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早期检测高危前列腺癌的新型实验标志物:细胞间黏附和细胞迁移的作用。

New experimental markers for early detection of high-risk prostate cancer: role of cell-cell adhesion and cell migration.

作者信息

Mol A J M, Geldof A A, Meijer G A, van der Poel H G, van Moorselaar R J A

机构信息

Department of Urology, VU University Medical Center, PO Box 7057, 1007, MB, Amsterdam, The Netherlands.

出版信息

J Cancer Res Clin Oncol. 2007 Oct;133(10):687-95. doi: 10.1007/s00432-007-0235-8. Epub 2007 May 23.

DOI:10.1007/s00432-007-0235-8
PMID:17520286
Abstract

Today's treatment and diagnosis of prostate cancer still exhibit major limitations. The search for new and additional prognostic markers is therefore still an actual field of interest. Potential markers involved in numerous biological processes in the tumor cell have been investigated intensively. For therapeutic interventions it is important to distinguish between harmless and aggressive disease in an early stage. Therefore the subject of this review is limited to markers associated with those functional processes, which discriminate early stage aggressive, metastatic cancer from harmless disease. Important processes in this respect are: altered cell adhesion and cellular migration. E-cadherin, N-cadherin, beta-catenin, integrins, focal adhesion kinase, connexins and matrix metalloproteinases all appear promising biological markers associated with the early stage metastatic process in prostate cancer. Here we discuss their potential to become valid biological markers based on literature data. Thus far, none of these markers proved to be a valid individual marker by itself due to prostate cancer heterogeneity and transient expression. Analyzing a combination of the potential markers discussed in this review is expected to be a better approach toward discriminating high- from low-risk tumors in an early stage of prostate cancer.

摘要

如今,前列腺癌的治疗和诊断仍存在重大局限性。因此,寻找新的及更多的预后标志物仍是当前一个备受关注的领域。人们对肿瘤细胞中众多生物过程所涉及的潜在标志物进行了深入研究。对于治疗干预而言,在早期区分无害疾病和侵袭性疾病至关重要。因此,本综述的主题仅限于与那些能够将早期侵袭性转移性癌症与无害疾病区分开来的功能过程相关的标志物。这方面的重要过程包括:细胞黏附改变和细胞迁移。E-钙黏蛋白、N-钙黏蛋白、β-连环蛋白、整合素、黏着斑激酶、连接蛋白和基质金属蛋白酶似乎都是与前列腺癌早期转移过程相关的有前景的生物标志物。在此,我们根据文献数据讨论它们成为有效生物标志物的潜力。迄今为止,由于前列腺癌的异质性和瞬时表达,这些标志物中没有一个本身被证明是有效的单个标志物。分析本综述中讨论的潜在标志物的组合有望成为在前列腺癌早期区分高风险和低风险肿瘤的更好方法。

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本文引用的文献

1
E-cadherin promoter polymorphisms are not associated with the aggressiveness of prostate cancer in Caucasian patients.E-钙黏蛋白启动子多态性与白种人前列腺癌患者的侵袭性无关。
Urol Oncol. 2006 Nov-Dec;24(6):496-502. doi: 10.1016/j.urolonc.2006.02.018.
2
The impact of cell adhesion changes on proliferation and survival during prostate cancer development and progression.细胞黏附变化对前列腺癌发生发展过程中增殖和存活的影响。
J Cell Biochem. 2006 Oct 1;99(2):345-61. doi: 10.1002/jcb.20934.
3
Active surveillance with selective delayed intervention for favorable risk prostate cancer.
The role of adhesion molecules as biomarkers for the aggressive prostate cancer phenotype.
黏附分子作为侵袭性前列腺癌表型生物标志物的作用。
PLoS One. 2013 Dec 16;8(12):e81666. doi: 10.1371/journal.pone.0081666. eCollection 2013.
4
Isolated, disseminated and circulating tumour cells in prostate cancer.前列腺癌中的孤立、播散和循环肿瘤细胞。
Nat Rev Urol. 2012 Aug;9(8):448-63. doi: 10.1038/nrurol.2012.136. Epub 2012 Jul 10.
5
Identification of androgen-regulated genes in human prostate.鉴定人前列腺中的雄激素调节基因。
Mol Med Rep. 2012 Sep;6(3):466-72. doi: 10.3892/mmr.2012.956. Epub 2012 Jun 19.
6
The role of connexins in prostate cancer promotion and progression.缝隙连接蛋白在前列腺癌促进和进展中的作用。
Nat Rev Urol. 2012 Feb 21;9(5):274-82. doi: 10.1038/nrurol.2012.14.
7
Steps in prostate cancer progression that lead to bone metastasis.导致前列腺癌骨转移的进展步骤。
Int J Cancer. 2011 Jun 1;128(11):2545-61. doi: 10.1002/ijc.26024. Epub 2011 Mar 28.
8
Therapeutic targeting of the prostate cancer microenvironment.治疗性靶向前列腺癌微环境。
Nat Rev Urol. 2010 Sep;7(9):494-509. doi: 10.1038/nrurol.2010.134.
9
Expression and prognostic significance of focal adhesion kinase in hepatocellular carcinoma.肝癌中黏着斑激酶的表达及其预后意义。
J Cancer Res Clin Oncol. 2010 Oct;136(10):1489-96. doi: 10.1007/s00432-010-0806-y. Epub 2010 Feb 12.
10
Detecting disease associated modules and prioritizing active genes based on high throughput data.基于高通量数据检测疾病相关模块并对活性基因进行优先级排序。
BMC Bioinformatics. 2010 Jan 13;11:26. doi: 10.1186/1471-2105-11-26.
对低风险前列腺癌进行主动监测并选择性延迟干预。
Urol Oncol. 2006 Jan-Feb;24(1):46-50. doi: 10.1016/j.urolonc.2005.07.002.
4
E-cadherin polymorphisms and haplotypes influence risk for prostate cancer.E-钙黏蛋白多态性和单倍型影响前列腺癌风险。
Prostate. 2006 Apr 1;66(5):546-56. doi: 10.1002/pros.20374.
5
Aberrant expression of E-cadherin and beta-catenin in human prostate cancer.E-钙黏蛋白和β-连环蛋白在人类前列腺癌中的异常表达。
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6
N-cadherin switching occurs in high Gleason grade prostate cancer.N-钙黏蛋白转换发生在高Gleason分级的前列腺癌中。
Prostate. 2006 Feb 1;66(2):193-9. doi: 10.1002/pros.20334.
7
Changes in gap junctional connexin isoforms during prostate cancer progression.
Prostate. 2006 Jan 1;66(1):19-31. doi: 10.1002/pros.20317.
8
Molecular requirements for epithelial-mesenchymal transition during tumor progression.肿瘤进展过程中上皮-间质转化的分子要求
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9
Wnt signalling and prostate cancer.Wnt信号通路与前列腺癌。
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Mechanisms of cancer cell invasion.癌细胞侵袭的机制。
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