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本文引用的文献

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Pan-cancer Convergence to a Small-Cell Neuroendocrine Phenotype that Shares Susceptibilities with Hematological Malignancies.泛癌向小细胞神经内分泌表型趋同,与血液系统恶性肿瘤具有共同易感性。
Cancer Cell. 2019 Jul 8;36(1):17-34.e7. doi: 10.1016/j.ccell.2019.06.005.
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Molecular subtypes of small cell lung cancer: a synthesis of human and mouse model data.小细胞肺癌的分子亚型:人类和小鼠模型数据的综合。
Nat Rev Cancer. 2019 May;19(5):289-297. doi: 10.1038/s41568-019-0133-9.
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Impact of ERK5 on the Hallmarks of Cancer.ERK5 对癌症特征的影响。
Int J Mol Sci. 2019 Mar 21;20(6):1426. doi: 10.3390/ijms20061426.
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A chemical biology screen identifies a vulnerability of neuroendocrine cancer cells to SQLE inhibition.一项化学生物学筛选发现了神经内分泌癌细胞对 SQLE 抑制的易感性。
Nat Commun. 2019 Jan 9;10(1):96. doi: 10.1038/s41467-018-07959-4.
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Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2- d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5.ERK5 激酶高选择性、强效(哌啶-4-基)吡啶并[3,2-d]嘧啶类新型在体探针 BAY-885 的发现与鉴定
J Med Chem. 2019 Jan 24;62(2):928-940. doi: 10.1021/acs.jmedchem.8b01606. Epub 2019 Jan 9.
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Statins associate with improved mortality among patients with certain histological subtypes of lung cancer.他汀类药物与某些肺癌组织学亚型患者的死亡率改善相关。
Lung Cancer. 2018 Dec;126:89-96. doi: 10.1016/j.lungcan.2018.10.022. Epub 2018 Oct 25.
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KRAS Suppression-Induced Degradation of MYC Is Antagonized by a MEK5-ERK5 Compensatory Mechanism.KRAS 抑制诱导的 MYC 降解被 MEK5-ERK5 补偿机制拮抗。
Cancer Cell. 2018 Nov 12;34(5):807-822.e7. doi: 10.1016/j.ccell.2018.10.001.
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First-Line Atezolizumab plus Chemotherapy in Extensive-Stage Small-Cell Lung Cancer.阿替利珠单抗联合化疗一线治疗广泛期小细胞肺癌。
N Engl J Med. 2018 Dec 6;379(23):2220-2229. doi: 10.1056/NEJMoa1809064. Epub 2018 Sep 25.
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The Mevalonate Pathway Is a Druggable Target for Vaccine Adjuvant Discovery.甲羟戊酸途径是疫苗佐剂发现的可成药靶点。
Cell. 2018 Nov 1;175(4):1059-1073.e21. doi: 10.1016/j.cell.2018.08.070. Epub 2018 Sep 27.
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A metabolic vulnerability of small-cell lung cancer.小细胞肺癌的一种代谢易损性。
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MEK5-ERK5 激酶轴控制小细胞肺癌中的脂代谢。

The MEK5-ERK5 Kinase Axis Controls Lipid Metabolism in Small-Cell Lung Cancer.

机构信息

Department of Pediatrics, Stanford University, Stanford, California.

Department of Genetics, Stanford University, Stanford, California.

出版信息

Cancer Res. 2020 Mar 15;80(6):1293-1303. doi: 10.1158/0008-5472.CAN-19-1027. Epub 2020 Jan 22.

DOI:10.1158/0008-5472.CAN-19-1027
PMID:31969375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7073279/
Abstract

Small-cell lung cancer (SCLC) is an aggressive form of lung cancer with dismal survival rates. While kinases often play key roles driving tumorigenesis, there are strikingly few kinases known to promote the development of SCLC. Here, we investigated the contribution of the MAPK module MEK5-ERK5 to SCLC growth. MEK5 and ERK5 were required for optimal survival and expansion of SCLC cell lines and . Transcriptomics analyses identified a role for the MEK5-ERK5 axis in the metabolism of SCLC cells, including lipid metabolism. In-depth lipidomics analyses showed that loss of MEK5/ERK5 perturbs several lipid metabolism pathways, including the mevalonate pathway that controls cholesterol synthesis. Notably, depletion of MEK5/ERK5 sensitized SCLC cells to pharmacologic inhibition of the mevalonate pathway by statins. These data identify a new MEK5-ERK5-lipid metabolism axis that promotes the growth of SCLC. SIGNIFICANCE: This study is the first to investigate MEK5 and ERK5 in SCLC, linking the activity of these two kinases to the control of cell survival and lipid metabolism.

摘要

小细胞肺癌(SCLC)是一种侵袭性肺癌,患者生存率极低。尽管激酶通常在推动肿瘤发生中起着关键作用,但已知能够促进 SCLC 发展的激酶却寥寥无几。在这里,我们研究了 MAPK 模块 MEK5-ERK5 对 SCLC 生长的贡献。MEK5 和 ERK5 是 SCLC 细胞系最佳存活和扩增所必需的。转录组学分析确定了 MEK5-ERK5 轴在 SCLC 细胞代谢中的作用,包括脂质代谢。深入的脂质组学分析表明,MEK5/ERK5 的缺失会破坏几种脂质代谢途径,包括控制胆固醇合成的甲羟戊酸途径。值得注意的是,MEK5/ERK5 的耗竭使 SCLC 细胞对他汀类药物抑制甲羟戊酸途径的药理抑制作用更为敏感。这些数据确定了一个新的 MEK5-ERK5-脂质代谢轴,促进了 SCLC 的生长。意义:这项研究首次在 SCLC 中研究了 MEK5 和 ERK5,将这两种激酶的活性与细胞存活和脂质代谢的控制联系起来。