Nupponen N N, Porkka K, Kakkola L, Tanner M, Persson K, Borg A, Isola J, Visakorpi T
Laboratory of Cancer Genetics, Institute of Medical Technology, University of Tampere, Finland.
Am J Pathol. 1999 Jun;154(6):1777-83. doi: 10.1016/S0002-9440(10)65433-8.
Amplification at the long arm of chromosome 8 occurs in a large fraction of breast and prostate cancers. To clone the target genes for this amplification, we used suppression subtraction hybridization to identify overexpressed genes in the breast cancer cell line SK-Br-3, which harbors amplification at 8q (8q21 and 8q23-q24). A differentially expressed gene identified by SSH, the p40 subunit of eukaryotic translation initiation factor 3 (eIF3), was localized to 8q23 and found to be highly amplified and overexpressed in the breast and prostate cancer cell lines studied. High-level amplification of eIF3-p40 was found in 30% of hormone-refractory prostate tumors and in 18% of untreated primary breast tumors. In the vast majority of the cases, p40 and c-myc were amplified with equal copy numbers. Tumors with higher copy numbers of p40 than c-myc were also found. Expression of p40 mRNA was analyzed with in situ hybridization. The amplification of eIF3-p40 gene was associated with overexpression of its mRNA, as expected for a functional target gene of the amplification. These results imply that genomic aberrations of translation initiation factors, such as eIF3-p40, may contribute to the pathogenesis of breast and prostate cancer.
8号染色体长臂的扩增在大部分乳腺癌和前列腺癌中都有发生。为了克隆这种扩增的靶基因,我们使用抑制性消减杂交技术来鉴定乳腺癌细胞系SK-Br-3中过表达的基因,该细胞系在8q(8q21和8q23-q24)处存在扩增。通过SSH鉴定出的一个差异表达基因,即真核翻译起始因子3(eIF3)的p40亚基,定位于8q23,并且在研究的乳腺癌和前列腺癌细胞系中发现其高度扩增且过表达。在30%的激素难治性前列腺肿瘤和18%的未经治疗的原发性乳腺肿瘤中发现了eIF3-p40的高水平扩增。在绝大多数情况下,p40和c-myc以相同的拷贝数扩增。也发现了p40拷贝数高于c-myc的肿瘤。用原位杂交分析p40 mRNA的表达。正如对扩增的功能性靶基因所预期的那样,eIF3-p40基因的扩增与其mRNA的过表达相关。这些结果表明,翻译起始因子如eIF3-p40的基因组畸变可能与乳腺癌和前列腺癌的发病机制有关。