KCNK levels are prognostic and diagnostic markers for hepatocellular carcinoma
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Bo Liu | Jie Ren | Peng Zhang | Yadi Liao | Wen-Chao Li | Zhi-Yong Xiong | Pin-Zhu Huang | Yang-Jing Liao | Quan-Xi Li | Zhi-Cheng Yao | Ya-Di Liao | Shi-Lei Xu | Hui Zhou | Qing-Liang Wang | He Huang | Peng Zhang | Ji-Zong Lin | Kun-Peng Hu | Kunpeng Hu | Bo Liu | Hui Zhou | Pin-zhu Huang | Jizong Lin | Zhiyong Xiong | He Huang | Zhichao Yao | Wenchao Li | Qing-Liang Wang | Yangjing Liao | Quan-Xi Li | Shicheng Xu | Jie Ren
[1] R. Lifton,et al. Macrolides selectively inhibit mutant KCNJ5 potassium channels that cause aldosterone-producing adenoma , 2017, The Journal of clinical investigation.
[2] K. O’Shaughnessy,et al. Both TASK-3 and TREK-1 two-pore loop K channels are expressed in H295R cells and modulate their membrane potential and aldosterone secretion. , 2008, American journal of physiology. Endocrinology and metabolism.
[3] M. Wigler,et al. Genomic amplification and oncogenic properties of the KCNK9 potassium channel gene. , 2003, Cancer cell.
[4] Dongling Yang,et al. FXYD6: a novel therapeutic target toward hepatocellular carcinoma , 2014, Protein & Cell.
[5] Detlef Bockenhauer,et al. Potassium leak channels and the KCNK family of two-p-domain subunits , 2001, Nature Reviews Neuroscience.
[6] Jun Liu,et al. Identification of Crucial Genes Associated With Immune Cell Infiltration in Hepatocellular Carcinoma by Weighted Gene Co-expression Network Analysis , 2020, Frontiers in Genetics.
[7] H. Kwan,et al. Blockage of voltage-gated K+ channels inhibits adhesion and proliferation of hepatocarcinoma cells. , 2003, International journal of molecular medicine.
[8] A. Jemal,et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries , 2018, CA: a cancer journal for clinicians.
[9] G. Gores,et al. Hepatocellular carcinoma: clinical frontiers and perspectives , 2014, Gut.
[10] D. Lotshaw. Biophysical, pharmacological, and functional characteristics of cloned and native mammalian two-pore domain K+ channels , 2007, Cell Biochemistry and Biophysics.
[11] E. Honoré,et al. The neuronal background K2P channels: focus on TREK1 , 2007, Nature Reviews Neuroscience.
[12] Q. Ding,et al. Transmembrane channel-like protein 8 as a potential biomarker for poor prognosis of hepatocellular carcinoma. , 2017, Molecular and clinical oncology.
[13] M. Lazdunski,et al. Genomic and functional characteristics of novel human pancreatic 2P domain K(+) channels. , 2001, Biochemical and biophysical research communications.
[14] L. Csernoch,et al. Mitochondrial expression of the two-pore domain TASK-3 channels in malignantly transformed and non-malignant human cells , 2008, Virchows Archiv.
[15] Hao Chen,et al. The potassium channel KCa3.1 promotes cell proliferation by activating SKP2 and metastasis through the EMT pathway in hepatocellular carcinoma , 2019, International journal of cancer.
[16] Mapping of human potassium channel genes TREK-1 (KCNK2) and TASK (KCNK3) to chromosomes 1q41 and 2p23. , 1998, Genomics.
[17] Chao Wu,et al. ASIC1a mediates the drug resistance of human hepatocellular carcinoma via the Ca2+/PI3-kinase/AKT signaling pathway , 2016, Laboratory Investigation.
[18] P. Stanfield,et al. TASK-5, a novel member of the tandem pore K+ channel family , 2001, Pflügers Archiv.
[19] C. Cordon-Cardo,et al. TREK-1 is a novel molecular target in prostate cancer. , 2008, Cancer research.
[20] Y. Wan,et al. Decreased abundance of TRESK two-pore domain potassium channels in sensory neurons underlies the pain associated with bone metastasis , 2018, Science Signaling.
[21] John P. Overington,et al. How many drug targets are there? , 2006, Nature Reviews Drug Discovery.
[22] Chad J. Creighton,et al. UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses , 2017, Neoplasia.
[23] Fei Zou,et al. ATP-sensitive potassium channels control glioma cells proliferation by regulating ERK activity. , 2009, Carcinogenesis.
[24] A. Villanueva,et al. Liver capsule: Molecular‐based signatures in hepatocellular carcinoma , 2016, Hepatology.
[25] P. Purhonen,et al. Structure of potassium channels , 2015, Cellular and Molecular Life Sciences.
[26] Lewis J. Watson,et al. The two-pore domain potassium channel TREK-1 mediates cardiac fibrosis and diastolic dysfunction , 2018, The Journal of clinical investigation.
[27] M. Borggrefe,et al. Upregulation of K2P3.1 K+ Current Causes Action Potential Shortening in Patients With Chronic Atrial Fibrillation , 2015, Circulation.
[28] Y. Miao,et al. ALKBH5 Inhibits Pancreatic Cancer Motility by Decreasing Long Non-Coding RNA KCNK15-AS1 Methylation , 2018, Cellular Physiology and Biochemistry.
[29] Péter Enyedi,et al. Molecular Background of Leak K (cid:1) Currents: Two-Pore Domain Potassium Channels , 2010 .
[30] Mansoor Abdul,et al. Expression and activity of potassium ion channels in human prostate cancer. , 2002, Cancer letters.
[31] L. Pardo,et al. Overexpression of Eag1 potassium channels in clinical tumours , 2006, Molecular Cancer.
[32] D. Minor,et al. K2P2.1(TREK-1):activator complexes reveal a cryptic selectivity filter binding site , 2017, Nature.
[33] Wei Liu,et al. Hypermethylated KCNQ1 acts as a tumor suppressor in hepatocellular carcinoma. , 2018, Biochemical and biophysical research communications.
[34] S. Goldstein,et al. ORK1, a potassium-selective leak channel with two pore domains cloned from Drosophila melanogaster by expression in Saccharomyces cerevisiae. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[35] Donghee Kim,et al. TASK-3, a New Member of the Tandem Pore K+ Channel Family* , 2000, The Journal of Biological Chemistry.
[36] H. Sowter,et al. Expression and effects of modulation of the K2P potassium channels TREK-1 (KCNK2) and TREK-2 (KCNK10) in the normal human ovary and epithelial ovarian cancer , 2013, Clinical and Translational Oncology.
[37] P. Jonsson,et al. The two-pore domain potassium channel KCNK5: induction by estrogen receptor alpha and role in proliferation of breast cancer cells. , 2011, Molecular endocrinology.
[38] W. Park,et al. Altered expression of KCNK9 in colorectal cancers , 2004, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.