[HTML][HTML] Advances in understanding N-glycosylation structure, function, and regulation in health and disease

S Esmail, MF Manolson - European journal of cell biology, 2021 - Elsevier
N-linked glycosylation is a post-translational modification crucial for membrane protein
folding, stability and other cellular functions. Alteration of membrane protein N-glycans is …

Targeting histone deacetylases in diseases: where are we?

R Benedetti, M Conte, L Altucci - Antioxidants & redox signaling, 2015 - liebertpub.com
Significance: Epigenetic inactivation of pivotal genes involved in cell growth is a hallmark of
human pathologies, in particular cancer. Histone acetylation balance obtained through …

BET protein inhibitor JQ1 downregulates chromatin accessibility and suppresses metastasis of gastric cancer via inactivating RUNX2/NID1 signaling

S Zhou, S Zhang, L Wang, S Huang, Y Yuan, J Yang… - Oncogenesis, 2020 - nature.com
Chromatin accessibility is critical for tumor development, whose mechanisms remain
unclear. As a crucial regulator for chromatin remodeling, BRD4 promotes tumor progression …

Transcriptome sequencing reveals that LPS-triggered transcriptional responses in established microglia BV2 cell lines are poorly representative of primary microglia

A Das, SH Kim, S Arifuzzaman, T Yoon, JC Chai… - Journal of …, 2016 - Springer
Background Microglia are resident myeloid cells in the CNS that are activated by infection,
neuronal injury, and inflammation. Established BV2 microglial cell lines have been the …

The Curtius rearrangement: applications in modern drug discovery and medicinal chemistry

AK Ghosh, M Brindisi, A Sarkar - ChemMedChem, 2018 - Wiley Online Library
The Curtius rearrangement is the thermal decomposition of an acyl azide derived from
carboxylic acid to produce an isocyanate as the initial product. The isocyanate can undergo …

Current paradigms in epigenetic anticancer therapeutics and future challenges

M Singh, V Kumar, N Sehrawat, M Yadav… - Seminars in Cancer …, 2022 - Elsevier
Any alteration at the genetic or epigenetic level, may result in multiplex of diseases including
tumorigenesis which ultimately results in the cancer development. Restoration of the normal …

Synergistic effect of JQ 1 and rapamycin for treatment of human osteosarcoma

DH Lee, J Qi, JE Bradner, JW Said… - … journal of cancer, 2015 - Wiley Online Library
Bromodomain and extra terminal domain (BET) proteins are important epigenetic regulators
facilitating the transcription of genes in chromatin areas linked to acetylated histones. JQ1, a …

Discovery of novel and selective SIRT6 inhibitors

MD Parenti, A Grozio, I Bauer, L Galeno… - Journal of medicinal …, 2014 - ACS Publications
SIRT6 is an NAD+-dependent deacetylase with a role in the transcriptional control of
metabolism and aging but also in genome stability and inflammation. Broad therapeutic …

Design, synthesis, and antitumor activity of novel compounds based on 1, 2, 4-triazolophthalazine scaffold: apoptosis-inductive and PCAF-inhibitory effects

A Turky, AH Bayoumi, A Ghiaty, AS El-Azab… - Bioorganic …, 2020 - Elsevier
The antitumor activity of newly synthesised triazolophthalazines (L-45 analogues) 10–32
was evaluated in human hepatocellular carcinoma (HePG-2), breast cancer (MCF-7) …

Quinazolinedione SIRT6 inhibitors sensitize cancer cells to chemotherapeutics

G Sociali, L Galeno, MD Parenti, A Grozio… - European journal of …, 2015 - Elsevier
The NAD+-dependent sirtuin SIRT6 is highly expressed in human breast, prostate, and skin
cancer where it mediates resistance to cytotoxic agents and prevents differentiation. Thus …