Adrien Grimont

ORCID: 0000-0003-1998-580X
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About
Contact & Profiles
Research Areas
  • Pancreatic and Hepatic Oncology Research
  • Neuroendocrine Tumor Research Advances
  • Neuroblastoma Research and Treatments
  • Cancer, Stress, Anesthesia, and Immune Response
  • Photoreceptor and optogenetics research
  • Mechanisms of cancer metastasis
  • Cancer Genomics and Diagnostics
  • Cancer Cells and Metastasis
  • Estrogen and related hormone effects
  • Pancreatic function and diabetes
  • Epigenetics and DNA Methylation
  • Digestive system and related health
  • Phagocytosis and Immune Regulation
  • Renal and related cancers
  • Pancreatitis Pathology and Treatment
  • Cancer Research and Treatments
  • Immune cells in cancer
  • Renin-Angiotensin System Studies
  • NF-κB Signaling Pathways
  • Click Chemistry and Applications
  • FOXO transcription factor regulation
  • interferon and immune responses
  • Pluripotent Stem Cells Research
  • Hormonal Regulation and Hypertension
  • Reproductive System and Pregnancy

Merus (Netherlands)
2025

Cornell University
2019-2024

Weill Cornell Medicine
2019-2024

Memorial Sloan Kettering Cancer Center
2017

de Duve Institute
2012-2014

Institut Cochin
2010

Inserm
2009-2010

Centre National de la Recherche Scientifique
2008-2009

Sorbonne Université
2008-2009

Université Paris Cité
2008

<h3>Objective</h3> Growing evidence suggests that a phenotypic switch converting pancreatic acinar cells to duct-like can lead intraepithelial neoplasia and eventually invasive ductal adenocarcinoma. Histologically, the onset of this is characterised by co-expression markers in acini, lesion called acinar-to-ductal metaplasia (ADM). The transcriptional regulators required initiate ADM are unknown, but need be identified characterise regulatory networks drive ADM. In study, role transcription...

10.1136/gutjnl-2011-300266 article EN Gut 2012-01-22

The COVID-19 pandemic has caused significant mortality and morbidity around the world. Although effective vaccines have been developed, large parts of world remain unvaccinated while new SARS-CoV-2 strains keep emerging.

10.1128/jvi.01257-21 article EN Journal of Virology 2021-09-15

Abstract Nerves are a notable feature of the tumor microenvironment in some epithelial tumors, but their role malignant progression pancreatic ductal adenocarcinoma (PDAC) is uncertain. Here, we identify dense innervation precancerous lesions, known as intraepithelial neoplasms (PanIN), and describe unique subpopulation neuroendocrine PanIN cells that express neuropeptide substance P (SP) receptor neurokinin 1-R (NK1-R). Using organoid culture, demonstrated sensory neurons promoted...

10.1158/0008-5472.can-16-0899 article EN Cancer Research 2017-01-20

<h3>Objective</h3> The transcription factor SOX9 was recently shown to stimulate ductal gene expression in pancreatic acinar-to-ductal metaplasia and accelerate development of premalignant lesions preceding adenocarcinoma (PDAC). Here, we investigate how operates tumourigenesis. <h3>Design</h3> We analysed genomic transcriptomic data from surgically resected PDAC extended the analysis xenografts samples cell lines. manipulated human lines mouse models developing PDAC. <h3>Results</h3> found...

10.1136/gutjnl-2014-307075 article EN Gut 2014-10-21

Nerves are a notable feature of the tumor microenvironment in some epithelial tumors, but their role malignant progression pancreatic ductal adenocarcinoma (PDAC) is uncertain. Here, we identify dense innervation precancerous lesions, known as intraepithelial neoplasms (PanIN), and describe unique subpopulation neuroendocrine PanIN cells that express neuropeptide substance P (SP) receptor neurokinin 1-R (NK1-R). Using organoid culture, demonstrated sensory neurons promoted proliferation...

10.1158/0008-5472.can-16-0899-t article EN Cancer Research 2017-04-06

Abstract Inflammation in the context of pancreatic injury drives acinar-to-ductal metaplasia (ADM), a cell state that can be hijacked by mutant Kras to drive formation cancer. ADM has been described alternatively bear progenitor features, but extent which lineage reversion is broad feature response and early tumorigenesis - particularlyacross different alleles remains poorly understood. Herein we implement novel Ptf1a-tdTomato mice characterize late progenitors serve as benchmarks define...

10.1158/1538-7445.am2025-6416 article EN Cancer Research 2025-04-21

Renal functions are regulated by steroid sex hormones, but the exhaustive identification of their receptors along nephron is still lacking. Here, we have localized all known nuclear or membrane‐bound hormone and some activators male female mice. Almost present in kidney, them having very restricted localization. Only one gene tested among 11 (ARA54) exhibits a gender difference level its expression. This first “renal map” receptor expression may serve as pre‐requisite for investigating role...

10.1016/j.febslet.2009.04.032 article EN FEBS Letters 2009-05-03

10.1016/j.bbamcr.2008.07.023 article EN publisher-specific-oa Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2008-08-06

SUMMARY Inflammation is essential to the disruption of tissue homeostasis, and, in pancreas, can destabilize identity terminally differentiated acinar cells. Herein we employ lineage-traced mouse models delineate chromatin dynamics that accompany cycle metaplasia and regeneration following pancreatitis, unveil presence an epigenetic memory inflammation pancreatic cell compartment. We observe despite histologic resolution cells fail return their molecular baseline after several months,...

10.1101/2021.11.01.466807 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-11-04

Abstract The transcription factor SOX9 has recently been shown to have a role in the ontogenesis of pancreatic ductal adenocarcinoma (PDAC) through metaplastic changes acinar cells. Nevertheless, mechanisms which operates remain be explored. We analyzed genomic and transcriptomic data from cohort surgically resected cases PDAC (n=90) Australian Pancreatic cancer Genome Initiative (APGI). Genetic aberrations (mutation copy number changes) gene were found 15% patient tumors. Protein expression...

10.1158/1538-7445.am2014-lb-73 article EN Cancer Research 2014-10-01

&lt;div&gt;Abstract&lt;p&gt;Nerves are a notable feature of the tumor microenvironment in some epithelial tumors, but their role malignant progression pancreatic ductal adenocarcinoma (PDAC) is uncertain. Here, we identify dense innervation precancerous lesions, known as intraepithelial neoplasms (PanIN), and describe unique subpopulation neuroendocrine PanIN cells that express neuropeptide substance P (SP) receptor neurokinin 1-R (NK1-R). Using organoid culture, demonstrated sensory neurons...

10.1158/0008-5472.c.6509814 preprint EN 2023-03-31

&lt;div&gt;Abstract&lt;p&gt;Nerves are a notable feature of the tumor microenvironment in some epithelial tumors, but their role malignant progression pancreatic ductal adenocarcinoma (PDAC) is uncertain. Here, we identify dense innervation precancerous lesions, known as intraepithelial neoplasms (PanIN), and describe unique subpopulation neuroendocrine PanIN cells that express neuropeptide substance P (SP) receptor neurokinin 1-R (NK1-R). Using organoid culture, demonstrated sensory neurons...

10.1158/0008-5472.c.6509814.v1 preprint EN 2023-03-31

&lt;p&gt;Figure S1 (Supports Figures 1 and 3) Co-culture of DRG neurons with cell organoid lines. Figure S2 6) Histopathologic techniques for PanIN quantification tumor identification. S3 4) FACS sorting neuroendocrine cells expansion in culture. S4 1) Innervation wild type pancreas PanIN-free acinar tissue axon recruitment by PDAC S5 2) Mouse human PanINs contain NK1-R+ cells. S6 Human duodenal enteroendocrine express the NK1-R. S7 organoids CgA neuronal conditioned media increases...

10.1158/0008-5472.22417341 preprint EN cc-by 2023-03-31

&lt;p&gt;Figure S1 (Supports Figures 1 and 3) Co-culture of DRG neurons with cell organoid lines. Figure S2 6) Histopathologic techniques for PanIN quantification tumor identification. S3 4) FACS sorting neuroendocrine cells expansion in culture. S4 1) Innervation wild type pancreas PanIN-free acinar tissue axon recruitment by PDAC S5 2) Mouse human PanINs contain NK1-R+ cells. S6 Human duodenal enteroendocrine express the NK1-R. S7 organoids CgA neuronal conditioned media increases...

10.1158/0008-5472.22417341.v1 preprint EN cc-by 2023-03-31
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