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注意:仅列出部分参考文献,下载原文获取全部文献信息。Mitochondrial Function, Metabolic Regulation, and Human Disease Viewed through the Prism of Sirtuin 4 (SIRT4) Functions
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JOURNAL OF PROTEOME RESEARCH (2019)
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FRONTIERS IN PHYSIOLOGY (2019)
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FRONTIERS IN ENDOCRINOLOGY (2019)
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ONCOLOGY LETTERS (2018)
SIRT4 accelerates Ang II-induced pathological cardiac hypertrophy by inhibiting manganese superoxide dismutase activity
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EUROPEAN HEART JOURNAL (2017)
Molecular modeling, dynamics studies and density functional theory approaches to identify potential inhibitors of SIRT4 protein from Homo sapiens : a novel target for the treatment of type 2 diabetes
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JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2017)
SIRT4 inhibits malignancy progression of NSCLCs, through mitochondrial dynamics mediated by the ERK-Drp1 pathway
L. Fu et al.
ONCOGENE (2017)
SIRT4 overexpression protects against diabetic nephropathy by inhibiting podocyte apoptosis
Jian-Xia Shi et al.
EXPERIMENTAL AND THERAPEUTIC MEDICINE (2017)
Crystal structures of the mitochondrial deacylase Sirtuin 4 reveal isoform-specific acyl recognition and regulation features
Martin Pannek et al.
NATURE COMMUNICATIONS (2017)
Decreased SIRT4 protein levels in endometrioid adenocarcinoma tissues are associated with advanced AJCC stage
Xiaoxi Chen et al.
CANCER BIOMARKERS (2017)
SIRT4 Is a Lysine Deacylase that Controls Leucine Metabolism and Insulin Secretion
Kristin A. Anderson et al.
CELL METABOLISM (2017)
Assessing sirtuin expression in endometrial carcinoma and non-neoplastic endometrium
Carla Bartosch et al.
ONCOTARGET (2016)
SIRT4 regulates cancer cell survival and growth after stress
Seung Min Jeong et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2016)
Mitochondrial Sirtuins in Cancer: Emerging Roles and Therapeutic Potential
Jasmine George et al.
CANCER RESEARCH (2016)
Using mitochondrial sirtuins as drug targets: disease implications and available compounds
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CELLULAR AND MOLECULAR LIFE SCIENCES (2016)
Mitochondrial sirtuins in the heart
Heiko Bugger et al.
HEART FAILURE REVIEWS (2016)
Acetylation of Mitochondrial Trifunctional Protein α-Subunit Enhances Its Stability To Promote Fatty Acid Oxidation and Is Decreased in Nonalcoholic Fatty Liver Disease
Liang Guo et al.
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Downregulation of SIRT4 Expression Is Associated with Poor Prognosis in Esophageal Squamous Cell Carcinoma
Yujiro Nakahara et al.
ONCOLOGY (2016)
Decreased sirtuin 4 expression is associated with poor prognosis in patients with invasive breast cancer
Qingyu Shi et al.
ONCOLOGY LETTERS (2016)
Sirtuin-4 (SIRT4) is downregulated and associated with some clinicopathological features in gastric adenocarcinoma
Guoyu Huang et al.
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Tumour-suppressive function of SIRT4 in human colorectal cancer
M. Miyo et al.
BRITISH JOURNAL OF CANCER (2015)
Sirtuins in Cancer: a Balancing Act between Genome Stability and Metabolism
Seung Min Jeong et al.
MOLECULES AND CELLS (2015)
CtBP maintains cancer cell growth and metabolic homeostasis via regulating SIRT4
L. Wang et al.
CELL DEATH & DISEASE (2015)
Sirtuin 4 Is a Lipoamidase Regulating Pyruvate Dehydrogenase Complex Activity
Rommel A. Mathias et al.
CELL (2014)
SIRT4 Protein Suppresses Tumor Formation in Genetic Models of Myc-induced B Cell Lymphoma
Seung Min Jeong et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Sorting out functions of sirtuins in cancer
M. Roth et al.
ONCOGENE (2014)
SIRT3 and SIRT4 are mitochondrial tumor suppressor proteins that connect mitochondrial metabolism and carcinogenesis
Yueming Zhu et al.
CANCER & METABOLISM (2014)
SIRT4 regulates ATP homeostasis and mediates a retrograde signaling via AMPK
Linh Ho et al.
AGING-US (2013)
SIRT4 Has Tumor-Suppressive Activity and Regulates the Cellular Metabolic Response to DNA Damage by Inhibiting Mitochondrial Glutamine Metabolism
Seung Min Jeong et al.
CANCER CELL (2013)
The mTORC1 Pathway Stimulates Glutamine Metabolism and Cell Proliferation by Repressing SIRT4
Alfred Csibi et al.
CELL (2013)
Therapeutic strategies impacting cancer cell glutamine metabolism
Michael J. Lukey et al.
FUTURE MEDICINAL CHEMISTRY (2013)
SIRT4 Represses Peroxisome Proliferator-Activated Receptor α Activity To Suppress Hepatic Fat Oxidation
Gaelle Laurent et al.
MOLECULAR AND CELLULAR BIOLOGY (2013)
SIRT4 Coordinates the Balance between Lipid Synthesis and Catabolism by Repressing Malonyl CoA Decarboxylase
Gaelle Laurent et al.
MOLECULAR CELL (2013)
An acetylome peptide microarray reveals specificities and deacetylation substrates for all human sirtuin isoforms
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NATURE COMMUNICATIONS (2013)
Molecular basis for the differential use of glucose and glutamine in cell proliferation as revealed by synchronized HeLa cells
Sergio L. Colombo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Abrogation of Hepatic ATP-Citrate Lyase Protects Against Fatty Liver and Ameliorates Hyperglycemia in Leptin Receptor-Deficient Mice
Qiong Wang et al.
HEPATOLOGY (2009)
c-Myc suppression of miR-23a/b enhances mitochondrial glutaminase expression and glutamine metabolism
Ping Gao et al.
NATURE (2009)
The biology of cancer: Metabolic reprogramming fuels cell growth and proliferation
Ralph J. DeBerardinis et al.
CELL METABOLISM (2008)
Regulation of insulin secretion by SIRT4, a mitochondrial ADP-ribosyltransferase
Nidhi Ahuja et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
A genomic analysis of adult T-cell leukemia
Y. L. Choi et al.
ONCOGENE (2007)
SIRT4 inhibits glutamate dehydrogehase and opposes the effects of calorie restriction in pancreatic β cells
Marcia C. Haigis et al.
CELL (2006)
Histone deacetylases in acute myeloid leukaemia show a distinctive pattern of expression that changes selectively in response to deacetylase inhibitors
C Bradbury et al.
LEUKEMIA (2005)
The human Sir2 ortholog, SIRT2, is an NAD+-dependent tubulin deacetylase
BJ North et al.
MOLECULAR CELL (2003)
The remarkable structural and functional organization of the eukaryotic pyruvate dehydrogenase complexes
ZH Zhou et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Diversity of gene expression in adenocarcinoma of the lung
ME Garber et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)