De Cecco Federica, Chellini Lidia, Riccioni Veronica, Paronetto Maria Paola
Department of Movement, Human and Health Sciences, University of Rome Foro Italico, Piazza Lauro de Bosis, 6, 00135 Rome, Italy.
Fondazione Santa Lucia IRCCS, Via del Fosso di Fiorano, 64, 00143 Rome, Italy.
Cancers (Basel). 2025 May 14;17(10):1657. doi: 10.3390/cancers17101657.
Chromosomal rearrangements are implicated in the pathogenesis of several human malignancies, but, concurrently, they also represent targetable opportunities, as exemplified by imatinib (Gleevec), which targets the gene fusion in myeloid leukemia. In prostate cancer, several chromosomal rearrangements have been identified, most of them involving genes, which encode key transcription factors. In this review, we explore the discovery of 5' partners that classify gene fusions into distinct groups based on the prostate specificity and androgen responsiveness. Furthermore, we try to address the relationship between gene fusion status and patient outcomes and discuss the possibility of using prostate-specific targeting of gene fusions in cancer detection, stratification, and treatment.
染色体重排在几种人类恶性肿瘤的发病机制中起作用,但与此同时,它们也代表了可靶向的机会,如伊马替尼(格列卫)靶向髓系白血病中的基因融合所证明的那样。在前列腺癌中,已经鉴定出几种染色体重排,其中大多数涉及编码关键转录因子的基因。在本综述中,我们探索了5'伙伴的发现,这些伙伴根据前列腺特异性和雄激素反应性将基因融合分类为不同的组。此外,我们试图探讨基因融合状态与患者预后之间的关系,并讨论在癌症检测、分层和治疗中使用前列腺特异性靶向基因融合的可能性。