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前列腺癌中的ETS基因融合:从发现到日常临床实践

ETS gene fusions in prostate cancer: from discovery to daily clinical practice.

作者信息

Tomlins Scott A, Bjartell Anders, Chinnaiyan Arul M, Jenster Guido, Nam Robert K, Rubin Mark A, Schalken Jack A

机构信息

Michigan Center for Translational Pathology, Department of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.

出版信息

Eur Urol. 2009 Aug;56(2):275-86. doi: 10.1016/j.eururo.2009.04.036. Epub 2009 Apr 24.

Abstract

CONTEXT

In 2005, fusions between the androgen-regulated transmembrane protease serine 2 gene, TMPRSS2, and E twenty-six (ETS) transcription factors were discovered in prostate cancer.

OBJECTIVE

To review advances in our understanding of ETS gene fusions, focusing on challenges affecting translation to clinical application.

EVIDENCE ACQUISITION

The PubMed database was searched for reports on ETS fusions in prostate cancer.

EVIDENCE SYNTHESIS

Since the discovery of ETS fusions, novel 5' and 3' fusion partners and multiple splice isoforms have been reported. The most common fusion, TMPRSS2:ERG, is present in approximately 50% of prostate-specific antigen (PSA)-screened localized prostate cancers and in 15-35% of population-based cohorts. ETS fusions can be detected noninvasively in the urine of men with prostate cancer, with a specificity rate in PSA-screened cohorts of >90%. Reports from untreated population-based cohorts suggest an association between ETS fusions and cancer-specific death and metastatic spread. In retrospective prostatectomy cohorts, conflicting results have been published regarding associations between ETS fusions and cancer aggressiveness. In addition to serving as a potential biomarker, tissue and functional studies suggest a specific role for ETS fusions in the transition to carcinoma. Finally, recent results suggest that the 5' and 3' ends of ETS fusions as well as downstream targets may be targeted therapeutically.

CONCLUSIONS

Recent studies suggest that the first clinical applications of ETS fusions are likely to be in noninvasive detection of prostate cancer and in aiding with difficult diagnostic cases. Additional studies are needed to clarify the association between gene fusions and cancer aggressiveness, particularly those studies that take into account the multifocal and heterogeneous nature of localized prostate cancer. Multiple promising strategies have been identified to potentially target ETS fusions. Together, these results suggest that ETS fusions will affect multiple aspects of prostate cancer diagnosis and management.

摘要

背景

2005年,在前列腺癌中发现雄激素调节的跨膜蛋白酶丝氨酸2基因(TMPRSS2)与E26(ETS)转录因子之间发生融合。

目的

综述我们对ETS基因融合认识的进展,重点关注影响其临床应用转化的挑战。

证据获取

检索PubMed数据库中关于前列腺癌中ETS融合的报道。

证据综合

自发现ETS融合以来,已报道了新的5'和3'融合伙伴以及多种剪接异构体。最常见的融合形式TMPRSS2:ERG存在于约50%经前列腺特异性抗原(PSA)筛查的局限性前列腺癌以及15%-35%基于人群的队列中。ETS融合可在前列腺癌患者的尿液中无创检测到,在PSA筛查队列中的特异率>90%。来自未经治疗的基于人群队列的报道表明ETS融合与癌症特异性死亡和转移扩散之间存在关联。在回顾性前列腺切除队列中,关于ETS融合与癌症侵袭性之间的关联已发表了相互矛盾的结果。除了作为潜在的生物标志物外,组织和功能研究表明ETS融合在向癌转化过程中具有特定作用。最后,近期结果表明ETS融合的5'和3'末端以及下游靶点可能成为治疗靶点。

结论

近期研究表明,ETS融合的首个临床应用可能在于前列腺癌的无创检测以及辅助诊断疑难病例。需要更多研究来阐明基因融合与癌症侵袭性之间的关联,特别是那些考虑到局限性前列腺癌多灶性和异质性的研究。已确定了多种有前景的策略来潜在靶向ETS融合。总之,这些结果表明ETS融合将影响前列腺癌诊断和管理的多个方面。

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