Jacquot Catherine, Carbonnelle Delphine, Tomasoni Christophe, Papaconstadinou A, Roussis Vassilio, Roussakis Christos
Laboratoire de Pharmacologie Marine (EE0103) Faculté de Pharmacie, 44035 Nantes cedex, France.
Int J Oncol. 2004 Aug;25(2):519-27.
Non-small cell lung cancers remain particularly refractory to current treatments. Thus, characterisation of new molecular targets whose expression during chemotherapy could stop tumour growth, is required. In order to identify these new targets, we applied RT-PCR differential display (RT-PCR-DD) to a non-small cell lung cancer line (NSCLC-N6) treated by an original chemical substance, VT1, capable of arresting the proliferation of NSCLC-N6 cells in G1 phase. This study enabled us to identify a novel RNA, which has a strong homology with a DNA clone (GenBank accession no.: AY166681). This RNA resides in 6p24-p25 within intron 2 of the HEF1 gene, has no apparent open reading frame and may consists of a single large exon. Antisense oligonucleotides indicated that this RNA is involved in the proliferation arrest induced with VT1 treatment in NSCLC-N6 cells. The structure of this novel RNA resembles that of the previous identified extremely long non-coding RNAs which seem to regulate gene expression. Thus, this novel B2 transcript may belong to this new expanding non-coding RNA family.
非小细胞肺癌对当前的治疗方法仍然特别难治。因此,需要鉴定新的分子靶点,其在化疗期间的表达可以阻止肿瘤生长。为了鉴定这些新靶点,我们将逆转录聚合酶链反应差异显示(RT-PCR-DD)应用于一种非小细胞肺癌细胞系(NSCLC-N6),该细胞系用一种能够使NSCLC-N6细胞在G1期停止增殖的原始化学物质VT1处理。这项研究使我们能够鉴定出一种新型RNA,它与一个DNA克隆(GenBank登录号:AY166681)具有很强的同源性。这种RNA位于HEF1基因内含子2内的6p24-p25区域,没有明显的开放阅读框,可能由一个大的外显子组成。反义寡核苷酸表明,这种RNA参与了VT1处理诱导的NSCLC-N6细胞增殖停滞。这种新型RNA的结构类似于先前鉴定的似乎调节基因表达的极长非编码RNA。因此,这种新型B2转录本可能属于这个新的不断扩大的非编码RNA家族。