Dechsukhum C, Ware J L, Ferreira-Gonzalez A, Wilkinson D S, Garrett C T
Department of Pathology, Medical College of Virginia Campus of Virginia Commonwealth University, Richmond, VA 23298-0662, USA.
Mol Diagn. 2000 Jun;5(2):117-28. doi: 10.1007/BF03262030.
The Wilms' tumor 1 (WT1) gene encodes a transcription factor critical in urogenital development. Using a new model of prostate cancer progression that permits comparison of the cellular and molecular properties of increasingly aggressive sublines of simian virus 40 large T-antigen-immortalized human prostate epithelial cells within the same lineage, the role of WT1 in tumorigenesis was investigated.
Using RT-PCR and northern blotting, we identified a novel truncated WT1 transcript in these prostate cancer cell lines. This 2.1-kb transcript consisted of the coding region of the zinc-finger domain of WT1, together with a portion of intron 5 at the 5' end of the transcript. Furthermore, two peptides were detected by western blotting using antibodies to epitopes of the COOH terminus of WT1. Using RT-PCR, the 2.1-kb transcript was also detected in leukemia cell line K562, breast cancer cell line MCF7, and blood samples from patients with acute leukemia.
These novel findings in both cell lines and patient-derived specimens suggest this new WT1 gene alteration has a potential role in the development of new diagnostic assays for some human malignancies.
威尔姆斯瘤1(WT1)基因编码一种在泌尿生殖系统发育中起关键作用的转录因子。利用一种新的前列腺癌进展模型,该模型允许比较同一谱系中猿猴病毒40大T抗原永生化人前列腺上皮细胞中侵袭性不断增加的亚系的细胞和分子特性,研究了WT1在肿瘤发生中的作用。
利用逆转录聚合酶链反应(RT-PCR)和Northern印迹法,我们在这些前列腺癌细胞系中鉴定出一种新的截短型WT1转录本。这种2.1 kb的转录本由WT1锌指结构域的编码区以及转录本5'端内含子5的一部分组成。此外,使用针对WT1羧基末端表位的抗体进行蛋白质印迹法检测到了两种肽。利用RT-PCR,在白血病细胞系K562、乳腺癌细胞系MCF7以及急性白血病患者的血液样本中也检测到了这种2.1 kb的转录本。
在细胞系和患者来源标本中的这些新发现表明,这种新的WT1基因改变在某些人类恶性肿瘤新诊断检测方法的开发中具有潜在作用。