Irshad S, Mahul-Mellier A-L, Kassouf N, Lemarie A, Grimm S
Department of Experimental Medicine and Toxicology, Imperial College London, Hammersmith Campus, London, UK.
Cell Death Differ. 2009 Jun;16(6):890-8. doi: 10.1038/cdd.2009.21. Epub 2009 Mar 13.
We have established a systematic high-throughput screen for genes that cause cell death specifically in transformed tumor cells. In a first round of screening, cDNAs that induce apoptosis in a transformed human cell line are detected. Positive genes are subsequently tested in a synthetic lethal screen in normal cells versus their isogenic counterparts that have been transformed by a particular oncogene. In this way, the organic cation transporter-like 3 (ORCTL3) gene was found to be inactive in normal rat kidney (NRK) cells, but to induce apoptosis in NRK cells transformed by oncogenic H-ras. ORCTL3 also causes cell death in v-src-transformed cells and in various human tumor cell lines but not in normal cells or untransformed cell lines. Although ORCTL3 is a member of the organic cation transporter gene family, our data indicate that this gene induces apoptosis independently of its putative transporter activity. Rather, various lines of evidence suggest that ORCTL3 brings about apoptosis by an endoplasmic reticulum stress-mediated mechanism. Finally, we detected ORCTL3 to be downregulated in human kidney tumors.
我们已经建立了一个系统性的高通量筛选方法,用于筛选那些专门在转化的肿瘤细胞中导致细胞死亡的基因。在第一轮筛选中,检测能在转化的人类细胞系中诱导凋亡的cDNA。随后,在正常细胞与被特定癌基因转化的同基因对应细胞的合成致死筛选中对阳性基因进行测试。通过这种方式,发现有机阳离子转运体样3(ORCTL3)基因在正常大鼠肾(NRK)细胞中无活性,但在被致癌性H-ras转化的NRK细胞中诱导凋亡。ORCTL3在v-src转化的细胞和各种人类肿瘤细胞系中也会导致细胞死亡,但在正常细胞或未转化的细胞系中则不会。尽管ORCTL3是有机阳离子转运体基因家族的成员,但我们的数据表明该基因独立于其假定的转运体活性诱导凋亡。相反,各种证据表明ORCTL3通过内质网应激介导的机制引发凋亡。最后,我们检测到ORCTL在人类肾肿瘤中表达下调。