The role of epigenetic modifications in drug resistance and treatment of breast cancer
M Karami Fath, A Azargoonjahromi, A Kiani… - Cellular & Molecular …, 2022 - Springer
Background Breast cancer is defined as a biological and molecular heterogeneous disorder
that originates from breast cells. Genetic predisposition is the most important factor giving …
that originates from breast cells. Genetic predisposition is the most important factor giving …
Chalcone derivatives: promising starting points for drug design
Medicinal chemists continue to be fascinated by chalcone derivatives because of their
simple chemistry, ease of hydrogen atom manipulation, straightforward synthesis, and a …
simple chemistry, ease of hydrogen atom manipulation, straightforward synthesis, and a …
Valproic acid and epilepsy: from molecular mechanisms to clinical evidences
M Romoli, P Mazzocchetti, R D'Alonzo… - Current …, 2019 - ingentaconnect.com
After more than a century from its discovery, valproic acid (VPA) still represents one of the
most efficient antiepileptic drugs (AEDs). Pre and post-synaptic effects of VPA depend on a …
most efficient antiepileptic drugs (AEDs). Pre and post-synaptic effects of VPA depend on a …
Hybrid drugs—a strategy for overcoming anticancer drug resistance?
M Szumilak, A Wiktorowska-Owczarek, A Stanczak - Molecules, 2021 - mdpi.com
Despite enormous progress in the treatment of many malignancies, the development of
cancer resistance is still an important reason for cancer chemotherapy failure. Increasing …
cancer resistance is still an important reason for cancer chemotherapy failure. Increasing …
Ketone bodies in neurological diseases: focus on neuroprotection and underlying mechanisms
H Yang, W Shan, F Zhu, J Wu, Q Wang - Frontiers in neurology, 2019 - frontiersin.org
There is growing evidence that ketone bodies, which are derived from fatty acid oxidation
and usually produced in fasting state or on high-fat diets have broad neuroprotective effects …
and usually produced in fasting state or on high-fat diets have broad neuroprotective effects …
Cyclic Peptide Screening Methods for Preclinical Drug Discovery: Miniperspective
X Li, TW Craven, PM Levine - Journal of Medicinal Chemistry, 2022 - ACS Publications
Cyclic peptides are among the most diverse architectures for current drug discovery efforts.
Their size, stability, and ease of synthesis provide attractive scaffolds to engage and …
Their size, stability, and ease of synthesis provide attractive scaffolds to engage and …
Epigenetics of breast cancer: Biology and clinical implication in the era of precision medicine
B Pasculli, R Barbano, P Parrella - Seminars in cancer biology, 2018 - Elsevier
In the last years, mortality from breast cancer has declined in western countries as a
consequence of a more widespread screening resulting in earlier detection, as well as an …
consequence of a more widespread screening resulting in earlier detection, as well as an …
Sodium butyrate ameliorates Deoxynivalenol-induced oxidative stress and inflammation in the porcine liver via NR4A2-mediated histone acetylation
Mycotoxin-induced liver injury is often accompanied by oxidative stress (OS) and
inflammation. This research aimed to explore the potential mechanism of sodium butyrate …
inflammation. This research aimed to explore the potential mechanism of sodium butyrate …
Valproic acid and breast cancer: State of the art in 2021
A Wawruszak, M Halasa, E Okon, W Kukula-Koch… - Cancers, 2021 - mdpi.com
Simple Summary Breast cancer (BC) is the most common cancer diagnosed among women
worldwide. Despite numerous studies, the pathogenesis of BC is still poorly understood, and …
worldwide. Despite numerous studies, the pathogenesis of BC is still poorly understood, and …
Anchor extension: a structure-guided approach to design cyclic peptides targeting enzyme active sites
Despite recent success in computational design of structured cyclic peptides, de novo
design of cyclic peptides that bind to any protein functional site remains difficult. To address …
design of cyclic peptides that bind to any protein functional site remains difficult. To address …