Kuehl W M, Brents L A, Chesi M, Huppi K, Bergsagel P L
NCI-Navy Medical Oncology Branch, Bethesda, MD 20889, USA.
Curr Top Microbiol Immunol. 1997;224:277-82. doi: 10.1007/978-3-642-60801-8_29.
Translocation of c-myc to IgH switch regions, or less frequently to one of the IgL loci, is essentially an invariant event in murine plasmacytomas. This results in dysregulation of c-myc, manifested by selective expression of the translocated allele. Human multiple myeloma (MM) has a similarly high incidence of translocations involving IgH switch regions, but c-myc is infrequently involved as a partner in these translocations. However, in screening a panel of 20 MM cell lines, we identified six lines containing two genetically distinguishable c-myc alleles. For these six informative lines (and the corresponding tumor for one line) there is selective expression of one c-myc allele despite the apparent absence of translocation, DNA rearrangement, or amplification involving c-myc. This result suggests frequent tumor specific cis-dysregulation of c-myc in MM by a presently unknown mechanism.
在鼠浆细胞瘤中,c-myc易位至IgH转换区,或较少见地易位至其中一个IgL基因座,本质上是一个不变的事件。这导致c-myc失调,表现为易位等位基因的选择性表达。人类多发性骨髓瘤(MM)同样有很高比例的涉及IgH转换区的易位,但在这些易位中c-myc很少作为伙伴基因参与。然而,在对一组20个MM细胞系进行筛查时,我们鉴定出6个细胞系含有两个基因上可区分的c-myc等位基因。对于这6个信息丰富的细胞系(以及其中一个细胞系对应的肿瘤),尽管明显不存在涉及c-myc的易位、DNA重排或扩增,但仍有一个c-myc等位基因的选择性表达。这一结果表明,MM中c-myc频繁发生肿瘤特异性顺式失调,其机制目前尚不清楚。