MIM, a potential metastasis suppressor gene in bladder cancer

被引:156
作者
Lee, YG
Macoska, JA
Korenchuk, S
Pienta, KJ
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI USA
[3] Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USA
[4] Hallym Univ, Coll Med, Dept Urol, Seoul, South Korea
来源
NEOPLASIA | 2002年 / 4卷 / 04期
关键词
metastasis; actin binding; bladder cancer; invasion; prostate cancer; breast cancer;
D O I
10.1038/sj.neo.7900231
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using a modified version of the mRNA differential display technique, five human bladder cancer cell lines from low grade to metastatic were analyzed to identify differences in gene expression. A 316-bp cDNA (C11 - 300) was isolated that was not expressed in the metastatic cell line TccSuP Sequence analysis revealed that this gene was identical to KIAA 0429, has a 5.3-kb transcript that mapped to 8q24.1. The protein is predicted to be 356 amino acids in size and has an actin-binding WH2 domain. Northern blot revealed expression in multiple normal tissues, but none in a metastatic breast cancer cell line (SKBR3) or in metastatic prostatic cancer cell lines (LNCaP, PC3). We have named this gene Missing in Metastasis (MIM) and our data suggest that it may be involved in cytoskeletal organization.
引用
收藏
页码:291 / 294
页数:4
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