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1. Full Text Sphingolipids in Atherosclerosis and Vascular Biology
by Chatterjee, Subroto
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 10/1998, Volume 18, Issue 10, pp. 1523 - 1533
Sphingolipids and their metabolic products are now known to have second-messenger functions in a variety of cellular signaling pathways. Lactosylceramide... 
Cell proliferation | Signal transduction | Lipoproteins | Neutral sphingomyelinase | Apoptosis | FAMILIAL HYPERCHOLESTEROLEMIC HOMOZYGOTES | ACTIVATED PROTEIN-KINASE | cell proliferation | TYROSINE PHOSPHORYLATION | signal transduction | INDUCED APOPTOSIS | LOW-DENSITY-LIPOPROTEIN | apoptosis | PROXIMAL TUBULAR CELLS | SIGNAL-TRANSDUCTION | neutral sphingomyelinase | GROWTH-FACTOR RECEPTOR | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | lipoproteins | SMOOTH-MUSCLE CELLS | C-FOS EXPRESSION
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2. Full Text CB2-receptor stimulation attenuates TNF-α-induced human endothelial cell activation, transendothelial migration of monocytes, and monocyte-endothelial adhesion
by Mohanraj Rajesh and Partha Mukhopadhyay and Sándor Bátkai and György Haskó and Lucas Liaudet and John W. Huffman and Anna Csiszar and Zoltan Ungvari and Ken Mackie and Subroto Chatterjee and Pál Pacher
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 10/2007, Volume 293, Issue 4, pp. 2210 - 2218
Targeting cannabinoid-2 (CB2) receptors with selective agonists may represent a novel therapeutic avenue in various inflammatory diseases, but the mechanisms... 
Adhesion molecules | Inflammation | RhoA | Endothelial activation | C-REACTIVE PROTEIN | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | MOLECULE EXPRESSION | ATHEROSCLEROSIS | NECROSIS-FACTOR-ALPHA | KNOCKOUT MICE | endothelial activation | CANNABINOID RECEPTORS | inflammation | adhesion molecules | NITRIC-OXIDE | THERAPEUTIC TARGETS | PERIPHERAL VASCULAR DISEASE | POTENTIAL ROLE | CB2 RECEPTOR ACTIVATION | Inflammation - chemically induced | Leukocyte Rolling - drug effects | Tumor Necrosis Factor-alpha - metabolism | Receptor, Cannabinoid, CB2 - agonists | Humans | Male | Monocytes - metabolism | NF-kappa B - metabolism | rhoA GTP-Binding Protein - metabolism | Aorta - metabolism | RNA, Messenger - metabolism | Receptor, Cannabinoid, CB2 - genetics | Coronary Vessels - metabolism | Lipopolysaccharides | Dose-Response Relationship, Drug | Inflammation - metabolism | Anti-Inflammatory Agents - therapeutic use | Chemokine CCL2 - metabolism | Disease Models, Animal | Coronary Vessels - drug effects | Anti-Inflammatory Agents - pharmacology | Endothelial Cells - metabolism | Aorta - drug effects | Mice, Inbred C57BL | Cells, Cultured | Cannabinoids - pharmacology | Monocytes - drug effects | Receptor, Cannabinoid, CB1 - metabolism | Receptor, Cannabinoid, CB2 - metabolism | Cannabinoids - therapeutic use | Intercellular Adhesion Molecule-1 - metabolism | Animals | Signal Transduction - drug effects | Inflammation - prevention & control | Mice | Vascular Cell Adhesion Molecule-1 - metabolism | Endothelial Cells - drug effects
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3. Full Text The Glycoproteomics–MS for Studying Glycosylation in Cardiac Hypertrophy and Heart Failure
by Yang, Shuang and Chatterjee, Subroto and Cipollo, John
PROTEOMICS – Clinical Applications, ISSN 1862-8346, 09/2018, Volume 12, Issue 5, pp. e1700075 - n/a
With recent advancements of analytical techniques and mass spectrometric instrumentations, proteomics has been widely exploited to study the regulation of... 
glycoproteomics | glycomics | quaternary amine containing isobaric tag for glycan | mass spectrometry | cardiac hypertrophy | solid‐phase | chemoenzymatic | solid-phase | SIGNALING PATHWAYS | SIALIC-ACID DERIVATIZATION | PROTEIN-KINASE | BIOCHEMICAL RESEARCH METHODS | VON-WILLEBRAND-FACTOR | LEFT-VENTRICULAR HYPERTROPHY | MASS-SPECTROMETRY | INTACT N-GLYCOPEPTIDES | ACUTE MYOCARDIAL-INFARCTION | GENE-EXPRESSION | SMOOTH-MUSCLE-CELLS | Glycoproteins - genetics | Glycomics | Humans | Mass Spectrometry | Protein Processing, Post-Translational - genetics | Polysaccharides - genetics | Cardiomegaly - pathology | Heart Failure - genetics | Glycosylation | Heart Failure - pathology | Proteomics - methods | Cardiomegaly - genetics | Heart failure | Proteins | Heart | Heart enlargement | Analysis | Physiological aspects | Mass spectrometry | Analytical methods | Medical treatment | Glycoproteins | Heart function | Heterogeneity | Spectrometry | Polysaccharides | Stimulants | Failure analysis | Proteomics | Biomarkers | Heart diseases | Hypertrophy
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4. Full Text Inhibition of glycosphingolipid synthesis reverses skin inflammation and hair loss in ApoE−/− mice fed western diet
by Bedja, Djahida and Yan, Wenwen and Lad, Viren and Iocco, Domenica and Sivakumar, Nickash and Bandaru, Veera Venkata Ratnam and Chatterjee, Subroto
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 11463 - 11
Sphingolipids have been accorded numerous biological functions however, the effects of feeding a western diet (diet rich in cholesterol and fat) on skin... 
CELLS | ULCERATIVE DERMATITIS | HUMAN-NEUTROPHILS | PROTEIN | C57BL/6 MICE | MULTIDISCIPLINARY SCIENCES | DISEASE | ATHEROSCLEROSIS | KERATINOCYTES | LACTOSYLCERAMIDE | APOLIPOPROTEIN-E | Hair | Phenotypes | High cholesterol diet | Biodegradability | Dermis | Sphingolipids | Propanol | Cholesterol | High fat diet | Metastases | Apolipoprotein E | Arteriosclerosis | Rodents | Skin
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5. Full Text Inhibition of Glycosphingolipid Synthesis Ameliorates Atherosclerosis and Arterial Stiffness in Apolipoprotein E−/− Mice and Rabbits Fed a High-Fat and -Cholesterol Diet
by Chatterjee, Subroto and Bedja, Djahida and Mishra, Sumita and Amuzie, Christine and Avolio, Alberto and Kass, David A and Berkowitz, Dan and Renehan, Mark
Circulation, ISSN 0009-7322, 06/2014, Volume 129, Issue 23, pp. 2403 - 2413
BACKGROUND—Glycosphingolipids, integral components of the cell membrane, have been shown to serve as messengers, transducing growth factor–initiated... 
Molecular imaging | Mice | Glycosphingolipids | Knockout | Atherosclerosis | atherosclerosis | CARDIAC & CARDIOVASCULAR SYSTEMS | GLUCOSYLCERAMIDE SYNTHASE | SERUM | molecular imaging | GENE KNOCKOUT MICE | mice, knockout | INSULIN SENSITIVITY | ADHESION | METABOLISM | glycosphingolipids | ENDOTHELIAL-CELLS | PERIPHERAL VASCULAR DISEASE | EXPRESSION | DENSITY-LIPOPROTEIN RECEPTOR | Hyperlipidemias - genetics | Calcium - metabolism | Male | Aorta - metabolism | Antigens, CD - metabolism | Dose-Response Relationship, Drug | Pulsatile Flow - drug effects | Cholesterol, Dietary - pharmacology | Diet, High-Fat | Ultrasonography | Lipoproteins, LDL - metabolism | Rabbits | Aorta - diagnostic imaging | Hyperlipidemias - metabolism | Models, Cardiovascular | Aorta - drug effects | Coronary Artery Disease - metabolism | Glycosphingolipids - biosynthesis | Hyperlipidemias - drug therapy | Enzyme Inhibitors - pharmacology | Lactosylceramides - metabolism | Morpholines - pharmacology | Coronary Artery Disease - drug therapy | Mice, Knockout | Gene Expression Regulation - drug effects | Animals | Apolipoproteins E - genetics | Vascular Stiffness - drug effects | Coronary Artery Disease - genetics | Glycosphingolipids - metabolism | Glucosylceramides - metabolism | Animal experimentation | Usage | Physiological aspects | Research | Apolipoproteins | Cholesterol
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6. Full Text Frontispiece: The Glycoproteomics–MS for Studying Glycosylation in Cardiac Hypertrophy and Heart Failure
by Yang, Shuang and Chatterjee, Subroto and Cipollo, John
PROTEOMICS – Clinical Applications, ISSN 1862-8346, 09/2018, Volume 12, Issue 5, pp. 1870042 - n/a
Aberrant protein glycosylation is associated with the occurrence of cardiac hypertrophy. Heart arterial blood contains a biomarker (brain naturetic protein:... 
Heart failure | Heart | Heart enlargement | Proteins | Brain | Polysaccharides | Biomarkers | Glycosylation | Biosynthesis | Cardiovascular diseases | Heart diseases | Coronary artery disease | Glycan | Hypertrophy
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7. Full Text Prevention of cardiac hypertrophy by the use of a glycosphingolipid synthesis inhibitor in ApoE−/− mice
by Mishra, Sumita and Bedja, Djahida and Amuzie, Christine and Avolio, Alberto and Chatterjee, Subroto
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 09/2015, Volume 465, Issue 1, pp. 159 - 164
ApoE−/− mice fed a high fat and high cholesterol (HFHC) diet (20% fat and 1.25% cholesterol) from 12 weeks of age to 36 weeks revealed an age-dependent... 
Cardiac hypertrophy | Lactosylceramide | Glycosphingolipids | Atherosclerotic heart disease | OXIDATIVE STRESS | STRETCH | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERLIPIDEMIA | ATHEROSCLEROSIS | LEFT-VENTRICULAR HYPERTROPHY | BIOPHYSICS | DISEASE | MASS | HYPERTENSION | Apolipoproteins E - deficiency | Natriuretic Peptide, Brain - metabolism | Cardiomegaly - etiology | Diet, High-Fat - adverse effects | Cardiomegaly - pathology | Male | Galactosyltransferases - genetics | Glucosyltransferases - metabolism | Atrial Natriuretic Factor - genetics | Galactosyltransferases - antagonists & inhibitors | Phosphorylation - drug effects | Heart Ventricles - pathology | Glucosyltransferases - genetics | Glucosyltransferases - antagonists & inhibitors | Gene Expression | Natriuretic Peptide, Brain - genetics | Atrial Natriuretic Factor - metabolism | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Cardiotonic Agents - pharmacology | Galactosyltransferases - metabolism | Mice, Knockout | Myocytes, Cardiac - pathology | Animals | Cardiomegaly - prevention & control | Myocytes, Cardiac - drug effects | Mitogen-Activated Protein Kinases - antagonists & inhibitors | Apolipoproteins E - genetics | Glycosphingolipids - antagonists & inhibitors | Glycosphingolipids - metabolism | Myocytes, Cardiac - metabolism | Mitogen-Activated Protein Kinases - genetics | Heart Ventricles - metabolism | Mice | Cardiomegaly - genetics | Cholesterol - adverse effects | Heart Ventricles - drug effects | Mitogen-Activated Protein Kinases - metabolism | Prevention | Heart | Heart enlargement | Diastereomers | Analysis | Apolipoproteins | Gene expression | Gangliosides
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8. Full Text Lactosylceramide synthase β-1,4-GalT-V: A novel target for the diagnosis and therapy of human colorectal cancer
by Chatterjee, Subroto B and Hou, Jennifer and Bandaru, Veera Venkata Ratnam and Pezhouh, Maryam Kherad and Syed Rifat Mannan, Abul Ala and Sharma, Rajni
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 01/2019, Volume 508, Issue 2, pp. 380 - 386
Little is known about an oncogenic signal transducer β-1,4-galactosyltransferase-V (β-1,4-GalT-V), in human colorectal cancer. Using quantitative RT-PCR,... 
UDP-Galactose: β-1,4-galactosyltransferase V | Galactosyltransferase | Biomarker | Lactosylceramide | D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol | Colorectal cancer | GLUCOSYLCERAMIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOSYLATION | SPHINGOLIPID METABOLISM | PDMP | INHIBITION | BIOPHYSICS | BETA-1,4-GALACTOSYLTRANSFERASE V | ROLES | GROWTH | EXPRESSION | UDP-Galactose: beta-1,4-galactosyltransferase V
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9. New vis-tas in Lactosylceramide research
by Chatterjee, Subroto and Mishra, Sumita and Suzuki, Sara Kimiko
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2014, Volume 842, pp. 127 - 138
Humans | Lactosylceramides - metabolism | Biomedical Research - trends | Phospholipases A2 - metabolism | Enzyme Activation - drug effects | Antigens, CD - metabolism | Inflammation - metabolism | Lactosylceramides - pharmacology | Myocytes, Cardiac - drug effects | Models, Biological | Myocytes, Cardiac - metabolism | Antigens, CD - pharmacology | Biomedical Research - methods | Cardiomegaly - metabolism | MEDICINE, RESEARCH & EXPERIMENTAL | PRESSURE-OVERLOAD | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LEFT-VENTRICULAR HYPERTROPHY | CELL BIOLOGY | HEART | WALL STRESS | OBESITY | ERK1/2 | CARDIAC-HYPERTROPHY | GROWTH | BIOLOGY | GENE-EXPRESSION
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10. Full Text Lactosylceramide promotes hypertrophy through ROS generation and activation of ERK1/2 in cardiomyocytes
by Mishra, Sumita and Chatterjee, Subroto
Glycobiology, ISSN 0959-6658, 6/2014, Volume 24, Issue 6, pp. 518 - 531
Hypertrophy is central to several heart diseases; however, not much is known about the role of glycosphingolipids (GSLs) in this phenotype. Since GSLs have... 
Lactosylceramide | Cardiac Hypertrophy | Glycosphingolipids | GLYCOSPHINGOLIPID GLYCOSYLTRANSFERASE | PRESSURE-OVERLOAD | BRAIN NATRIURETIC PEPTIDE | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOSARTAN INTERVENTION | lactosylceramide | LEFT-VENTRICULAR HYPERTROPHY | END-POINT REDUCTION | SIGNALING PATHWAY | REDOX REGULATION | glycosphingolipids | CARDIAC-HYPERTROPHY | cardiac hypertrophy | Cell Line | Cell Survival - drug effects | Reactive Oxygen Species - metabolism | RNA, Messenger - genetics | Lactosylceramides - metabolism | Rats | Cardiomegaly - pathology | Glycosphingolipids - genetics | Antigens, CD - metabolism | Animals | Lactosylceramides - pharmacology | MAP Kinase Signaling System - drug effects | Signal Transduction - drug effects | Cardiomegaly - chemically induced | Glycosphingolipids - metabolism | Myocytes, Cardiac - metabolism | Antigens, CD - pharmacology | Cardiomegaly - metabolism | Original
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11. Full Text Use of a Glycolipid Inhibitor to Ameliorate Renal Cancer in a Mouse Model
by Chatterjee, Subroto and Alsaeedi, Nezar and Hou, Jennifer and Bandaru, Veera Venkata Ratnam and Wu, Lan and Halushka, Marc K and Pili, Roberto and Ndikuyeze, Georges and Haughey, Norman J
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e63726
In a xenograft model wherein, live renal cancer cells were implanted under the kidney capsule in mice, revealed a 30-fold increase in tumor volume over a... 
SPHINGOLIPID METABOLISM | GLYCOSPHINGOLIPID BIOSYNTHESIS | CELLS | ADHESION | ACTIVATED PROTEIN-KINASE | CHOLESTEROL | GLUCOSYLCERAMIDE SYNTHASE | MULTIDISCIPLINARY SCIENCES | RECEPTOR | LACTOSYLCERAMIDE | C-FOS EXPRESSION | Kidney - pathology | Kidney Neoplasms - metabolism | Antigens, CD - metabolism | Enzyme Inhibitors - administration & dosage | Glucosyltransferases - metabolism | Kidney - metabolism | Time Factors | Galactosyltransferases - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - metabolism | Disease Models, Animal | Glucosyltransferases - antagonists & inhibitors | Peptide Fragments - metabolism | Kidney - drug effects | Administration, Oral | Morpholines - administration & dosage | Enzyme Inhibitors - pharmacology | Tumor Suppressor Protein p53 - metabolism | Lactosylceramides - metabolism | Morpholines - pharmacology | Treatment Outcome | Galactosyltransferases - metabolism | Blotting, Western | Disease Progression | Animals | Signal Transduction - drug effects | Tumor Burden - drug effects | Kidney Neoplasms - pathology | Mice | Mice, Inbred BALB C | Kidney Neoplasms - drug therapy | Glucosylceramides - metabolism | Gangliosides | Models | Cancer | TOR protein | Cell proliferation | Pediatrics | Syngeneic grafts | AKT protein | Biosynthesis | Kinases | Ceramide glucosyltransferase | Angiogenesis | Cell growth | Synthesis | Allografts | Rodents | Surgery | Xenografts | Inhibition | Cardiology | Vascular endothelial growth factor | Medical research | AKT1 protein | Kidneys | Rapamycin | Propanol | Gene expression | Inhibitors | Kidney cancer | Kidney diseases | Tumors
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12. Drug eluting stents: Friend or foe? A review of cellular mechanisms behind the effects of paclitaxel and sirolimus eluting stents
by Chatterjee, Subroto and Pandey, Ambarish
Current Drug Metabolism, ISSN 1389-2002, 07/2008, Volume 9, Issue 6, pp. 554 - 566
Coronary artery disease continues to be an important cause of mortality and morbidity. Sirolimus and paclitaxel eluting stents have become an important... 
Sirolimus | Stents | Arterial/aortic smooth muscle cells | Heart disease | Re-endothelialization | Paclitaxel | MAMMALIAN TARGET | paclitaxel | TERM ENDOTHELIAL DYSFUNCTION | stents | BIOCHEMISTRY & MOLECULAR BIOLOGY | NEOINTIMAL HYPERPLASIA | NECROSIS-FACTOR-ALPHA | RANDOMIZED CONTROLLED-TRIAL | DEPENDENT KINASE INHIBITOR | VASCULAR SMOOTH-MUSCLE | re-endothelialization | heart disease | RAT CAROTID-ARTERY | sirolimus | FK506-BINDING PROTEIN FKBP | PHARMACOLOGY & PHARMACY | NF-KAPPA-B | arterial/aortic smooth muscle cells | Sirolimus - therapeutic use | Humans | Graft Occlusion, Vascular - prevention & control | Paclitaxel - adverse effects | Clinical Trials as Topic | Paclitaxel - therapeutic use | Drug-Eluting Stents - adverse effects | Sirolimus - administration & dosage | Antineoplastic Agents, Phytogenic - administration & dosage | Animals | Antineoplastic Agents, Phytogenic - therapeutic use | Paclitaxel - administration & dosage | Graft Occlusion, Vascular - physiopathology | Sirolimus - adverse effects | Antineoplastic Agents, Phytogenic - adverse effects
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13. Full Text Integrated Glycoprotein Immobilization Method for Glycopeptide and Glycan Analysis of Cardiac Hypertrophy
by Yang, Shuang and Mishra, Sumita and Chen, Lijun and Zhou, Jian-ying and Chan, Daniel W and Chatterjee, Subroto and Zhang, Hui
Analytical Chemistry, ISSN 0003-2700, 10/2015, Volume 87, Issue 19, pp. 9671 - 9678
Post-translational modifications of proteins can have a major role in disease initiation and progression. Incredible efforts have recently been made to study... 
CHEMISTRY, ANALYTICAL | PRESSURE-OVERLOAD | MASS-SPECTROMETRIC ANALYSIS | HEART-FAILURE | GENE-EXPRESSION | GLYCOMIC ANALYSIS | TROPONIN-T | N-LINKED GLYCOPROTEINS | SIALIC ACIDS | MYOSIN HEAVY-CHAIN | ALPHA-TROPOMYOSIN | Animals | Energy Metabolism | Male | Mice | Glycoproteins - chemistry | Glycopeptides - analysis | Polysaccharides - analysis | Cardiomegaly - metabolism | Glycopeptides - metabolism | Polysaccharides - metabolism | Usage | Analysis | Enzymatic analysis | Glycoproteins | Sialic acids | Electric properties | Hypertrophy
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14. Full Text Neutral sphingomyelinase: past, present and future
by Chatterjee, Subroto
Chemistry and Physics of Lipids, ISSN 0009-3084, 1999, Volume 102, Issue 1, pp. 79 - 96
Sphingomyelin and its metabolic products are now known to have second messenger functions in a variety of cellular signaling pathways. At the epicenter of the... 
Cell proliferation | Sterol homeostasis | Signal transduction | Atherosclerosis | Apoptosis | atherosclerosis | cell proliferation | signal transduction | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOW-DENSITY-LIPOPROTEIN | STRESS-INDUCED APOPTOSIS | apoptosis | OXIDIZED LDL | FACTOR-ALPHA | SIGNAL-TRANSDUCTION | TUMOR-NECROSIS-FACTOR | BIOPHYSICS | HUMAN ATHEROSCLEROTIC LESIONS | PLASMA-MEMBRANE SPHINGOMYELIN | sterol homeostasis | HL-60 CELL-DIFFERENTIATION | SMOOTH-MUSCLE CELLS | Animals | Sphingomyelin Phosphodiesterase - chemistry | Sphingomyelin Phosphodiesterase - physiology | Forecasting | Humans | Sphingomyelin Phosphodiesterase - metabolism
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