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Long non-coding RNAs modulate tumor microenvironment to promote metastasis: novel avenue for therapeutic intervention.长链非编码RNA通过调节肿瘤微环境促进转移:治疗干预的新途径。
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本文引用的文献

1
Inactivation of Ink4a/Arf leads to deregulated expression of miRNAs in K-Ras transgenic mouse model of pancreatic cancer.Ink4a/Arf 的失活导致 K-Ras 转基因胰腺癌小鼠模型中 miRNA 的表达失调。
J Cell Physiol. 2012 Oct;227(10):3373-80. doi: 10.1002/jcp.24036.
2
MicroRNA alterations of pancreatic intraepithelial neoplasias.胰腺上皮内瘤变的微小 RNA 改变。
Clin Cancer Res. 2012 Feb 15;18(4):981-92. doi: 10.1158/1078-0432.CCR-11-2347. Epub 2011 Nov 23.
3
MicroRNA-150 directly targets MUC4 and suppresses growth and malignant behavior of pancreatic cancer cells.MicroRNA-150 直接靶向 MUC4,抑制胰腺癌细胞的生长和恶性行为。
Carcinogenesis. 2011 Dec;32(12):1832-9. doi: 10.1093/carcin/bgr223. Epub 2011 Oct 7.
4
Tumor suppressive microRNA-375 regulates lactate dehydrogenase B in maxillary sinus squamous cell carcinoma.抑瘤 microRNA-375 调控上颌窦鳞癌中乳酸脱氢酶 B。
Int J Oncol. 2012 Jan;40(1):185-93. doi: 10.3892/ijo.2011.1196. Epub 2011 Sep 12.
5
Combination of plasma microRNAs with serum CA19-9 for early detection of pancreatic cancer.联合检测血浆 microRNAs 与血清 CA19-9 对胰腺癌的早期诊断价值。
Int J Cancer. 2012 Aug 1;131(3):683-91. doi: 10.1002/ijc.26422. Epub 2011 Nov 19.
6
K-ras(G12V) transformation leads to mitochondrial dysfunction and a metabolic switch from oxidative phosphorylation to glycolysis.K-ras(G12V) 转化导致线粒体功能障碍和代谢从氧化磷酸化向糖酵解的转变。
Cell Res. 2012 Feb;22(2):399-412. doi: 10.1038/cr.2011.145. Epub 2011 Aug 30.
7
MicroRNA-132 targets HB-EGF upon IgE-mediated activation in murine and human mast cells.微小 RNA-132 在 IgE 介导的激活后靶向 HB-EGF 在鼠和人肥大细胞中。
Cell Mol Life Sci. 2012 Mar;69(5):793-808. doi: 10.1007/s00018-011-0786-3. Epub 2011 Aug 19.
8
Oncogenic K-Ras decouples glucose and glutamine metabolism to support cancer cell growth.致癌性 K-Ras 将葡萄糖和谷氨酰胺代谢解偶联,以支持癌细胞生长。
Mol Syst Biol. 2011 Aug 16;7:523. doi: 10.1038/msb.2011.56.
9
Repression of human activation induced cytidine deaminase by miR-93 and miR-155.miR-93 和 miR-155 对人激活诱导胞嘧啶脱氨酶的抑制作用。
BMC Cancer. 2011 Aug 10;11:347. doi: 10.1186/1471-2407-11-347.
10
MicroRNA 144 impairs insulin signaling by inhibiting the expression of insulin receptor substrate 1 in type 2 diabetes mellitus.微小 RNA 144 通过抑制胰岛素受体底物 1 的表达来损害 2 型糖尿病患者的胰岛素信号。
PLoS One. 2011;6(8):e22839. doi: 10.1371/journal.pone.0022839. Epub 2011 Aug 1.

胰腺癌代谢中的 microRNAs。

MicroRNAs in pancreatic cancer metabolism.

机构信息

The Eppley Institute for Cancer and Allied Diseases, University of Nebraska Medical Center, 987696 Nebraska Medical Center, Omaha, NE 68198, USA.

出版信息

Nat Rev Gastroenterol Hepatol. 2012 Apr 17;9(6):334-44. doi: 10.1038/nrgastro.2012.63.

DOI:10.1038/nrgastro.2012.63
PMID:22508159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4045488/
Abstract

Advances in understanding the biology of tumour progression and metastasis have clearly highlighted the importance of aberrant tumour metabolism, which supports not only the energy requirements but also the enormous biosynthetic needs of tumour cells. Such metabolic alterations modulate glucose, amino acid and fatty-acid-dependent metabolite biosynthesis and energy production. Although much progress has been made in understanding the somatic mutations and expression genomics behind these alterations, the regulation of these processes by microRNAs (miRNAs) is only just beginning to be appreciated. This Review focuses on the miRNAs that are potential regulators of the expression of genes whose protein products either directly regulate metabolic machinery or serve as master regulators, indirectly modulating the expression of metabolic enzymes. We focus particularly on miRNAs in pancreatic cancer.

摘要

肿瘤进展和转移生物学研究的进展清楚地强调了肿瘤代谢异常的重要性,它不仅支持肿瘤细胞的能量需求,还支持其巨大的生物合成需求。这些代谢改变调节葡萄糖、氨基酸和脂肪酸依赖性代谢物的生物合成和能量产生。尽管在理解这些改变背后的体细胞突变和表达组学方面已经取得了很大进展,但 miRNA(microRNA)对这些过程的调节才刚刚开始被认识。这篇综述的重点是那些可能调节基因表达的 miRNA,这些基因的蛋白质产物直接调节代谢机制或作为主调控因子,间接调节代谢酶的表达。我们特别关注胰腺癌中的 miRNA。