Hamaguchi Masaaki, Meth Jennifer L, von Klitzing Christine, Wei Wen, Esposito Diane, Rodgers Linda, Walsh Tom, Welcsh Piri, King Mary-Claire, Wigler Michael H
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA.
Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13647-52. doi: 10.1073/pnas.212516099. Epub 2002 Oct 7.
A previously uncharacterized gene, DBC2 (deleted in breast cancer), was cloned from a homozygously deleted region at human chromosome 8p21. DBC2 contains a highly conserved RAS domain and two putative protein interacting domains. Our analyses indicate that DBC2 is the best candidate tumor suppressor gene from this region. It lies within the epicenter of the deletions and is homozygously deleted in 3.5% (7/200) of breast tumors. Mutation analysis of DBC2 led to discovery of two instances of somatic missense mutations in breast tumor specimens, whereas no missense mutations were found in other candidates from the region. Unlike other genes in the region, expression of DBC2 is often extinguished in breast cancer cells or tissues. Moreover, our functional analysis revealed that DBC2 expression in breast cancer cells lacking DBC2 transcripts causes growth inhibition. By contrast, expression of a somatic mutant discovered in a breast cancer specimen does not suppress the growth of breast cancer cells.
一个先前未被鉴定的基因,DBC2(乳腺癌缺失基因),是从人类染色体8p21的一个纯合缺失区域克隆出来的。DBC2包含一个高度保守的RAS结构域和两个假定的蛋白质相互作用结构域。我们的分析表明,DBC2是该区域最佳的候选肿瘤抑制基因。它位于缺失区域的中心,在3.5%(7/200)的乳腺肿瘤中发生纯合缺失。对DBC2的突变分析导致在乳腺肿瘤标本中发现了两例体细胞错义突变,而在该区域的其他候选基因中未发现错义突变。与该区域的其他基因不同,DBC2在乳腺癌细胞或组织中的表达常常消失。此外,我们的功能分析表明,在缺乏DBC2转录本的乳腺癌细胞中表达DBC2会导致生长抑制。相比之下,在一个乳腺癌标本中发现的体细胞突变体的表达并不能抑制乳腺癌细胞的生长。