TRAF4 overexpression is a common characteristic of human carcinomas

被引:72
作者
Camilleri-Broet, S.
Cremer, I.
Marmey, B.
Comperat, E.
Viguie, F.
Audouin, J.
Rio, M-C
Fridman, W-H
Sautes-Fridman, C.
Regnier, C. H.
机构
[1] Univ Paris 06, Ctr Rech Biomed Cordeliers, INSERM,Univ Paris Descartes, U255,Fac Med,Ctr Rech Biomed Cordeliers, F-75006 Paris, France
[2] Univ Paris Descartes, Fac Med, AP HP Hotel Dieu, Paris, France
[3] Univ Paris 06, Fac Med, AP HA La Pitie Salpetriere, Paris, France
[4] Univ Strasbourg 1, INSERM, U596,Dept Pathol Mol,IGBMC, CNRS,UPR 6520, Illkirch Graffenstaden, France
关键词
TRAF4; chromosome; 17q11; ERBB2; amplification; lung;
D O I
10.1038/sj.onc.1209762
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor necrosis factor receptor (TNFR) associated factor 4 (TRAF4) was initially identified as a gene amplified and overexpressed in breast carcinomas. Our aim was to evaluate whether TRAF4 protein overexpression exists in other cancer types. Immunohistochemistry analysis of tumor samples from 623 patients with 20 different tumor types showed that TRAF4 was overexpressed in 268 tumors (43%), including 82 of 137 lung adenocarcinomas (60%). Interestingly, 32 primary tumors and their matching metastases exhibited mostly similar TRAF4 expression pattern. TRAF4 protein overexpression was limited to cancer cells and the subcellular localization was consistently cytoplasmic in a large majority of cases. To investigate changes in TRAF4 gene copy number, 125 cases from six different types of carcinomas were also analysed by fluorescence in situ hybridization. Out of the 28 cases (22%) showing an increased TRAF4 gene copy number, 23 (82%) were overexpressing the protein. Thus, TRAF4 gene amplification is one of the mechanisms responsible for TRAF4 protein overexpression in human cancers. Considering that TRAF4 is located at 17q11.2 in a region of amplification devoid of known oncogenes and is commonly overexpressed in cancer, our data support an oncogenic role for TRAF4.
引用
收藏
页码:142 / 147
页数:6
相关论文
共 29 条
[1]   MEKK4 is an effector of the embryonic TRAF4 for JNK activation [J].
Abell, AN ;
Johnson, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (43) :35793-35796
[2]   Signalling pathways of the TNF superfamily: A double-edged sword [J].
Aggarwal, BB .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :745-756
[3]   Chromosomal imbalances in human lung cancer [J].
Balsara, BR ;
Testa, JR .
ONCOGENE, 2002, 21 (45) :6877-6883
[4]  
Bieche I, 1996, CANCER RES, V56, P3886
[5]   Nek8, a NIMA family kinase member, is overexpressed in primary human breast tumors [J].
Bowers, AJ ;
Boylan, JF .
GENE, 2004, 328 :135-142
[6]  
Chung JY, 2002, J CELL SCI, V115, P679
[7]   Positional cloning of ZNF217 and NABC1:: Genes amplified at 20q13.2 and overexpressed in breast carcinoma [J].
Collins, C ;
Rommens, JM ;
Kowbel, D ;
Godfrey, T ;
Tanner, M ;
Hwang, S ;
Polikoff, D ;
Nonet, G ;
Cochran, J ;
Myambo, K ;
Jay, KE ;
Froula, J ;
Cloutier, T ;
Kuo, WL ;
Yaswen, P ;
Dairkee, S ;
Giovanola, J ;
Hutchinson, GB ;
Isola, J ;
Kallioniemi, OP ;
Palazzolo, M ;
Martin, C ;
Ericsson, C ;
Pinkel, D ;
Albertson, D ;
Li, WB ;
Gray, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (15) :8703-8708
[8]   TRAF4 functions as an intermediate of GITR-induced NF-κB activation [J].
Esparza, EM ;
Arch, RH .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (24) :3087-3092
[9]   Intracellular localization and transcriptional regulation of tumor necrosis factor (TNF) receptor-associated factor 4 (TRAF4) [J].
Glauner, H ;
Siegmund, D ;
Motejadded, H ;
Scheurich, P ;
Henkler, F ;
Janssen, O ;
Wajant, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (19) :4819-4829
[10]   Evaluation of HER-2/neu gene amplification and protein expression in non-small cell lung carcinomas [J].
Hirsch, FR ;
Varella-Garcia, M ;
Franklin, WA ;
Veve, R ;
Chen, L ;
Helfrich, B ;
Zeng, C ;
Baron, A ;
Bunn, PA .
BRITISH JOURNAL OF CANCER, 2002, 86 (09) :1449-1456