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[Transcription factors NF-kB, HIF-1, HIF-2, growth factor VEGF, VEGFR2 and carboanhydrase IX mRNA and protein level in the development of kidney cancer metastasis].[转录因子NF-kB、HIF-1、HIF-2、生长因子VEGF、VEGFR2和碳酸酐酶IX mRNA及蛋白水平在肾癌转移发生过程中的变化]
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LDL cholesterol counteracts the antitumour effect of tyrosine kinase inhibitors against renal cell carcinoma.低密度脂蛋白胆固醇会抵消酪氨酸激酶抑制剂对肾细胞癌的抗肿瘤作用。
Br J Cancer. 2017 Apr 25;116(9):1203-1207. doi: 10.1038/bjc.2017.77. Epub 2017 Mar 28.
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Treatment of locally advanced prostate cancer (Stage T3).局部晚期前列腺癌(T3期)的治疗
Jpn J Clin Oncol. 2017 Mar 1;47(3):257-261. doi: 10.1093/jjco/hyw186.
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Resistance to Targeted Therapies in Renal Cancer: The Importance of Changing the Mechanism of Action.肾癌靶向治疗耐药:改变作用机制的重要性。
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Inhibition of the PI3K/AKT/mTOR Pathway in Solid Tumors.实体瘤中PI3K/AKT/mTOR信号通路的抑制作用
J Clin Oncol. 2016 Nov 1;34(31):3803-3815. doi: 10.1200/JCO.2014.59.0018. Epub 2016 Sep 30.
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[Intracellular signaling mechanisms in thyroid cancer].[甲状腺癌中的细胞内信号传导机制]
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Effect of Target Therapy on the Content of Transcription and Growth Factors, Protein Kinase TOR, and Activity of Intracellular Proteases in Patients with Metastatic Renal Cell Carcinoma.
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The PI3K/Akt Pathway in Tumors of Endocrine Tissues.内分泌组织肿瘤中的PI3K/Akt信号通路
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9
PI3K/Akt/mTOR pathway inhibitors enhance radiosensitivity in radioresistant prostate cancer cells through inducing apoptosis, reducing autophagy, suppressing NHEJ and HR repair pathways.PI3K/Akt/mTOR信号通路抑制剂通过诱导凋亡、减少自噬、抑制非同源末端连接(NHEJ)和同源重组(HR)修复通路来增强耐辐射前列腺癌细胞的放射敏感性。
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The PI3K/AKT/mTOR pathway in breast cancer: targets, trials and biomarkers.乳腺癌中的 PI3K/AKT/mTOR 通路:靶点、试验和生物标志物。
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靶向AKT/m-TOR通路:癌症治疗耐药的生物标志物——AKT/m-TOR通路与癌症治疗耐药

Targeting of the AKT/m-TOR Pathway: Biomarkers of Resistance to Cancer Therapy--
AKT/m-TOR Pathway and Resistance to Cancer Therapy.

作者信息

Spirina Liudmila V, Kondakova Irina V, Tarasenko Natalia V, Slonimskaya Elena M, Usynin Evgeny A, Gorbunov Alexey K, Yurmazov Zahar A, Chigevskaya Svetlana Yu

机构信息

Laboratory of Tumor Biochemistry, Cancer Research Institute, Tomsk National Research Medical Center of the Russian Academy of Sciences, Russia.

Department of Biochemistry and Molecular Biology, Siberian State Medical University, Tomsk, Russia.

出版信息

Zhongguo Fei Ai Za Zhi. 2018 Jan 20;21(1):63-66. doi: 10.3779/j.issn.1009-3419.2018.01.09.

DOI:10.3779/j.issn.1009-3419.2018.01.09
PMID:29357975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5972354/
Abstract

Resistance to cancer therapy continues to be a major limitation for the successful treatment of cancer. There are many published studies on therapy resistance in breast and prostate cancers; however, there are currently no data on molecular markers associated with resistance. The conflicting data were reported regarding the AKT/m-TOR signaling pathway components as markers predicting resistance. The AKT/m-TOR signaling pathway is involved in the development of many human cancers; its activation is related to cell proliferation, angiogenesis, apoptosis, as well as to therapy resistance. Molecular alterations in the AKT/m-TOR signaling pathway provide a platform to identify universal markers associated with the development of resistance to cancer therapy.

摘要

对癌症治疗的耐药性仍然是成功治疗癌症的主要限制因素。关于乳腺癌和前列腺癌治疗耐药性已有许多发表的研究;然而,目前尚无与耐药性相关的分子标志物数据。关于将AKT/m-TOR信号通路成分作为预测耐药性的标志物,已有相互矛盾的数据报道。AKT/m-TOR信号通路参与多种人类癌症的发生发展;其激活与细胞增殖、血管生成、细胞凋亡以及治疗耐药性有关。AKT/m-TOR信号通路中的分子改变为识别与癌症治疗耐药性发展相关的通用标志物提供了一个平台。