Search Results - "Borrello, María Teresa"
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Evidencing a Pancreatic Ductal Adenocarcinoma Subpopulation Sensitive to the Proteasome Inhibitor Carfilzomib
Published in Clinical cancer research (15-10-2020)“…Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer with a survival rate less than 5%. Multiple chemotherapeutic drugs have been tested to improve…”
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2
NUPR1 protects liver from lipotoxic injury by improving the endoplasmic reticulum stress response
Published in The FASEB journal (01-03-2021)“…Non‐alcoholic fatty liver (NAFL) and related syndromes affect one‐third of the adult population in industrialized and developing countries. Lifestyle and…”
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3
Synthesis of Carboxamide‐Containing Tranylcypromine Analogues as LSD1 (KDM1A) Inhibitors Targeting Acute Myeloid Leukemia
Published in ChemMedChem (20-04-2021)“…Lysine‐specific demethylase 1 (LSD1/KDM1A) oxidatively removes methyl groups from histone proteins, and its aberrant activity has been correlated with cancers…”
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4
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy
Published in Plants (Basel) (22-12-2023)“…Susa Valley, located in the Italian Western Alps, has served as a meeting point for cultural, spiritual, and commercial exchange for a long period of history…”
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Expanding the druggable space of the LSD1/CoREST epigenetic target: new potential binding regions for drug-like molecules, peptides, protein partners, and chromatin
Published in PLoS computational biology (01-07-2013)“…Lysine specific demethylase-1 (LSD1/KDM1A) in complex with its corepressor protein CoREST is a promising target for epigenetic drugs. No therapeutic that…”
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6
Chronic liver diseases: From development to novel pharmacological therapies: IUPHAR Review 37
Published in British journal of pharmacology (01-11-2023)“…Chronic liver diseases comprise a broad spectrum of burdensome diseases that still lack effective pharmacological therapies. Our research group focuses on…”
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WED-232 - Discovery of novel small molecule inhibitors of HDAC6 that suppress liver fibrosis
Published in Journal of hepatology (01-06-2023)Get full text
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8
Discovery of novel small molecule inhibitors of HDAC6 that suppress liver fibrosis
Published in Journal of hepatology (01-06-2023)Get full text
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9
NUPR1 interacts with eIF2α and is required for resolution of the ER stress response in pancreatic tissue
Published in The FEBS journal (01-07-2021)“…Nuclear protein 1 (NUPR1) is a stress response protein overexpressed upon cell injury in virtually all organs including the exocrine pancreas. Despite NUPR1's…”
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Loss of activating transcription factor 3 prevents KRAS-mediated pancreatic cancer
Published in Oncogene (29-04-2021)“…The unfolded protein response (UPR) is activated in pancreatic pathologies and suggested as a target for therapeutic intervention. In this study, we examined…”
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cis‐cyclopropylamines as mechanism‐based inhibitors of monoamine oxidases
Published in The FEBS journal (01-08-2015)“…Cyclopropylamines, inhibitors of monoamine oxidases (MAO) and lysine‐specific demethylase (LSD1), provide a useful structural scaffold for the design of…”
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12
Fluorinated tranylcypromine analogues as inhibitors of lysine-specific demethylase 1 (LSD1, KDM1A)
Published in Bioorganic & medicinal chemistry letters (15-05-2017)“…[Display omitted] We report a series of tranylcypromine analogues containing a fluorine in the cyclopropyl ring. A number of compounds with additional m- or…”
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13
Isoform-selective HDAC1/6/8 inhibitors with an imidazo-ketopiperazine cap containing stereochemical diversity
Published in Philosophical transactions of the Royal Society of London. Series B. Biological sciences (05-06-2018)“…A series of hydroxamic acids linked by different lengths to a chiral imidazoketopiperazine scaffold were synthesized. The compounds with linker lengths of 6…”
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14
Isoform-selective HDAC1/6/8 inhibitors with an imidazo-ketopiperazine cap containing stereochemical diversity
Published in Philosophical transactions of the Royal Society of London. Series B. Biological sciences (05-06-2018)“…A series of hydroxamic acids linked by different lengths to a chiral imidazo-ketopiperazine scaffold were synthesized. The compounds with linker lengths of 6…”
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15
Protein Recognition by Short Peptide Reversible Inhibitors of the Chromatin-Modifying LSD1/CoREST Lysine Demethylase
Published in ACS chemical biology (16-08-2013)“…The combinatorial assembly of protein complexes is at the heart of chromatin biology. Lysine demethylase LSD1(KDM1A)/CoREST beautifully exemplifies this…”
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16
Efficient synthesis and biological evaluation of proximicins A, B and C
Published in Bioorganic & medicinal chemistry (15-03-2012)“…A quick and efficient synthesis and the biological evaluation of promising antitumor-antibiotics proximicins A, B and C are reported. The characteristic…”
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Efficient synthesis and biological evaluation of proximicins A, B and C: The Chemistry Biology Interface
Published in Bioorganic & medicinal chemistry (2012)Get full text
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18
Expanding the Druggable Space of the LSD1/CoREST Epigenetic Target: New Potential Binding Regions for Drug-Like Molecules, Peptides, Protein Partners, and Chromatin: e1003158
Published in PLoS computational biology (01-07-2013)“…Lysine specific demethylase-1 (LSD1/KDM1A) in complex with its corepressor protein CoREST is a promising target for epigenetic drugs. No therapeutic that…”
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19
Reversible and irreversible lsd1 inhibitors
Published 01-01-2016“…Environmental factors and lifestyle can alter the way our genes are expressed influencing a network of chemical switches within our cells collectively known as…”
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Dissertation