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细胞周期蛋白依赖性激酶与治疗反应不佳的癌症中的抗氧化基因表达

Cyclin-Dependent Kinase and Antioxidant Gene Expression in Cancers with Poor Therapeutic Response.

作者信息

Scaria George S, Kren Betsy T, Klein Mark A

机构信息

Research Service, Minneapolis VA Health Care System, Minneapolis, MN 55417, USA.

Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Pharmaceuticals (Basel). 2020 Feb 5;13(2):26. doi: 10.3390/ph13020026.

DOI:10.3390/ph13020026
PMID:32033319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7169466/
Abstract

Pancreatic cancer, hepatocellular carcinoma (HCC), and mesothelioma are treatment-refractory cancers, and patients afflicted with these cancers generally have a very poor prognosis. The genomics of these tumors were analyzed as part of The Cancer Genome Atlas (TCGA) project. However, these analyses are an overview and may miss pathway interactions that could be exploited for therapeutic targeting. In this study, the TCGA Pan-Cancer datasets were queried via cBioPortal for correlations among mRNA expression of key genes in the cell cycle and mitochondrial (mt) antioxidant defense pathways. Here we describe these correlations. The results support further evaluation to develop combination treatment strategies that target these two critical pathways in pancreatic cancer, hepatocellular carcinoma, and mesothelioma.

摘要

胰腺癌、肝细胞癌(HCC)和间皮瘤是难治性癌症,罹患这些癌症的患者总体预后通常很差。作为癌症基因组图谱(TCGA)项目的一部分,对这些肿瘤的基因组学进行了分析。然而,这些分析只是一个概述,可能会遗漏可用于治疗靶点的信号通路相互作用。在本研究中,通过cBioPortal查询TCGA泛癌数据集,以寻找细胞周期关键基因的mRNA表达与线粒体(mt)抗氧化防御信号通路之间的相关性。在此我们描述这些相关性。结果支持进一步评估,以制定针对胰腺癌、肝细胞癌和间皮瘤这两个关键信号通路的联合治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/c65b22cb75c2/pharmaceuticals-13-00026-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/7168ced237a5/pharmaceuticals-13-00026-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/c7560913a9fb/pharmaceuticals-13-00026-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/f4849164dd1e/pharmaceuticals-13-00026-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/c65b22cb75c2/pharmaceuticals-13-00026-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/7168ced237a5/pharmaceuticals-13-00026-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/c7560913a9fb/pharmaceuticals-13-00026-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/f4849164dd1e/pharmaceuticals-13-00026-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e934/7169466/c65b22cb75c2/pharmaceuticals-13-00026-g004.jpg

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本文引用的文献

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Chemotherapy for pancreatic cancer.胰腺癌的化疗
Presse Med. 2019 Mar;48(3 Pt 2):e159-e174. doi: 10.1016/j.lpm.2019.02.025. Epub 2019 Mar 15.
2
Transcriptomic analysis of hepatocellular carcinoma reveals molecular features of disease progression and tumor immune biology.肝细胞癌的转录组分析揭示了疾病进展和肿瘤免疫生物学的分子特征。
NPJ Precis Oncol. 2018 Nov 15;2:25. doi: 10.1038/s41698-018-0068-8. eCollection 2018.
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Current chemotherapy strategies in malignant pleural mesothelioma.恶性胸膜间皮瘤的当前化疗策略
Transl Lung Cancer Res. 2018 Oct;7(5):574-583. doi: 10.21037/tlcr.2018.04.10.
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Pembrolizumab in patients with advanced hepatocellular carcinoma previously treated with sorafenib (KEYNOTE-224): a non-randomised, open-label phase 2 trial.帕博利珠单抗治疗索拉非尼治疗后晚期肝细胞癌患者(KEYNOTE-224):一项非随机、开放标签的 2 期试验。
Lancet Oncol. 2018 Jul;19(7):940-952. doi: 10.1016/S1470-2045(18)30351-6. Epub 2018 Jun 3.
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Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial.乐伐替尼与索拉非尼用于不可切除肝细胞癌患者一线治疗的比较:一项随机、III 期非劣效性试验。
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Chemotherapy for hepatocellular carcinoma: current status and future perspectives.肝细胞癌的化疗:现状与未来展望
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Pancreatic Cancer: Molecular Characterization, Clonal Evolution and Cancer Stem Cells.胰腺癌:分子特征、克隆进化与癌症干细胞
Biomedicines. 2017 Nov 18;5(4):65. doi: 10.3390/biomedicines5040065.
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Eradicating Quiescent Tumor Cells by Targeting Mitochondrial Bioenergetics.
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