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

被引:5
作者
Weber, A [1 ]
Engers, R [1 ]
Nockemann, S [1 ]
Gohr, LL [1 ]
Zur Hausen, A [1 ]
Gabbert, HE [1 ]
机构
[1] Univ Dusseldorf, Inst Pathol, D-40225 Dusseldorf, Germany
来源
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY | 2001年 / 54卷 / 05期
关键词
invasion; epithelioid sarcoma; differential gene expression; heterogeneity;
D O I
10.1136/mp.54.5.324
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
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 Ml, 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.
引用
收藏
页码:324 / 330
页数:7
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