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将细胞代谢和代谢组学与前列腺癌临床侵袭性的风险分层及潜在治疗途径相联系。

Linking cellular metabolism and metabolomics to risk-stratification of prostate cancer clinical aggressiveness and potential therapeutic pathways.

作者信息

Eidelman Eric, Tripathi Hemantkumar, Fu De-Xue, Siddiqui M Minhaj

机构信息

Division of Urology, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.

出版信息

Transl Androl Urol. 2018 Sep;7(Suppl 4):S490-S497. doi: 10.21037/tau.2018.04.08.

DOI:10.21037/tau.2018.04.08
PMID:30363493
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6178321/
Abstract

Prostate cancer treatment is based on the stratification of disease as low-, intermediate- or high-risk. This stratification has been largely based on anatomic pathology of the disease, as well as through the use of prostate specific antigen (PSA). However, despite this stratification, there remains heterogeneity within the current classification schema. Utilizing a metabolic approach may help to further establish novel biomolecular markers of disease aggressiveness. These markers may eventually be useful in not only the diagnosis of disease but in creating tumor specific targeted therapy for improved clinical outcomes.

摘要

前列腺癌的治疗是基于将疾病分为低风险、中风险或高风险进行分层的。这种分层很大程度上基于疾病的解剖病理学,以及通过使用前列腺特异性抗原(PSA)。然而,尽管有这种分层,当前的分类模式中仍存在异质性。采用代谢方法可能有助于进一步建立疾病侵袭性的新型生物分子标志物。这些标志物最终不仅可能有助于疾病的诊断,还能用于创建肿瘤特异性靶向治疗以改善临床结果。

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本文引用的文献

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An aberrant SREBP-dependent lipogenic program promotes metastatic prostate cancer.异常的 SREBP 依赖性脂肪生成程序促进转移性前列腺癌。
Nat Genet. 2018 Feb;50(2):206-218. doi: 10.1038/s41588-017-0027-2. Epub 2018 Jan 15.
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Clinical Utility and Biologic Implications of Phosphatase and Tensin Homolog (PTEN) and ETS-related Gene (ERG) in Prostate Cancer.磷酸酶和张力蛋白同源物(PTEN)与ETS相关基因(ERG)在前列腺癌中的临床应用及生物学意义
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Stabilization of phosphofructokinase 1 platelet isoform by AKT promotes tumorigenesis.AKT 稳定磷酸果糖激酶 1 血小板同工型促进肿瘤发生。
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Expression of HMGB2 indicates worse survival of patients and is required for the maintenance of Warburg effect in pancreatic cancer.HMGB2的表达表明患者的生存率更低,并且是胰腺癌中维持瓦博格效应所必需的。
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Prostate cancer, PI3K, PTEN and prognosis.前列腺癌、PI3K、PTEN 和预后。
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6
Targeting hexokinase 2 in castration-resistant prostate cancer.靶向去势抵抗性前列腺癌中的己糖激酶2
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Androgen control of lipid metabolism in prostate cancer: novel insights and future applications.雄激素对前列腺癌脂质代谢的调控:新见解与未来应用
Endocr Relat Cancer. 2016 May;23(5):R219-27. doi: 10.1530/ERC-15-0556. Epub 2016 Apr 29.
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The sweet trap in tumors: aerobic glycolysis and potential targets for therapy.肿瘤中的甜蜜陷阱:有氧糖酵解及其潜在治疗靶点
Oncotarget. 2016 Jun 21;7(25):38908-38926. doi: 10.18632/oncotarget.7676.
9
Metabolic targets for potential prostate cancer therapeutics.潜在前列腺癌治疗药物的代谢靶点。
Curr Opin Oncol. 2016 May;28(3):241-7. doi: 10.1097/CCO.0000000000000276.
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Mechanisms of resistance in castration-resistant prostate cancer (CRPC).去势抵抗性前列腺癌(CRPC)的耐药机制。
Transl Androl Urol. 2015 Jun;4(3):365-80. doi: 10.3978/j.issn.2223-4683.2015.05.02.