Differentially expressed genes in association with in vitro invasiveness of human epithelioid sarcoma

Mol Pathol. 2001 Oct;54(5):324-30. doi: 10.1136/mp.54.5.324.

Abstract

Aims: Differential display reverse transcription polymerase chain reaction (RT-PCR) was performed to identify genes associated with the invasive potential of human epithelioid sarcoma.

Methods: Two different clonal subpopulations, GRU-1A and GRU-1B, derived from the same human epithelioid sarcoma cell line GRU-1 and known to differ greatly in their invasive potential were compared by means of mRNA fingerprinting.

Results: Using a set of 10 arbitrary upstream primers and nine anchored oligo-dT primers, 22 candidate gene fragments were identified; differential expression was confirmed in four of these fragments by northern blot analysis. At the mRNA level, apoferritin light chain was predominantly expressed by the highly invasive cell line GRU-1A. In contrast, the mitochondrial gene M1, encoding cytochrome c oxidase I, and the TI-227H gene were expressed more strongly by the low invasive cell line GRU-1B. Furthermore, a novel gene fragment was identified and cloned that was preferentially expressed in the low invasive cell line GRU-1B, and therefore might have an inhibitory role in invasion. Consequently, this gene fragment was designated as expressed in low invasive sarcoma cells (ELISC-1).

Conclusions: A novel gene fragment (ELISC-1) and three known genes were identified as potential regulators of tumour invasiveness. Cloning of the entire sequence of ELISC-1 and subsequent investigations are required to establish its biological role.

MeSH terms

  • Antigens, T-Independent / metabolism
  • Apoferritins / metabolism
  • Blotting, Northern
  • DNA Fingerprinting
  • Electron Transport Complex IV / metabolism
  • Gene Expression
  • Humans
  • Neoplasm Invasiveness / genetics*
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sarcoma / genetics*
  • Tumor Cells, Cultured

Substances

  • Antigens, T-Independent
  • RNA, Messenger
  • Apoferritins
  • Electron Transport Complex IV