User profiles for M. Teresa Borrello
Maria Teresa BorrelloUniversity of Sunderland Verified email at sunderland.ac.uk Cited by 361 |
Protein recognition by short peptide reversible inhibitors of the chromatin-modifying LSD1/CoREST lysine demethylase
M Tortorici, MT Borrello, M Tardugno… - ACS chemical …, 2013 - ACS Publications
The combinatorial assembly of protein complexes is at the heart of chromatin biology. Lysine
demethylase LSD1(KDM1A)/CoREST beautifully exemplifies this concept. The active site of …
demethylase LSD1(KDM1A)/CoREST beautifully exemplifies this concept. The active site of …
Evidencing a pancreatic ductal adenocarcinoma subpopulation sensitive to the proteasome inhibitor carfilzomib
…, E Telle, P Santofimia-Castano, MT Borrello… - Clinical Cancer …, 2020 - AACR
Purpose: Pancreatic ductal adenocarcinoma (PDAC) is a lethal cancer with a survival rate
less than 5%. Multiple chemotherapeutic drugs have been tested to improve patient prognosis…
less than 5%. Multiple chemotherapeutic drugs have been tested to improve patient prognosis…
Loss of activating transcription factor 3 prevents KRAS-mediated pancreatic cancer
The unfolded protein response (UPR) is activated in pancreatic pathologies and suggested
as a target for therapeutic intervention. In this study, we examined activating transcription …
as a target for therapeutic intervention. In this study, we examined activating transcription …
Efficient synthesis and biological evaluation of proximicins A, B and C
F Brucoli, A Natoli, P Marimuthu, MT Borrello… - Bioorganic & medicinal …, 2012 - Elsevier
A quick and efficient synthesis and the biological evaluation of promising antitumor-antibiotics
proximicins A, B and C are reported. The characteristic repetitive unit of these molecules, …
proximicins A, B and C are reported. The characteristic repetitive unit of these molecules, …
Chronic liver diseases: From development to novel pharmacological therapies: IUPHAR Review 37
MT Borrello, D Mann - British Journal of Pharmacology, 2023 - Wiley Online Library
Chronic liver diseases comprise a broad spectrum of burdensome diseases that still lack
effective pharmacological therapies. Our research group focuses on fibrosis, which is a major …
effective pharmacological therapies. Our research group focuses on fibrosis, which is a major …
The unfolded protein response: An emerging therapeutic target for pancreatitis and pancreatic ductal adenocarcinoma
MT Borrello, MB Martin, CL Pin - Pancreatology, 2022 - Elsevier
Pancreatitis is a debilitating disease involving inflammation and fibrosis of the exocrine
pancreas. Recurrent or chronic forms of pancreatitis are a significant risk factor for pancreatic …
pancreas. Recurrent or chronic forms of pancreatitis are a significant risk factor for pancreatic …
cis‐cyclopropylamines as mechanism‐based inhibitors of monoamine oxidases
T Malcomson, K Yelekci, MT Borrello… - The FEBS …, 2015 - Wiley Online Library
Cyclopropylamines, inhibitors of monoamine oxidases ( MAO ) and lysine‐specific
demethylase ( LSD 1), provide a useful structural scaffold for the design of mechanism‐based …
demethylase ( LSD 1), provide a useful structural scaffold for the design of mechanism‐based …
[HTML][HTML] LSD1 inhibition attenuates androgen receptor V7 splice variant activation in castration resistant prostate cancer models
…, AL Hayden, LR Douglas, PJ Duriez, MT Borrello… - Cancer Cell …, 2018 - Springer
Background Castrate resistant prostate cancer (CRPC) is often driven by constitutively
active forms of the androgen receptor such as the V7 splice variant (AR-V7) and commonly …
active forms of the androgen receptor such as the V7 splice variant (AR-V7) and commonly …
[HTML][HTML] Expanding the druggable space of the LSD1/CoREST epigenetic target: new potential binding regions for drug-like molecules, peptides, protein partners, and …
…, M Tortorici, G Ciossani, MT Borrello… - PLoS computational …, 2013 - journals.plos.org
Lysine specific demethylase-1 (LSD1/KDM1A) in complex with its corepressor protein
CoREST is a promising target for epigenetic drugs. No therapeutic that targets LSD1/CoREST, …
CoREST is a promising target for epigenetic drugs. No therapeutic that targets LSD1/CoREST, …
Fluorinated tranylcypromine analogues as inhibitors of lysine-specific demethylase 1 (LSD1, KDM1A)
MT Borrello, B Schinor, K Bartels, H Benelkebir… - Bioorganic & Medicinal …, 2017 - Elsevier
We report a series of tranylcypromine analogues containing a fluorine in the cyclopropyl ring.
A number of compounds with additional m- or p-substitution of the aryl ring were …
A number of compounds with additional m- or p-substitution of the aryl ring were …