Huang Wei, Waknitz Michelle
Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison 600 Highland Avenue, Madison WI 53792, USA.
Am J Transl Res. 2009 May 25;1(4):341-51.
Chromosomal rearrangements are common genetic alterations in solid tumors and hematologic neoplasias. Recently, gene fusions between erythroblastosis virus E26 transforming sequence (ETS) family of transcription factors and androgen-regulated, prostate-specific TMPRSS2 gene were detected in about 50% of prostate cancers. Further studies have shown a diversity of TMPRSS2:ETS hybrid transcripts and heterogeneity of the fusion genes in multifocal prostate cancer. The role of these gene fusions in prostate carcinogenesis, the protein products associated with the variant fusion transcripts and their association with tumor morphology, stage, and clinical outcomes have also been studied. Additional data have demonstrated ETS gene fusions as a potential biomarker for diagnosing and stratifying prostate cancer patients. The following summarizes these recent advances.
染色体重排是实体瘤和血液系统肿瘤中常见的基因改变。最近,在约50%的前列腺癌中检测到成红细胞增多症病毒E26转化序列(ETS)转录因子家族与雄激素调节的前列腺特异性TMPRSS2基因之间的基因融合。进一步研究表明,多灶性前列腺癌中TMPRSS2:ETS杂合转录本具有多样性,融合基因存在异质性。这些基因融合在前列腺癌发生中的作用、与变异融合转录本相关的蛋白质产物及其与肿瘤形态、分期和临床结局的关联也已得到研究。更多数据表明,ETS基因融合是诊断和分层前列腺癌患者的潜在生物标志物。以下总结了这些最新进展。