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[前列腺癌中的危险关联。复发性基因融合的临床和生物学意义]

[Dangerous liaisons in prostate cancer. Clinical and biological implications of recurrent gene fusions].

作者信息

Perner S

机构信息

Institut für Pathologie, Comprehensive Cancer Center, Universitätsklinikum Tübingen, Liebermeisterstr. 8, 72076 Tübingen.

出版信息

Pathologe. 2010 Oct;31 Suppl 2:121-5. doi: 10.1007/s00292-010-1345-7.

DOI:10.1007/s00292-010-1345-7
PMID:20798944
Abstract

Prostate cancer is a common and clinically heterogeneous disease. Understanding the biology of prostate cancer is necessary to best determinate the risk of disease progression and develop novel therapeutic approaches to prevent or slow down disease progression. The recent discovery and subsequent characterization of recurrent gene rearrangements of ETS genes - most frequently ERG - in the majority of prostate cancers is a milestone in translational prostate cancer research. Although multiple molecular alterations have been detected in prostate cancer, a detailed understanding of gene fusion in prostate cancer should help explain the clinical and biologic diversity in addition to providing a rationale for a molecular sub-classification of the disease. This review describes the path from the identification of common ETS gene rearrangements in prostate cancer to possible applications in the treatment of patients, on to the potential scientific implications arising from their discovery.

摘要

前列腺癌是一种常见的且在临床上具有异质性的疾病。了解前列腺癌的生物学特性对于准确确定疾病进展风险以及开发预防或减缓疾病进展的新型治疗方法至关重要。近期在大多数前列腺癌中发现并随后鉴定出ETS基因的复发性基因重排——最常见的是ERG——是前列腺癌转化研究中的一个里程碑。尽管在前列腺癌中已检测到多种分子改变,但对前列腺癌基因融合的详细了解除了可为该疾病的分子亚分类提供理论依据外,还应有助于解释临床和生物学多样性。本综述描述了从在前列腺癌中鉴定常见的ETS基因重排到其在患者治疗中的可能应用,再到因其发现而产生的潜在科学意义的过程。

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[Dangerous liaisons in prostate cancer. Clinical and biological implications of recurrent gene fusions].[前列腺癌中的危险关联。复发性基因融合的临床和生物学意义]
Pathologe. 2010 Oct;31 Suppl 2:121-5. doi: 10.1007/s00292-010-1345-7.
2
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[TMPRSS2-ETS gene fusion in prostate cancer].[前列腺癌中的TMPRSS2-ETS基因融合]
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引用本文的文献

1
ERG rearrangement is associated with prostate cancer-related death in Chinese prostate cancer patients.在中国前列腺癌患者中,ERG重排与前列腺癌相关死亡有关。
PLoS One. 2014 Feb 7;9(2):e84959. doi: 10.1371/journal.pone.0084959. eCollection 2014.

本文引用的文献

1
Relevance of cohort design for studying the frequency of the ERG rearrangement in prostate cancer.研究 ERG 重排在前列腺癌中发生频率的队列设计的相关性。
Histopathology. 2011 Jun;58(7):1028-36. doi: 10.1111/j.1365-2559.2011.03862.x.
2
ERG rearrangement in small cell prostatic and lung cancer.小细胞前列腺癌和肺癌中的 ERG 重排。
Histopathology. 2010 Jun;56(7):937-43. doi: 10.1111/j.1365-2559.2010.03564.x.
3
ERG rearrangement is specific to prostate cancer and does not occur in any other common tumor.ERG 重排是前列腺癌特有的,不会发生在任何其他常见肿瘤中。
Mod Pathol. 2010 Aug;23(8):1061-7. doi: 10.1038/modpathol.2010.87. Epub 2010 May 14.
4
ERG rearrangement metastasis patterns in locally advanced prostate cancer.局部晚期前列腺癌中 ERG 重排的转移模式。
Urology. 2010 Apr;75(4):762-7. doi: 10.1016/j.urology.2009.10.010.
5
ETS gene fusions in prostate cancer: from discovery to daily clinical practice.前列腺癌中的ETS基因融合:从发现到日常临床实践
Eur Urol. 2009 Aug;56(2):275-86. doi: 10.1016/j.eururo.2009.04.036. Epub 2009 Apr 24.
6
Characterization of TMPRSS2-ERG fusion high-grade prostatic intraepithelial neoplasia and potential clinical implications.TMPRSS2-ERG融合性高级别前列腺上皮内瘤变的特征及潜在临床意义
Clin Cancer Res. 2008 Jun 1;14(11):3380-5. doi: 10.1158/1078-0432.CCR-07-5194.
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Estrogen-dependent signaling in a molecularly distinct subclass of aggressive prostate cancer.侵袭性前列腺癌分子特征独特亚类中的雌激素依赖性信号传导
J Natl Cancer Inst. 2008 Jun 4;100(11):815-25. doi: 10.1093/jnci/djn150. Epub 2008 May 27.
8
EML4-ALK fusion lung cancer: a rare acquired event.EML4-ALK融合基因阳性肺癌:一种罕见的获得性事件。
Neoplasia. 2008 Mar;10(3):298-302. doi: 10.1593/neo.07878.
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Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer.磷酸酪氨酸信号的全球调查确定了肺癌中的致癌激酶。
Cell. 2007 Dec 14;131(6):1190-203. doi: 10.1016/j.cell.2007.11.025.
10
TMPRSS2-ERG fusion heterogeneity in multifocal prostate cancer: clinical and biologic implications.多灶性前列腺癌中TMPRSS2-ERG融合的异质性:临床和生物学意义
Urology. 2007 Oct;70(4):630-3. doi: 10.1016/j.urology.2007.08.032.