Rushita Adhikari Bagchi
Assistant Professor
Also affiliated: University of Burdwan (2015); St. Boniface Hospital (2012–2018); University of Manitoba (2011–2018); University of Colorado Anschutz (2013–2024); University of Colorado Denver (2013–2021)
Research Areas
Biomedical Subjects
Biography and Research Information
OverviewAI-generated summary
Rushita Adhikari Bagchi's research focuses on the molecular mechanisms underlying cardiovascular and metabolic diseases, particularly investigating the role of histone deacetylases (HDACs) and chromatin remodeling in these conditions.
Her work has explored how dynamic chromatin targeting, specifically involving BRD4, contributes to cardiac fibroblast activation. She has also investigated the therapeutic potential of HDAC inhibition, demonstrating its ability to reverse diastolic dysfunction and modulate extracellular matrix remodeling. Further research has examined the suppression of thermogenic programs in adipose tissue by HDAC11 and the restoration of leptin sensitivity through HDAC6 inhibition in obesity models. Her publications also include studies on oxidative stress and altered energy production in the heart following ischemic acute kidney injury in mice, and the regulation of cardiac fibroblast phenotype by the transcription factor scleraxis.
Bagchi holds a high-impact researcher designation and has an h-index of 26 with 99 total publications and 1,822 total citations. She leads a research group and collaborates with several colleagues at the University of Arkansas for Medical Sciences, including S Ibrahim, Ryan Holdiness, Ashim K. Bagchi, and Se‐Ran Jun.
Metrics
- h-index: 26
- Publications: 98
- Citations: 1,826
Positions
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Assistant Professor 2024–presentUniversity of Arkansas for Medical Sciences Physiology and Cell Biology Institutional directory
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Postdoctoral Fellow 2015–2022University of Colorado - Anschutz Medical Campus Medicine-Cardiology ORCID
Selected Publications
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Cardiac Fibroblasts in Extracellular Matrix Homeostasis and Remodeling (2026)
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Uncovering a novel cell death-independent mechanism of acute anthracycline toxicity in human cardiac fibroblasts (2026)
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Sex-Specific Adipose Transcriptomic Reprogramming Drives Early Inter-Organ Remodeling in Heart and Liver Under Nutrient Excess (2026)
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Hidden Receptor Crosstalk Governs Lymphatic Failure After Cancer Therapy (2026)
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A call to redefine cardiovascular immunobiology around leukocyte plasticity (2026)
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A Defined and Cost-Efficient Strategy for Generating Functionally Quiescent Human iPSC-Derived Cardiac Fibroblasts (2026)
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3-D biomechanics and epigenomics reveal atypical fibroblast responses in cardiometabolic disease (2025)
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Temporal Dynamics of Extracellular Matrix Remodeling in Anthracycline-Induced Cardiotoxicity (2025)
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Interplay between stress, chloride homeostasis, and cardiovascular regulation (2025)
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Simulating Cardiometabolic Disease in a 3D-Microenvironment: Human Cardiac Fibroblast Response to Nutritional Stress (2025)
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Global Transcriptional Profiling of Adipose Tissue Uncovers Unique Sex-Dependent Mechanisms in Acute Obesity: Implications for Adipose-Heart Interorgan Crosstalk (2025)
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Obesity, histone acetylation, and insulin resistance (2024)
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List of contributors (2024)
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Histone Deacetylases in Metabolism: the Known and the Unexplored (2024)
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Proteomics Approach to Identify Anthracycline-induced Cardiotoxicity Mechanisms in Human Cardiac Fibroblasts (2024)
Grants & Funding
As listed on this researcher's institutional profile.
- Research Training Award American Physiological Society
- Mapping the interactome of a lysine demyristoylase in the diabetic heart Brunson Endowment Grant for Cardiovascular Diseases Research/UAMS College of Medicine
- Elucidation of the regulatory role of scleraxis in cardiac fibrosis (Funded by: Canadian Institutes of Health Research (CIHR)/Research Manitoba Predoctoral Research Award)
- HDAC11 in Diabetic Cardiomyopathy American Heart Association Career Development Award
- ABI P. Prather NIH T32 FY26 Y3 State of Arkansas
- A Multi-omics Approach to Identify Mechanisms of HDAC11 mediated Lipid Regulation in the Diabetic Heart Sturgis Endowment Grant for Diabetes Research/UAMS College of Medicine
- Epigenetic regulation of cardiac hypertrophy by BET acetyl-lysine binding proteins (Funded by: Canadian Institutes of Health Research (CIHR) Postdoctoral Research Fellowship)
Collaboration Network
Top Collaborators
- Proteomics Approach to Identify Anthracycline-induced Cardiotoxicity Mechanisms in Human Cardiac Fibroblasts
- List of contributors
- Obesity, histone acetylation, and insulin resistance
- Hidden Receptor Crosstalk Governs Lymphatic Failure After Cancer Therapy
- Cardiac Fibroblasts in Extracellular Matrix Homeostasis and Remodeling
- 3-D biomechanics and epigenomics reveal atypical fibroblast responses in cardiometabolic disease
- Proteomics Approach to Identify Anthracycline-induced Cardiotoxicity Mechanisms in Human Cardiac Fibroblasts
- Global Transcriptional Profiling of Adipose Tissue Uncovers Unique Sex-Dependent Mechanisms in Acute Obesity: Implications for Adipose-Heart Interorgan Crosstalk
- Simulating Cardiometabolic Disease in a 3D-Microenvironment: Human Cardiac Fibroblast Response to Nutritional Stress
- Sex-Specific Adipose Transcriptomic Reprogramming Drives Early Inter-Organ Remodeling in Heart and Liver Under Nutrient Excess
- 3-D biomechanics and epigenomics reveal atypical fibroblast responses in cardiometabolic disease
- Simulating Cardiometabolic Disease in a 3D-Microenvironment: Human Cardiac Fibroblast Response to Nutritional Stress
- Sex-Specific Adipose Transcriptomic Reprogramming Drives Early Inter-Organ Remodeling in Heart and Liver Under Nutrient Excess
- Uncovering a novel cell death-independent mechanism of acute anthracycline toxicity in human cardiac fibroblasts
- Temporal Dynamics of Extracellular Matrix Remodeling in Anthracycline-Induced Cardiotoxicity
- 3-D biomechanics and epigenomics reveal atypical fibroblast responses in cardiometabolic disease
- Interplay between stress, chloride homeostasis, and cardiovascular regulation
- Cardiac Fibroblasts in Extracellular Matrix Homeostasis and Remodeling
- Proteomics Approach to Identify Anthracycline-induced Cardiotoxicity Mechanisms in Human Cardiac Fibroblasts
- List of contributors
- Obesity, histone acetylation, and insulin resistance
- 3-D biomechanics and epigenomics reveal atypical fibroblast responses in cardiometabolic disease
- Global Transcriptional Profiling of Adipose Tissue Uncovers Unique Sex-Dependent Mechanisms in Acute Obesity: Implications for Adipose-Heart Interorgan Crosstalk
- Simulating Cardiometabolic Disease in a 3D-Microenvironment: Human Cardiac Fibroblast Response to Nutritional Stress
- Sex-Specific Adipose Transcriptomic Reprogramming Drives Early Inter-Organ Remodeling in Heart and Liver Under Nutrient Excess
- Uncovering a novel cell death-independent mechanism of acute anthracycline toxicity in human cardiac fibroblasts
- Uncovering a novel cell death-independent mechanism of acute anthracycline toxicity in human cardiac fibroblasts
- Cardiac Fibroblasts in Extracellular Matrix Homeostasis and Remodeling
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
- Scleraxis and fibrosis in the pressure-overloaded heart
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