The expression levels of the translational factors eEF1A 1/2 correlate with cell growth but not apoptosis in hepatocellular carcinoma cell lines with different differentiation grade

被引:104
作者
Grassi, G. [2 ]
Scaggiante, B. [1 ]
Farra, R. [2 ]
Dapas, B. [2 ]
Agostini, F. [2 ]
Baiz, D. [1 ]
Rosso, N. [3 ]
Tiribelli, C. [1 ,3 ]
机构
[1] Univ Trieste, Mol Biol Sect, Dept Biochem Biophys & Macromol Chem, I-34127 Trieste, Italy
[2] Univ Trieste, Div Internal Med, Dept Clin Morphol & Technol Sci, I-34127 Trieste, Italy
[3] AREA Sci Pk, Ctr Fegato, I-34012 Trieste, Italy
关键词
hepatic cancer cells EEF1A2; EEF1A1; apoptosis; cell cycle;
D O I
10.1016/j.biochi.2007.07.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Despite the involvement of the elongation factors eEF1A (eEF1A1 and eEF1A2) in the development of different cancers no information is available on their possible contribution to the biology of hepatocellular carcinoma (HCC). We investigated the expression of both forms of eEF1A in HepG2 and JHH6 cell lines considered to be a good in vitro model of HCC at different stage of differentiation. Our data indicate that the mRNA amount of eEF1A1 is increased in both cell lines as compared to normal liver tissue, but eEF1A2 mRNA level is markedly increased only in JHH6. Moreover, the less differentiated cell line JHH6 displays higher EEF1A1 and EEF1A2 mRNAs levels and an higher nuclear-enriched/cytoplasm ratio of EEF1A protein compared to the better differentiated HepG2 cell line. Over-expression depends only partially on gene amplification. The more abundant mRNA levels and the higher nuclear-enriched/cytoplasm ratio of eEF1A in JHH6 neither correlate with apoptosis resistance nor with proliferation rate in sub-confluent cells. However, in confluent cells, a clear tendency to maintain JHH6 into the cell cycle was observed. In conclusion, we document the increased mRNA levels of EEF1A genes in HCC cell lines compared to normal liver. Additionally, we show the increased nuclear-enriched/cytoplasmic protein ratio of eEF1A and the marked raise of the expression of both eEF1A forms in JHH6 compared to HepG2, suggesting the possibility that eEF1A forms might become a relevant markers related to HCC tumor phenotype. (C) 2007 Published by Elsevier Masson SAS.
引用
收藏
页码:1544 / 1552
页数:9
相关论文
共 36 条
[1]
Translation factors: in sickness and in health [J].
Abbott, CM ;
Proud, CG .
TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (01) :25-31
[2]
eEF1A2 activates Akt and stimulates Akt-dependent actin remodeling, invasion and migration [J].
Amiri, A. ;
Noei, F. ;
Jeganathan, S. ;
Kulkarni, G. ;
Pinke, D. E. ;
Lee, J. M. .
ONCOGENE, 2007, 26 (21) :3027-3040
[3]
Gene encoding protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer [J].
Anand, N ;
Murthy, S ;
Amann, G ;
Wernick, M ;
Porter, LA ;
Cukier, IH ;
Collins, C ;
Gray, JW ;
Diebold, J ;
Demetrick, DJ ;
Lee, JM .
NATURE GENETICS, 2002, 31 (03) :301-305
[4]
INTERACTIONS OF EUKARYOTIC ELONGATION-FACTOR-2 WITH ACTIN - A POSSIBLE LINK BETWEEN PROTEIN SYNTHETIC MACHINERY AND CYTOSKELETON [J].
BEKTAS, M ;
NURTEN, R ;
GUREL, Z ;
SAYERS, Z ;
BERMEK, E .
FEBS LETTERS, 1994, 356 (01) :89-93
[5]
CHANGES IN ACTIVITY AND AMOUNT OF ACTIVE ELONGATION-FACTOR 1-ALPHA IN AGING AND IMMORTAL HUMAN FIBROBLAST-CULTURES [J].
CAVALLIUS, J ;
RATTAN, SIS ;
CLARK, BFC .
EXPERIMENTAL GERONTOLOGY, 1986, 21 (03) :149-157
[6]
ELONGATION-FACTOR 1-ALPHA, TRANSLATION AND THE CYTOSKELETON [J].
CONDEELIS, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (05) :169-170
[7]
Differentially expressed genes identified in human melanoma cell lines with different metastatic behaviour using high density oligonucleotide arrays [J].
de Wit, NJW ;
Burtscher, HJ ;
Weidle, UH ;
Ruiter, DJ ;
van Muijen, GNP .
MELANOMA RESEARCH, 2002, 12 (01) :57-69
[8]
A BIOMARKER THAT IDENTIFIES SENESCENT HUMAN-CELLS IN CULTURE AND IN AGING SKIN IN-VIVO [J].
DIMRI, GP ;
LEE, XH ;
BASILE, G ;
ACOSTA, M ;
SCOTT, C ;
ROSKELLEY, C ;
MEDRANO, EE ;
LINSKENS, M ;
RUBELJ, I ;
PEREIRASMITH, O ;
PEACOCKE, M ;
CAMPISI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9363-9367
[9]
Apoptosis rate can be accelerated or decelerated by overexpression or reduction of the level of elongation factor-1α [J].
Duttaroy, A ;
Bourbeau, D ;
Wang, XL ;
Wang, E .
EXPERIMENTAL CELL RESEARCH, 1998, 238 (01) :168-176
[10]
Edmonds BT, 1996, J CELL SCI, V109, P2705