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影响前列腺癌的微小RNA:以非裔美国人的前列腺癌为重点

MicroRNAs that affect prostate cancer: emphasis on prostate cancer in African Americans.

作者信息

Jones J, Grizzle W, Wang H, Yates C

机构信息

Department of Biology and Center for Cancer Research, Tuskegee University , Tuskegee, Alabama.

出版信息

Biotech Histochem. 2013 Oct;88(7):410-24. doi: 10.3109/10520295.2013.807069. Epub 2013 Aug 1.

DOI:10.3109/10520295.2013.807069
PMID:23901944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4119086/
Abstract

Although concerted efforts have been directed toward eradicating health disparities in the United States, the disease and mortality rates for African American men still are among the highest in the world. We focus here on the role of microRNAs (miRNAs) in the signaling pathways of androgen receptors and growth factors that promote the progression of prostate cancer to more aggressive disease. We explore also how differential expression of miRNAs contributes to aggressive prostate cancer including that of African Americans.

摘要

尽管美国已齐心协力致力于消除健康差距,但非裔美国男性的疾病和死亡率仍位居世界前列。我们在此聚焦于微小RNA(miRNA)在雄激素受体和生长因子信号通路中的作用,这些信号通路会促使前列腺癌发展为更具侵袭性的疾病。我们还探讨了miRNA的差异表达如何导致侵袭性前列腺癌,包括非裔美国人的侵袭性前列腺癌。

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本文引用的文献

1
MicroRNA-100 regulates IGF1-receptor expression in metastatic pancreatic cancer cells.微小RNA-100调节转移性胰腺癌细胞中IGF1受体的表达。
Biotech Histochem. 2013 Oct;88(7):397-402. doi: 10.3109/10520295.2012.762460. Epub 2013 Feb 4.
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Post-transcriptional processing of genetic information and its relation to cancer.遗传信息的转录后加工及其与癌症的关系。
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miRNA-34b inhibits prostate cancer through demethylation, active chromatin modifications, and AKT pathways.miRNA-34b 通过去甲基化、活性染色质修饰和 AKT 通路抑制前列腺癌。
Clin Cancer Res. 2013 Jan 1;19(1):73-84. doi: 10.1158/1078-0432.CCR-12-2952. Epub 2012 Nov 12.
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Tumor suppressive miR-124 targets androgen receptor and inhibits proliferation of prostate cancer cells.抑瘤 miR-124 靶向雄激素受体并抑制前列腺癌细胞增殖。
Oncogene. 2013 Aug 29;32(35):4130-8. doi: 10.1038/onc.2012.425. Epub 2012 Oct 15.
5
Nuclear Kaiso indicates aggressive prostate cancers and promotes migration and invasiveness of prostate cancer cells.核 Kaiso 提示前列腺癌具有侵袭性,并促进前列腺癌细胞的迁移和侵袭。
Am J Pathol. 2012 Nov;181(5):1836-46. doi: 10.1016/j.ajpath.2012.08.008. Epub 2012 Sep 10.
6
Loss of p63 and its microRNA-205 target results in enhanced cell migration and metastasis in prostate cancer.p63 及其 microRNA-205 靶基因的缺失导致前列腺癌中细胞迁移和转移的增强。
Proc Natl Acad Sci U S A. 2012 Sep 18;109(38):15312-7. doi: 10.1073/pnas.1110977109. Epub 2012 Sep 4.
7
Epigenetic-induced repression of microRNA-205 is associated with MED1 activation and a poorer prognosis in localized prostate cancer.表观遗传诱导的 microRNA-205 抑制与 MED1 激活和局限性前列腺癌不良预后相关。
Oncogene. 2013 Jun 6;32(23):2891-9. doi: 10.1038/onc.2012.300. Epub 2012 Aug 6.
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On the Pro-Metastatic Stress Response to Cancer Therapies: Evidence for a Positive Co-Operation between TIMP-1, HIF-1α, and miR-210.论癌症治疗的促转移应激反应:TIMP-1、HIF-1α和miR-210之间积极协同作用的证据
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Chemoresistance in prostate cancer cells is regulated by miRNAs and Hedgehog pathway.前列腺癌细胞中的化疗耐药性受 miRNAs 和 Hedgehog 通路的调控。
PLoS One. 2012;7(6):e40021. doi: 10.1371/journal.pone.0040021. Epub 2012 Jun 29.
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BMC Urol. 2012 May 29;12:14. doi: 10.1186/1471-2490-12-14.