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MIM, a potential metastasis suppressor gene in bladder cancer

  • Hallym University
  • University of Michigan, Ann Arbor

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)291-294
Number of pages4
JournalNeoplasia
Volume4
Issue number4
DOIs
StatePublished - 2002

ASJC Scopus Subject Areas

  • Cancer Research

Keywords

  • Actin binding
  • Bladder cancer
  • Breast cancer
  • Invasion
  • Metastasis
  • Prostate cancer

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