Down-regulated melanoma differentiation associated gene (MDA-7) expression in human melanomas

被引:140
作者
Ekmekcioglu, S
Ellerhorst, J
Mhashilkar, AM
Sahin, AA
Read, CM
Prieto, VG
Chada, S
Grimm, EA
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[2] Introgen Therapeut, Houston, TX USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
关键词
melanoma development; tumor suppressor genes; mda-7; gene therapy; adenovirus;
D O I
10.1002/ijc.1437
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The melanoma differentiation associated gene-7 (mda-7) has a potential inhibitory role in melanoma progression, although the mechanisms underlying this effect are still unknown. mda-7 mRNA has been found to be present at higher levels in cultured normal melanocytes compared with metastatic melanoma cell lines. Furthermore, levels of mda-7 message have shown an inverse correlation with melanoma progression in human tumor samples, suggesting that mda-7 may be a novel tumor suppressor gene. We have designed this study to investigate MDA-7 protein expression in different stages of melanoma progression and to examine its antiproliferative effects in vitro. Our data demonstrate that MDA-7 protein can be found in normal melanocytes and early stage melanomas. It is also observed in smooth muscle cells in the skin. However, in keeping with a possible role as a tumor suppressor, MDA-7 expression is decreased in more advanced melanomas, with nearly undetectable levels in metastatic disease. We also investigated antitumor effects of overexpressed MDA-7 on human melanoma cells in vitro. Our results demonstrate that Ad-mda-7 induces apoptosis and G2/M cell cycle arrest in melanoma cells, but not in normal human melanocytes. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:54 / 59
页数:6
相关论文
共 12 条
[1]
Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[2]
Jiang HP, 1995, ONCOGENE, V11, P2477
[3]
The melanoma differentiation associated gene mda-7 suppresses cancer cell growth [J].
Jiang, HP ;
Su, ZZ ;
Lin, JJ ;
Goldstein, NI ;
Young, CSH ;
Fisher, PB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (17) :9160-9165
[4]
Madireddi MT, 2000, J CELL PHYSIOL, V185, P36, DOI 10.1002/1097-4652(200010)185:1<36::AID-JCP3>3.0.CO
[5]
2-V
[6]
Regulation of mda-7 gene expression during human melanoma differentiation [J].
Madireddi, MT ;
Dent, P ;
Fisher, PB .
ONCOGENE, 2000, 19 (10) :1362-1368
[7]
Madireddi MT, 2000, ADV EXP MED BIOL, V465, P239
[8]
Melanoma differentiation associated gene-7 (mda-7): A novel anti-tumor gene for cancer gene therapy [J].
Mhashilkar, AM ;
Schrock, RD ;
Hindi, M ;
Liao, J ;
Sieger, K ;
Kourouma, F ;
Zou-Yang, XH ;
Onishi, E ;
Takh, O ;
Vedvick, TS ;
Fanger, G ;
Stewart, L ;
Watson, GJ ;
Snary, D ;
Fisher, PB ;
Saeki, T ;
Roth, JA ;
Ramesh, R ;
Chada, S .
MOLECULAR MEDICINE, 2001, 7 (04) :271-282
[9]
Tumor-suppressive effects by adenovirus-mediated mda-7 gene transfer in non-small cell lung cancer cell in vitro [J].
Saeki, T ;
Mhashilkar, A ;
Chada, S ;
Branch, C ;
Roth, JA ;
Ramesh, R .
GENE THERAPY, 2000, 7 (23) :2051-2057
[10]
Bcl-2 family proteins as ion-channels [J].
Schendel, SL ;
Montal, M ;
Reed, JC .
CELL DEATH AND DIFFERENTIATION, 1998, 5 (05) :372-380