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Diagnosing Lung Cancers through Examination of Micro-RNA Biomarkers in Blood, Plasma, Serum and Sputum: A Review and Summary of Current Literature.通过检测血液、血浆、血清和痰液中的微小RNA生物标志物诊断肺癌:当前文献综述与总结
Int J Mol Sci. 2016 Apr 1;17(4):494. doi: 10.3390/ijms17040494.
2
Everolimus-induced epithelial to mesenchymal transition (EMT) in bronchial/pulmonary cells: when the dosage does matter in transplantation.依维莫司诱导支气管/肺细胞上皮-间质转化(EMT):移植中剂量何时起关键作用。
J Nephrol. 2016 Dec;29(6):881-891. doi: 10.1007/s40620-016-0295-4. Epub 2016 Mar 29.
3
Sirolimus induces apoptosis and reverses multidrug resistance in human osteosarcoma cells in vitro via increasing microRNA-34b expression.西罗莫司通过增加微小RNA-34b的表达在体外诱导人骨肉瘤细胞凋亡并逆转多药耐药性。
Acta Pharmacol Sin. 2016 Apr;37(4):519-29. doi: 10.1038/aps.2015.153. Epub 2016 Feb 29.
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MicroRNA-147 suppresses proliferation, invasion and migration through the AKT/mTOR signaling pathway in breast cancer.微小RNA-147通过AKT/mTOR信号通路抑制乳腺癌的增殖、侵袭和迁移。
Oncol Lett. 2016 Jan;11(1):405-410. doi: 10.3892/ol.2015.3842. Epub 2015 Oct 29.
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Radiation-induced miR-208a increases the proliferation and radioresistance by targeting p21 in human lung cancer cells.辐射诱导的miR-208a通过靶向人肺癌细胞中的p21来增加细胞增殖和放射抗性。
J Exp Clin Cancer Res. 2016 Jan 12;35:7. doi: 10.1186/s13046-016-0285-3.
6
Anti-Tumor Activity of Yuanhuacine by Regulating AMPK/mTOR Signaling Pathway and Actin Cytoskeleton Organization in Non-Small Cell Lung Cancer Cells.芫花酯甲通过调控非小细胞肺癌细胞中的AMPK/mTOR信号通路及肌动蛋白细胞骨架组织发挥抗肿瘤活性
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Sci Rep. 2015 Dec 7;5:17499. doi: 10.1038/srep17499.
8
mTOR inhibitor-induced interstitial lung disease in cancer patients: Comprehensive review and a practical management algorithm.mTOR 抑制剂所致癌症患者的间质性肺病:全面综述及实用管理算法。
Int J Cancer. 2016 May 15;138(10):2312-21. doi: 10.1002/ijc.29887. Epub 2015 Oct 27.
9
p53 Deletion or Hotspot Mutations Enhance mTORC1 Activity by Altering Lysosomal Dynamics of TSC2 and Rheb.p53基因缺失或热点突变通过改变结节性硬化症复合物2(TSC2)和小G蛋白Rheb的溶酶体动力学来增强mTORC1活性。
Mol Cancer Res. 2016 Jan;14(1):66-77. doi: 10.1158/1541-7786.MCR-15-0159. Epub 2015 Sep 18.
10
MicroRNAs in lung diseases: Recent findings and their pathophysiological implications.肺部疾病中的微小RNA:最新发现及其病理生理学意义
Pulm Pharmacol Ther. 2015 Oct;34:55-63. doi: 10.1016/j.pupt.2015.08.007. Epub 2015 Aug 28.

靶向雷帕霉素在肺癌中的哺乳动物靶点

Targeting the Mammalian Target of Rapamycin in Lung Cancer.

作者信息

Vicary Glenn W, Roman Jesse

机构信息

Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, Kentucky.

Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, Kentucky; Division of Pulmonary, Critical Care, and Sleep Disorders Medicine, Department of Medicine, University of Louisville School of Medicine, Louisville, Kentucky; Lousiville Veterans Affairs Medical Center, Louisville, Kentucky.

出版信息

Am J Med Sci. 2016 Nov;352(5):507-516. doi: 10.1016/j.amjms.2016.08.014. Epub 2016 Aug 21.

DOI:10.1016/j.amjms.2016.08.014
PMID:27865299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5384343/
Abstract

Lung cancer is the leading cause of cancer death worldwide. Despite advances in its prevention and management, the prognosis of patients with lung cancer remains poor. Therefore, much attention is being given to factors that contribute to the development of this disease, the mechanisms that drive oncogenesis and tumor progression and the search for novel targets that could lead to the development of more effective treatments. One cellular pathway implicated in lung cancer development and progression is that of the mammalian target of rapamycin. Studies involving human tissues have linked lung cancer with abnormalities in this pathway. Furthermore, studies in vitro and in vivo using animal models of lung cancer reveal that targeting this pathway might represent an effective means of treating this disease. As a result, there is significant effort invested in the development of drugs targeting mammalian target of rapamycin and related pathways in the clinical setting.

摘要

肺癌是全球癌症死亡的主要原因。尽管在其预防和治疗方面取得了进展,但肺癌患者的预后仍然很差。因此,人们非常关注导致这种疾病发生的因素、驱动肿瘤发生和肿瘤进展的机制,以及寻找能够带来更有效治疗方法的新靶点。一条与肺癌发生和进展相关的细胞通路是雷帕霉素哺乳动物靶点通路。涉及人体组织的研究已将肺癌与该通路的异常联系起来。此外,使用肺癌动物模型进行的体外和体内研究表明,针对该通路可能是治疗这种疾病的有效手段。因此,在临床环境中,人们投入了大量精力来开发针对雷帕霉素哺乳动物靶点及相关通路的药物。