taichung 404, Taiwan
[6] Natl Univ Tainan, Dept Comp Sci & Informat Engn, Tainan 700, Taiwan
关键词
Human hepatocellular carcinoma; Immunohistochemistry; Prognosis; p39; CDK5R2; CYCLIN-DEPENDENT KINASE-5; CDK5; CELLS; LIVER; EPIDEMIOLOGY; ACTIVATOR; CANCER; LOCALIZATION; HEPATITIS; APOPTOSIS;
D O I
10.1007/s12032-010-9707-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aims of this study are to investigate the relationship between p39 expression and clinicopathological parameters of hepatocellular carcinoma (HCC) and to evaluate the prognostic value of p39 for HCC patients. Real-time quantitative PCR and immunohistochemistry was used to measure p39 expression in tumor and adjacent nontumor samples. Relationships of p39 expression with clinical parameters and patient survival were analyzed. Real-time quantitative RT-PCR showed that the quantity of p39 mRNA in cancerous tissue was significantly lower than that in nontumor tissue (P < 0.001). Immunohistochemistry data confirmed that p39 protein was reduced in 64% of HCC. p39 expression was not influenced by chronic alcohol exposure or cirrhosis. Reduction in p39 was correlated with the HBV (P = 0.039), HCV (P = 0.011), and histological grade (P < 0.001). HCC patients with lower p39 expression had poorer overall survival rate than that with high expression (HR, 2.868; 95% CI, 1.451-5.670; P = 0.002). Together with other results, these results reveal that p39 expression was reduced in HCC tissue. p39 could be a useful clinical prognostic marker for hepatocellular carcinoma patients.
引用
收藏
页码:S239 / S245
页数:7
相关论文
共 51 条
[1]   Cdk5 phosphorylates non-genotoxically overexpressed p53 following inhibition of PP2A to induce cell cycle arrest/apoptosis and inhibits tumor progression [J].
Ajay, Amrendra K. ;
Upadhyay, Ankur K. ;
Singh, Sandeep ;
Vijayakumar, Maleppillil V. ;
Kumari, Ratna ;
Pandey, Vimal ;
Boppana, Ramanamurthy ;
Bhat, Manoj K. .
MOLECULAR CANCER, 2010, 9
[2]   Cellular senescence requires CDK5 repression of Rac1 activity [J].
Alexander, K ;
Yang, HS ;
Hinds, PW .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (07) :2808-2819
[3]   Epidemiology of primary liver cancer [J].
Bosch, FX ;
Ribes, J ;
Borràs, J .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :271-285
[4]   Expression of the neuronal cyclin-dependent kinase 5 activator p35Nck5a in human monocytic cells is associated with differentiation [J].
Chen, F ;
Studzinski, GP .
BLOOD, 2001, 97 (12) :3763-3767
[5]   Gene expression patterns in human liver cancers [J].
Chen, X ;
Cheung, ST ;
So, S ;
Fan, ST ;
Barry, C ;
Higgins, J ;
Lai, KM ;
Ji, JF ;
Dudoit, S ;
Ng, IOL ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
MOLECULAR BIOLOGY OF THE CELL, 2002, 13 (06) :1929-1939
[6]   An unusual member of the Cdk family: Cdk5 [J].
Dhariwala, Fatema A. ;
Rajadhyaksha, Medha S. .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2008, 28 (03) :351-369
[7]   Hepatocellular carcinoma: Epidemiology and molecular carcinogenesis [J].
El-Serag, Hashem B. ;
Rudolph, Lenhard .
GASTROENTEROLOGY, 2007, 132 (07) :2557-2576
[8]   Trends in survival of patients with hepatocellular carcinoma between 1977 and 1996 in the United States [J].
El-Serag, HB ;
Mason, AC ;
Key, C .
HEPATOLOGY, 2001, 33 (01) :62-65
[9]   Inhibiting the Cyclin-Dependent Kinase CDK5 Blocks Pancreatic Cancer Formation and Progression through the Suppression of Ras-Ral Signaling [J].
Feldmann, Georg ;
Mishra, Anjali ;
Hong, Seung-Mo ;
Bisht, Savita ;
Strock, Christopher J. ;
Ball, Douglas W. ;
Goggins, Michael ;
Maitra, Anirban ;
Nelkin, Barry D. .
CANCER RESEARCH, 2010, 70 (11) :4460-4469
[10]   Cdk5 regulates activation and localization of Src during corneal epithelial wound closure [J].
Gao, CY ;
Stepp, MA ;
Fariss, R ;
Zelenka, P .
JOURNAL OF CELL SCIENCE, 2004, 117 (18) :4089-4098