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对3p12.3肿瘤抑制区域一个新的纯合缺失的分析揭示了两个新的内含子非编码RNA基因。

Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes.

作者信息

Angeloni Debora, ter Elst Arja, Wei Ming Hui, van der Veen Anneke Y, Braga Eleonora A, Klimov Eugene A, Timmer Tineke, Korobeinikova Luba, Lerman Michael I, Buys Charles H C M

机构信息

Laboratory of Immunobiology, Center for Cancer Research, National Cancer Institute at Frederick, Frederick, MD, USA.

出版信息

Genes Chromosomes Cancer. 2006 Jul;45(7):676-91. doi: 10.1002/gcc.20332.

Abstract

Homozygous deletions or loss of heterozygosity (LOH) at human chromosome band 3p12 are consistent features of lung and other malignancies, suggesting the presence of a tumor suppressor gene(s) (TSG) at this location. Only one gene has been cloned thus far from the overlapping region deleted in lung and breast cancer cell lines U2020, NCI H2198, and HCC38. It is DUTT1 (Deleted in U Twenty Twenty), also known as ROBO1, FLJ21882, and SAX3, according to HUGO. DUTT1, the human ortholog of the fly gene ROBO, has homology with NCAM proteins. Extensive analyses of DUTT1 in lung cancer have not revealed any mutations, suggesting that another gene(s) at this location could be of importance in lung cancer initiation and progression. Here, we report the discovery of a new, small, homozygous deletion in the small cell lung cancer (SCLC) cell line GLC20, nested in the overlapping, critical region. The deletion was delineated using several polymorphic markers and three overlapping P1 phage clones. Fiber-FISH experiments revealed the deletion was approximately 130 kb. Comparative genomic sequence analysis uncovered short sequence elements highly conserved among mammalian genomes and the chicken genome. The discovery of two EST clusters within the deleted region led to the isolation of two noncoding RNA (ncRNA) genes. These were subsequently found differentially expressed in various tumors when compared to their normal tissues. The ncRNA and other highly conserved sequence elements in the deleted region may represent miRNA targets of importance in cancer initiation or progression.

摘要

人类染色体3p12区域的纯合缺失或杂合性丢失(LOH)是肺癌和其他恶性肿瘤的常见特征,这表明该区域存在一个或多个肿瘤抑制基因(TSG)。到目前为止,仅从肺癌和乳腺癌细胞系U2020、NCI H2198及HCC38中缺失的重叠区域克隆到一个基因。根据HUGO命名法,它是DUTT1(在U2020中缺失),也被称为ROBO1、FLJ21882和SAX3。DUTT1是果蝇基因ROBO在人类中的直系同源基因,与神经细胞黏附分子(NCAM)蛋白具有同源性。对肺癌中DUTT1的广泛分析未发现任何突变,这表明该区域的其他基因可能在肺癌的发生和发展中起重要作用。在此,我们报告在小细胞肺癌(SCLC)细胞系GLC20中发现一个新的小的纯合缺失,该缺失位于重叠的关键区域内。利用几个多态性标记和三个重叠的P1噬菌体克隆确定了该缺失区域。纤维荧光原位杂交(Fiber-FISH)实验显示该缺失约为130 kb。比较基因组序列分析发现了在哺乳动物基因组和鸡基因组中高度保守的短序列元件。在缺失区域内发现两个EST簇,从而分离出两个非编码RNA(ncRNA)基因。随后发现,与正常组织相比,这些基因在各种肿瘤中存在差异表达。缺失区域中的ncRNA和其他高度保守的序列元件可能代表在癌症发生或发展中起重要作用的miRNA靶标。

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