Marmé Alexander, Zimmermann Hans-Peter, Moldenhauer Gerhard, Schorpp-Kistner Marina, Müller Claudia, Keberlein Olga, Giersch Antje, Kretschmer Jürgen, Seib Brigitte, Spiess Eberhard, Hunziker Andreas, Merchán Faustino, Möller Peter, Hahn Uwe, Kurek Raffael, Marmé Frederik, Bastert Gunther, Wallwiener Diethelm, Ponstingl Herwig
Department of Obstetrics and Gynecology, University of Heidelberg, Heidelberg, Germany.
Int J Cancer. 2008 Nov 1;123(9):2048-56. doi: 10.1002/ijc.23763.
In a study on gene deregulation in ovarian carcinoma we found a mRNA coding for a 350 kDa protein, Drop1, to be downregulated 20- to 180-fold in the majority of ovarian and mammary carcinomas. The mRNA is encoded by a set of exons in the 5' region of the SYNE1 gene. Immunohistochemical staining for Drop1 protein by a specific monoclonal antibody corresponds to the pattern seen for the mRNA. cDNA arrays of matched pairs of tumor and normal tissue and in situ hybridizations confirmed the drastic loss of Drop1 mRNA as a common feature in uterus, cervix, kidney, lung, thyroid and pancreas carcinomas, already at early tumor stages and in all metastases. Two-hybrid studies suggest a role of this deficiency in the malignant progression of epithelial tumors.
在一项关于卵巢癌基因失调的研究中,我们发现一种编码350 kDa蛋白质Drop1的mRNA,在大多数卵巢癌和乳腺癌中下调了20至180倍。该mRNA由SYNE1基因5'区域的一组外显子编码。用特异性单克隆抗体对Drop1蛋白进行免疫组织化学染色,结果与mRNA的情况相符。肿瘤与正常组织配对的cDNA阵列以及原位杂交证实,Drop1 mRNA的显著缺失是子宫癌、宫颈癌、肾癌、肺癌、甲状腺癌和胰腺癌的共同特征,在肿瘤早期阶段以及所有转移灶中均已出现。双杂交研究表明,这种缺陷在上皮肿瘤的恶性进展中起作用。