Zendman A J, Cornelissen I M, Weidle U H, Ruiter D J, van Muijen G N
Department of Pathology, University Hospital, Nijmegen, The Netherlands.
Cancer Res. 1999 Dec 15;59(24):6223-9.
To identify new genes that may contribute to the metastatic pathway of neoplastic cells, we compared mRNA expression of the parental human melanoma cell line 1F6 and its metastatic variant 1F6m using mRNA differential display. We isolated a cDNA clone that was exclusively expressed in 1F6m. Northern blot analysis on a broader panel of human melanoma cell lines with different metastatic capacity following s.c. inoculation into nude mice demonstrated that the gene was expressed only in the most aggressive, highly metastatic cell lines, giving a band of 0.5 kb. The isolated full length cDNA clone showed an open reading frame of 97 amino acids. To study the subcellular localization of the gene product, COS-1 cells were transfected with cDNA of the gene fused to eGFP. We found the fusion protein to be exclusively present in the nucleus. A computer search showed strong homology with human genomic clones all localized on chromosome X (Xq26.3-Xq27.1) and with several expressed sequence tags, all from testis. Localization of the gene on chromosome X was confirmed by genomic PCR on a panel of human chromosome-specific rodent/human hybrid cell lines. Northern blotting and reverse transcription-PCR on 17 different normal human tissue samples showed that the gene was only expressed in normal testis. Reverse transcription-PCR on a great number of different human tumor cell lines showed expression in 25-30% of the melanoma and bladder carcinoma cell lines. Only 2 of 29 other tumor cell lines were positive. Nested PCR analysis of a series of fresh human melanocytic tumors demonstrated expression in 7 of 10 melanomas tested. No expression was seen in benign melanocytic tumors. In addition to melanoma, some malignant tumors from other histological types were also found to be positive. Based on these data, we conclude that the described gene, CTp11 (cancer/testis-associated protein of 11 kDa), is a novel member of the family of cancer/testis antigens.
为了鉴定可能参与肿瘤细胞转移途径的新基因,我们使用mRNA差异显示技术比较了亲本人类黑色素瘤细胞系1F6及其转移变体1F6m的mRNA表达。我们分离出一个仅在1F6m中表达的cDNA克隆。对一系列具有不同转移能力的人类黑色素瘤细胞系进行皮下接种到裸鼠后进行Northern印迹分析,结果表明该基因仅在最具侵袭性、高转移性的细胞系中表达,呈现出一条0.5 kb的条带。分离出的全长cDNA克隆显示有一个97个氨基酸的开放阅读框。为了研究该基因产物的亚细胞定位,用与eGFP融合的该基因的cDNA转染COS-1细胞。我们发现融合蛋白仅存在于细胞核中。计算机搜索显示与所有定位于X染色体(Xq26.3 - Xq27.1)的人类基因组克隆以及几个均来自睾丸的表达序列标签有很强的同源性。通过对一组人类染色体特异性啮齿动物/人类杂交细胞系进行基因组PCR,证实了该基因在X染色体上的定位。对17种不同的正常人类组织样本进行Northern印迹和逆转录PCR分析表明,该基因仅在正常睾丸中表达。对大量不同的人类肿瘤细胞系进行逆转录PCR分析表明,在25% - 30%的黑色素瘤和膀胱癌细胞系中有表达。其他29种肿瘤细胞系中只有2种呈阳性。对一系列新鲜人类黑素细胞肿瘤进行巢式PCR分析表明,在10个检测的黑色素瘤中有7个有表达。在良性黑素细胞肿瘤中未观察到表达。除黑色素瘤外,还发现一些其他组织学类型的恶性肿瘤也呈阳性。基于这些数据,我们得出结论,所描述的基因CTp11(11 kDa的癌/睾丸相关蛋白)是癌/睾丸抗原家族的一个新成员。