Fujii Hiroaki, Gabrielson Edward, Takagaki Tetsuya, Ohtsuji Mareki, Ohtsuji Naomi, Hino Okio
Department of Pathology II, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan.
Breast Cancer Res Treat. 2005 May;91(2):103-12. doi: 10.1007/s10549-004-5779-6.
The HIVEP2 gene, located on 6q23-q24, belongs to a family of genes that encodes large zinc fingers containing transcription factor proteins. Although this gene has been implicated in the regulation of immune responses and cellular proliferation, its functions are largely unknown. In the present study, we investigated HIVEP2 gene abnormalities in microdissected breast cancer tissue. For real-time quantitational RT-PCR analysis of paired normal and tumor tissues, mRNA levels were down-regulated to a maximum of 96%. The overall median expression level in breast cancer (33 cases) was significantly lower than that in normal breast tissue (normalized median value of 4.49 versus 17.68; p < 0.0001). Through full-length 5'-RACE (rapid amplification of cDNA ends) analysis, we identified multiple exons in the 5'-untranslated regions with multiple transcriptional start sites, four of which were located in a large CpG island. No tissue- or cancer-specific usage patterns for the transcription start sites were identified by multiplex RT-PCR analysis. Only faint methylation was detected in the 5' region of the island in normal cells and breast cancer tissue, indicating physiological, aging and no tumor-specific methylation. Mutation screening showed only germline polymorphisms. Thus, down-regulation of the HIVEP2 genes frequently occurs and may be one of the genetic events responsible for breast cancer, and their transcription may be regulated by complex mechanisms involving interactions with other factors and/or by other genetic/epigenetic mechanisms.
HIVEP2基因位于6q23 - q24,属于一个基因家族,该家族编码含大锌指结构的转录因子蛋白。尽管该基因与免疫反应调节和细胞增殖有关,但其功能大多未知。在本研究中,我们调查了显微切割的乳腺癌组织中的HIVEP2基因异常情况。对于配对的正常组织和肿瘤组织进行实时定量RT - PCR分析,mRNA水平下调最多达96%。乳腺癌(33例)的总体中位表达水平显著低于正常乳腺组织(标准化中位值分别为4.49和17.68;p < 0.0001)。通过全长5'-RACE(cDNA末端快速扩增)分析,我们在5'-非翻译区鉴定出多个外显子,具有多个转录起始位点,其中四个位于一个大的CpG岛中。多重RT - PCR分析未发现转录起始位点的组织特异性或癌症特异性使用模式。在正常细胞和乳腺癌组织的该岛5'区域仅检测到微弱的甲基化,表明为生理性、衰老相关且无肿瘤特异性甲基化。突变筛查仅显示种系多态性。因此,HIVEP2基因的下调频繁发生,可能是导致乳腺癌的遗传事件之一,其转录可能受涉及与其他因子相互作用的复杂机制和/或其他遗传/表观遗传机制调控。