Chetan P. Hans

ORCID: 0000-0003-1830-9084
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About
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Research Areas
  • Aortic aneurysm repair treatments
  • PARP inhibition in cancer therapy
  • Aortic Disease and Treatment Approaches
  • Asthma and respiratory diseases
  • Coronary Interventions and Diagnostics
  • Macrophage Migration Inhibitory Factor
  • Lipoproteins and Cardiovascular Health
  • Ion Channels and Receptors
  • Immune cells in cancer
  • Cardiac Valve Diseases and Treatments
  • Hormonal Regulation and Hypertension
  • Renin-Angiotensin System Studies
  • IL-33, ST2, and ILC Pathways
  • Infectious Aortic and Vascular Conditions
  • Mangiferin and Mango Extracts
  • NF-κB Signaling Pathways
  • Connective tissue disorders research
  • Antimicrobial Resistance in Staphylococcus
  • Magnesium in Health and Disease
  • Atherosclerosis and Cardiovascular Diseases
  • Protease and Inhibitor Mechanisms
  • Cardiovascular, Neuropeptides, and Oxidative Stress Research
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Muscle Physiology and Disorders
  • Pulmonary Hypertension Research and Treatments

University of Missouri
2017-2023

Nationwide Children's Hospital
2011-2020

Harry S. Truman Memorial Veterans' Hospital
2019

The Ohio State University
2009-2017

Geisinger Medical Center
2012

Louisiana State University Health Sciences Center New Orleans
2006-2010

Mie University
2010

Centre Hospitalier Régional et Universitaire de Nancy
2010

Institute of Pharmacology
2009

Louisiana State University
2007

Journal Article Bayesian lasso regression Get access Chris Hans Department of Statistics, The Ohio State University, Columbus, 43210, U.S.A.hans@stat.osu.edu Search for other works by this author on: Oxford Academic Google Scholar Biometrika, Volume 96, Issue 4, December 2009, Pages 835–845, https://doi.org/10.1093/biomet/asp047 Published: 24 September 2009 history Received: 01 July 2008 Revision received: March

10.1093/biomet/asp047 article EN Biometrika 2009-09-24

Macrophages are essential for skeletal muscle homeostasis, but how their dysregulation contributes to the development of fibrosis in disease remains unclear. Here, we used single-cell transcriptomics determine molecular attributes dystrophic and healthy macrophages. We identified six clusters unexpectedly found that none corresponded traditional definitions M1 or M2 Rather, predominant macrophage signature was characterized by high expression fibrotic factors, galectin-3 (gal-3) osteopontin...

10.1126/sciadv.add9984 article EN cc-by-nc Science Advances 2023-07-07

Several clinical studies have shown the benefits of renin-angiotensin system (RAS) blockade in development diabetes, and a local RAS has been identified pancreatic islets. Angiotensin I-converting enzyme (ACE)2, new component RAS, pancreas, but its role β-cell function remains unknown. Using 8- 16-week-old obese db/db mice, we examined ability ACE2 to alter thereby modulate hyperglycemia.Both nondiabetic lean control (db/m) mice were infected with an adenovirus expressing human...

10.2337/db09-0782 article EN cc-by-nc-nd Diabetes 2010-07-26

Abstract The role of NF-κB in the expression inflammatory genes and its participation overall process chronic diseases acute tissue injury are well established. We others have demonstrated a critical involvement poly(ADP-ribose) polymerase (PARP)-1 during inflammation, part, through relationship with NF-κB. However, mechanism by which PARP-1 affects activation has been elusive. In this study, we show that inhibition gene knockout, knockdown, or pharmacologic blockade prevented p65 nuclear...

10.4049/jimmunol.1000646 article EN The Journal of Immunology 2010-07-08

Aortic valve calcification is the most common form of valvular heart disease, but mechanisms calcific aortic disease (CAVD) are unknown. NOTCH1 mutations associated with malformations and adult-onset in families inherited disease. The Notch signaling pathway critical for multiple cell differentiation processes, its role development CAVD not well understood. aim this study was to investigate molecular changes that occur inhibition valve. members expressed adult cusps, examination diseased...

10.1371/journal.pone.0027743 article EN cc-by PLoS ONE 2011-11-16

MicroRNA miR145 has been implicated in vascular smooth muscle cell differentiation, but its mechanisms of action and downstream targets have not fully defined.

10.1161/circresaha.115.303970 article EN Circulation Research 2014-10-17

Men with castration-resistant prostate cancer (CRPC) face poor prognosis and increased risk of treatment-incurred adverse effects resulting in one the highest mortalities among patient population globally. Immune cells act as double-edged sword depending on tumor microenvironment, which leads to infiltration pro-tumor (M2) macrophages. Development new immunomodulatory therapeutic agents capable targeting hence orchestrating transformation M2 macrophages anti-tumor M1, would substantially...

10.1038/s41598-021-96224-8 article EN cc-by Scientific Reports 2021-08-18

Poly(ADP-ribose) polymerase (PARP) was suggested to play a role in endothelial dysfunction that is associated with number of cardiovascular diseases. We hypothesized PARP may an important atherogenesis and its inhibition attenuate atherosclerotic plaque development experimental model atherosclerosis.Using mouse (apolipoprotein E [ApoE](-/-)) high-fat diet-induced atherosclerosis, we demonstrate association between cell death oxidative stress-associated DNA damage activation within plaques....

10.1161/circulationaha.106.668756 article EN Circulation 2007-04-17

Activation of inflammatory pathways plays a critical role in the development abdominal aortic aneurysms (AAA). Notch1 signaling is significant regulator response; however, its AAA unknown.In an angiotensin II-induced mouse model AAA, activation was observed aneurysmal tissue Apoe(-/-) mice, and similar humans undergoing repair. haploinsufficiency significantly reduced incidence mice response to II. Reconstitution bone marrow-derived cells from Notch1(+/-);Apoe(-/-) (donor) lethally...

10.1161/atvbaha.112.254219 article EN Arteriosclerosis Thrombosis and Vascular Biology 2012-10-20

Background The progression of abdominal aortic aneurysm ( AAA ) involves a sustained influx proinflammatory macrophages, which exacerbate tissue injury by releasing cytokines, chemokines, and matrix metalloproteinases. Previously, we showed that Notch deficiency reduces the development in angiotensin II –induced mouse model preventing infiltration macrophages. Here, examined whether inhibition this prevents small these effects are associated with altered macrophage differentiation. Methods...

10.1161/jaha.114.001064 article EN cc-by-nc-nd Journal of the American Heart Association 2014-10-28

Abstract We recently used a murine model of allergic airway inflammation to show that poly(ADP-ribose) polymerase-1 (PARP-1) plays an important role in the pathogenesis asthma-related lung inflammation. In this study, we PARP-1 inhibition, by novel inhibitor (TIQ-A) or gene deletion, prevented eosinophilic infiltration into airways OVA-challenged mice. Such impairment eosinophil recruitment appeared take place after IgE production. OVA challenge wild-type mice resulted significant increase...

10.4049/jimmunol.177.9.6489 article EN The Journal of Immunology 2006-11-01

Abstract The role of inducible NO synthase (iNOS) in allergic airway inflammation remains elusive. We tested the hypothesis that iNOS plays different roles during acute versus chronic inflammation. Acute and mouse models OVA-induced were used to conduct study. showed deletion was associated with a reduction eosinophilia, mucus hypersecretion, IL-5 IL-13 production upon protocol. Such protection completely abolished Interestingly, pulmonary fibrosis observed wild-type mice under protocol...

10.4049/jimmunol.0904214 article EN The Journal of Immunology 2010-07-29

Aims Infiltration of macrophages and apoptosis vascular smooth muscle cells (VSMCs) promote the development abdominal aortic aneurysm (AAA). Previously, we demonstrated that global Notch1 deficiency prevents formation AAA in a mouse model. Herein, sought to explore cell-specific roles development. Methods results Cell-specific haploinsufficient mice, generated on Apoe-/- background using Cre-lox technology, were infused with angiotensin II (1000 ng/min/kg) for 28 days. haploinsufficiency...

10.1371/journal.pone.0178538 article EN cc-by PLoS ONE 2017-05-31

Objective— Abdominal aortic aneurysm is caused by the accumulation of inflammatory cells in wall. Our recent studies demonstrated that inhibition Notch signaling attenuates abdominal formation shifting macrophage balance towards anti-inflammatory (M2) phenotype. Using IL12p40 −/− (interleukin 12 p40) mice, we investigated effects M2-predominant macrophages on development aneurysm. Approach and Results— Male (8–10 week-old) wild-type mice (n=15) C57BL/6 background were infused with Ang II...

10.1161/atvbaha.118.311969 article EN Arteriosclerosis Thrombosis and Vascular Biology 2019-01-17

Angiotensin-converting enzyme type 2 (ACE2) has been shown to be an important member of the renin angiotensin system. Previously, we observed that central ACE2 reduces development hypertension following chronic II (Ang-II) infusion in syn-hACE2 transgenic (SA) mice, which human transgene is selectively targeted neurons. To study physiological consequences over-expression on cardiac function and hypertrophy, SA non-transgenic (NT) mice were infused with Ang-II (600 ng/kg/min, sc) for 14 days,...

10.1371/journal.pone.0048910 article EN cc-by PLoS ONE 2012-11-14

The aim of this study was to take a combination animal and cell culture approaches examine the individual responses vascular cells varying inflammatory factors in order gain insights on mechanism(s) by which poly(ADP-ribose) polymerase (PARP) inhibition promotes plaque stability. Apolipoprotein (ApoE−/−) mice fed high-fat diet were used as model atherosclerosis. Primary endothelial cells, smooth muscle (SMCs), ex-vivo generated foam (FCs) our vitro studies. PARP significantly decreased...

10.1093/cvr/cvn018 article EN Cardiovascular Research 2008-01-24

We recently showed that poly(ADP-ribose) polymerase (PARP) is activated within atherosclerotic plaques in an animal model of atherosclerosis. Pharmacological inhibition PARP or reduced expression heterozygous animals interferes with atherogenesis and may promote factors plaque stability, possibly reflecting changes inflammatory cellular consistent stability. The current study addresses the hypothesis pharmacological promotes regression. Using a high-fat diet-induced atherosclerosis...

10.1124/jpet.108.145938 article EN Journal of Pharmacology and Experimental Therapeutics 2009-01-05

Abstract Abdominal aortic aneurysm (AAA) is characterized by transmural infiltration of myeloid cells at the vascular injury site. Previously, we reported preventive effects Notch deficiency on development AAA reduction infiltrating cells. In this study, examined if inhibition attenuates progression pre-established and potential implications. Pharmacological inhibitor (N-[N-(3,5-difluorophenacetyl)-L-alanyl]-(S)-phenylglycine t-butyl ester; DAPT) was administered subcutaneously three times a...

10.1038/s41598-019-49682-0 article EN cc-by Scientific Reports 2019-09-17

Naïve macrophages (Mφ) polarize in response to various environmental cues a spectrum of cells that have distinct biological functions. The extreme ends the are classified as M1 and M2 macrophages. Previously, we demonstrated Notch1 deficiency promotes Tgf-β2 dependent M2-polarization mouse model abdominal aortic aneurysm. present studies aimed characterize unique set genes regulated by signaling macrophage polarization. Bone marrow derived isolated from WT or

10.1038/s41598-019-44266-4 article EN cc-by Scientific Reports 2019-05-29
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