TANGO is a tumor suppressor of malignant melanoma

被引:34
作者
Arndt, Stephanie [1 ]
Bosserhoff, Anja K. [1 ]
机构
[1] Univ Regensburg, Inst Pathol, D-93053 Regensburg, Germany
关键词
TANGO; tumor-suppressor gene; migration; malignant melanoma; cancer;
D O I
10.1002/ijc.22242
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The TANGO gene was originally identified as a new family member of the melanoma inhibitory activity gene family. The gene codes for a 14 kDa protein of so far unknown function. In our study we revealed that TANGO was downregulated or lost in 9 melanoma cell lines when compared to normal melanocytes and in most of the 8 tumor samples analyzed. The losses were associated with advanced stage of the disease. These results were confirmed in situ by immunohistochemistry on 10 paraffin-embedded sections of human malignant melanoma primary tumors and melanoma skin metastases. A small reduction of TANGO was also seen in different benign and atypical nevi when compared to normal skin. For functional analysis of TANGO we evaluated TANGO re-expressing melanoma cell clones and antisense TANGO cell clones with a complete loss of TANGO. Functional assays with TANGO transfected or treated cell lines revealed that TANGO expression reduces motility, whereas reduction of TANGO enhances migration. Our studies, therefore, indicate that reduction of TANGO expression contributes to tumor progression. These results taken together provide the first indications for a tumor suppressor role of TANGO gene in human malignant melanoma. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:2812 / 2820
页数:9
相关论文
共 16 条
[1]   Regulation of integrin activity by MIA [J].
Bauer, R ;
Humphries, M ;
Fässler, R ;
Winklmeier, A ;
Craig, SE ;
Bosserhoff, AK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (17) :11669-11677
[2]   Structure and promoter analysis of the gene encoding the human melanoma-inhibiting protein MIA [J].
Bosserhoff, AK ;
Hein, R ;
Bogdahn, U ;
Buettner, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (01) :490-495
[3]   Melanoma inhibitory activity (MIA): an important molecule in melanoma development and progression [J].
Bosserhoff, AK .
PIGMENT CELL RESEARCH, 2005, 18 (06) :411-416
[4]   Characterization and expression pattern of the novel MIA homolog TANGO [J].
Bosserhoff, AK ;
Moser, M ;
Buettner, R .
GENE EXPRESSION PATTERNS, 2004, 4 (04) :473-479
[5]  
Bosserhoff AK, 1997, CANCER RES, V57, P3149
[6]   Functional role of melanoma inhibitory activity in regulating invasion and metastasis of malignant melanoma cells in vivo [J].
Bosserhoff, AK ;
Echtenacher, B ;
Hein, R ;
Buettner, R .
MELANOMA RESEARCH, 2001, 11 (04) :417-421
[7]   REQUIREMENT FOR THE SYNERGY SITE FOR CELL-ADHESION TO FIBRONECTIN DEPENDS ON THE ACTIVATION STATE OF INTEGRIN ALPHA-5-BETA-1 [J].
DANEN, EHJ ;
AOTA, SI ;
VANKRAATS, AA ;
YAMADA, KM ;
RUITER, DJ ;
VANMUIJEN, GNP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (37) :21612-21618
[8]   Overexpression of melanoma inhibitory activity (MIA) enhances extravasation and metastasis of A-mel 3 melanoma cells in vivo [J].
Guba, M ;
Bosserhoff, AK ;
Steinbauer, M ;
Abels, C ;
Anthuber, M ;
Buettner, R ;
Jauch, KW .
BRITISH JOURNAL OF CANCER, 2000, 83 (09) :1216-1222
[9]  
GUTMAN M, 1995, CANCER RES, V55, P2470
[10]   Role of intermediate filaments in migration, invasion and metastasis [J].
Hendrix, MJC ;
Seftor, EA ;
Chu, YW ;
Trevor, KT ;
Seftor, REB .
CANCER AND METASTASIS REVIEWS, 1996, 15 (04) :507-525