Massimo Donadelli

ORCID: 0000-0001-9224-9230
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Autophagy in Disease and Therapy
  • Cancer, Hypoxia, and Metabolism
  • Cancer-related Molecular Pathways
  • Pancreatic and Hepatic Oncology Research
  • Epigenetics and DNA Methylation
  • Chronic Lymphocytic Leukemia Research
  • Histone Deacetylase Inhibitors Research
  • Mitochondrial Function and Pathology
  • RNA Interference and Gene Delivery
  • MicroRNA in disease regulation
  • Cancer Research and Treatments
  • Peptidase Inhibition and Analysis
  • Pancreatic function and diabetes
  • Adipose Tissue and Metabolism
  • RNA modifications and cancer
  • Cancer Cells and Metastasis
  • Immunotherapy and Immune Responses
  • Lymphoma Diagnosis and Treatment
  • Acute Lymphoblastic Leukemia research
  • Ubiquitin and proteasome pathways
  • Drug Transport and Resistance Mechanisms
  • Advanced Proteomics Techniques and Applications
  • Metabolism, Diabetes, and Cancer
  • PI3K/AKT/mTOR signaling in cancer
  • NF-κB Signaling Pathways

University of Verona
2016-2025

Universidade Federal de Alfenas
2019

Institute for Biomedicine
2017

Zero to Three
2009

Charles University
2007

Instituto de Química Física Blas Cabrera
2006-2007

Czech Academy of Sciences, Institute of Biophysics
2007

Czech Academy of Sciences, Institute of Animal Physiology and Genetics
2007

GlaxoSmithKline (Italy)
2005

European Institute of Oncology
2005

Gemcitabine (GEM, 2′,2′-difluorodeoxycytidine) is currently used in advanced pancreatic adenocarcinoma, with a response rate of < 20%. The purpose our work was to improve GEM activity by addition cannabinoids. Here, we show that induces both cannabinoid receptor-1 (CB1) and receptor-2 (CB2) receptors an NF-κB-dependent mechanism its association cannabinoids synergistically inhibits adenocarcinoma cell growth increases reactive oxygen species (ROS) induced single treatments. antiproliferative...

10.1038/cddis.2011.36 article EN cc-by Cell Death and Disease 2011-04-28

The anti-tumoral effects of cannabinoids have been described in different tumor systems, including pancreatic adenocarcinoma, but their mechanism action remains unclear. We used specific for the CB1 (ACPA) and CB2 (GW) receptors metabolomic analyses to unravel potential pathways mediating cannabinoid-dependent inhibition cancer cell growth. Panc1 cells treated with show elevated AMPK activation induced by a ROS-dependent increase AMP/ATP ratio. ROS promote nuclear translocation GAPDH, which...

10.1038/cddis.2013.151 article EN cc-by Cell Death and Disease 2013-06-13
Coming Soon ...