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2
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本文引用的文献

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Cancer invasion and metastasis: changing views.癌症侵袭与转移:不断变化的观点
J Pathol. 2008 Feb;214(3):283-93. doi: 10.1002/path.2282.
2
Integrative biology of prostate cancer progression.前列腺癌进展的整合生物学
Annu Rev Pathol. 2006;1:243-71. doi: 10.1146/annurev.pathol.1.110304.100047.
3
Correlation of androgen receptor status, neuroendocrine differentiation and angiogenesis with time-to-biochemical failure after radical prostatectomy in clinically localized prostate cancer.临床局限性前列腺癌根治性前列腺切除术后雄激素受体状态、神经内分泌分化及血管生成与生化复发时间的相关性
Anticancer Res. 2007 Sep-Oct;27(5B):3651-60.
4
Emerging roles of proteases in tumour suppression.蛋白酶在肿瘤抑制中的新作用。
Nat Rev Cancer. 2007 Oct;7(10):800-8. doi: 10.1038/nrc2228.
5
Distribution of 15 human kallikreins in tissues and biological fluids.15种人组织激肽释放酶在组织和生物体液中的分布
Clin Chem. 2007 Aug;53(8):1423-32. doi: 10.1373/clinchem.2007.088104. Epub 2007 Jun 15.
6
Abnormal DNA methylation, epigenetics, and prostate cancer.异常DNA甲基化、表观遗传学与前列腺癌。
Front Biosci. 2007 May 1;12:4254-66. doi: 10.2741/2385.
7
Human tissue kallikreins: a road under construction.人组织激肽释放酶:一条正在建设中的道路。
Clin Chim Acta. 2007 May;381(1):78-84. doi: 10.1016/j.cca.2007.02.023. Epub 2007 Feb 20.
8
Molecular markers for prostate cancer.前列腺癌的分子标志物
Cancer Lett. 2007 Apr 28;249(1):5-13. doi: 10.1016/j.canlet.2006.12.029. Epub 2007 Feb 15.
9
Androgen receptor and prostate cancer.雄激素受体与前列腺癌。
Prostate Cancer Prostatic Dis. 2007;10(2):114-8. doi: 10.1038/sj.pcan.4500936. Epub 2007 Feb 13.
10
Human tissue kallikreins: the cancer biomarker family.人组织激肽释放酶:癌症生物标志物家族
Cancer Lett. 2007 Apr 28;249(1):61-79. doi: 10.1016/j.canlet.2006.12.018. Epub 2007 Jan 31.

KLK15 mRNA 剪接变异体在前列腺癌和良性前列腺增生中的表达分析及研究。

Expression analysis and study of the KLK15 mRNA splice variants in prostate cancer and benign prostatic hyperplasia.

机构信息

Department of Biochemistry and Molecular Biology, University of Athens, Athens, Greece.

出版信息

Cancer Sci. 2010 Mar;101(3):693-9. doi: 10.1111/j.1349-7006.2009.01450.x. Epub 2009 Nov 27.

DOI:10.1111/j.1349-7006.2009.01450.x
PMID:20067463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11158190/
Abstract

Prostate cancer is the most commonly diagnosed malignancy in male populations in the Western world. The KLK15 gene, the newest member of the kallikrein family, is expressed in the prostate gland. The purpose of this study is the expression analysis and the clinical evaluation of the KLK15 mRNA spliced variants in prostate cancer (CaP) and benign prostatic hyperplasia (BPH) patients. Total RNA was isolated from 104 CaP and BPH tissue specimens. After testing the quality of the RNA, cDNA was produced by reverse transcription, and PCR was performed for the amplification of the KLK15 mRNA transcripts. GAPDH and HPRT genes were used as endogenous controls Our data revealed that mRNA spliced variants of KLK15 were differentially expressed in prostate tissue specimens. Analysis of data showed a statistically significant (P < 0.001) increase in the frequency of overexpression of KLK15 transcripts encoding for both the active isoform and for the isoform 3 in CaP compared to BPH samples. Furthermore, KLK15 transcripts were found to be highly expressed in more aggressive tumors (P = 0.017). These results suggest that KLK15 expression analysis could be employed as a valuable tool for the discrimination between BPH and CaP tissue specimens and as an unfavorable prognostic marker for prostate cancer.

摘要

前列腺癌是西方男性人群中最常见的恶性肿瘤。KLK15 基因是激肽释放酶家族的最新成员,在前列腺中表达。本研究的目的是分析 KLK15 mRNA 剪接变异体在前列腺癌(CaP)和良性前列腺增生(BPH)患者中的表达,并进行临床评估。从 104 例 CaP 和 BPH 组织标本中分离总 RNA。在检测 RNA 质量后,通过逆转录生成 cDNA,并进行 PCR 扩增 KLK15 mRNA 转录本。GAPDH 和 HPRT 基因被用作内参。我们的数据显示,KLK15 的 mRNA 剪接变异体在前列腺组织标本中表达不同。数据分析显示,与 BPH 样本相比,编码活性同工型和同工型 3 的 KLK15 转录本的过度表达频率在 CaP 中显著增加(P<0.001)。此外,发现 KLK15 转录本在侵袭性更强的肿瘤中高度表达(P=0.017)。这些结果表明,KLK15 表达分析可作为区分 BPH 和 CaP 组织标本的有用工具,并作为前列腺癌的不利预后标志物。