[HTML][HTML] Heat-shock proteins in leukemia and lymphoma: multitargets for innovative therapeutic approaches

V Cabaud-Gibouin, M Durand, R Quéré, F Girodon… - Cancers, 2023 - mdpi.com
Simple Summary Heat-shock proteins (HSPs) are molecular chaperones overexpressed in
tumor cells and are necessary for their survival. In leukemia and lymphoma, HSPs have …

[HTML][HTML] The current state of Charcot–Marie–Tooth disease treatment

Y Okamoto, H Takashima - Genes, 2023 - mdpi.com
Charcot–Marie–Tooth disease (CMT) and associated neuropathies are the most
predominant genetically transmitted neuromuscular conditions; however, effective …

The role of viruses in cancer development versus cancer therapy: An oncological perspective

H Javid, A Sharbaf Mashhad, S Yazdani… - Cancer …, 2023 - Wiley Online Library
Despite great medical advances, oncological research is still looking for novel therapeutic
approaches due to the limitation of conventional therapeutic agents. Virotherapy is one of …

[HTML][HTML] Antiandrogen-equipped histone deacetylase inhibitors selectively inhibit androgen receptor (AR) and AR-splice variant (AR-SV) in castration-resistant …

B Chandrasekaran, S Tapadar, B Wu, U Saran, A Tyagi… - Cancers, 2023 - mdpi.com
Simple Summary SBI-46, an antiandrogen-equipped histone deacetylase inhibitor, is the
lead compound developed for targeting castration-resistant prostate cancer (CRPC). We …

[HTML][HTML] The epigenetic function of androgen receptor in prostate cancer progression

T Sawada, Y Kanemoto, T Kurokawa… - Frontiers in Cell and …, 2023 - frontiersin.org
Androgen and androgen deprivation (castration) therapies, including androgen receptor
antagonists, are clinically used to treat patients with prostate cancer. However, most …

4-Phenylbutyric acid attenuates amyloid-β proteotoxicity through activation of HSF-1 in an Alzheimer's disease model of the nematode Caenorhabditis elegans

S Baumanns, F Muehlemeyer, LC Miesbauer… - Biochemical and …, 2023 - Elsevier
Alzheimer's disease (AD) is a neurodegenerative disorder and the most common form of
dementia. The pathogenesis is a complex process, in which the proteotoxicity of amyloid-β …

In‐solution structure and oligomerization of human histone deacetylase 6–an integrative approach

S Shukla, J Komarek, Z Novakova… - The FEBS …, 2023 - Wiley Online Library
Human histone deacetylase 6 (HDAC6) is a structurally unique, multidomain protein
implicated in a variety of physiological processes including cytoskeletal remodelling and the …

Hybrid histone deacetylase inhibitor: an effective strategy for cancer therapy

J Wu, J Nie, Y Luan, Y Ding - Current Medicinal Chemistry, 2023 - ingentaconnect.com
Inhibition of histone deacetylases (HDACs) has proven to be an effective strategy for cancer
therapy. To date, five histone deacetylase inhibitors (HDACis) have been approved for …

Flavonoid-Based Derivatives for Modulating Various Targets of Alzheimer's Disease

J Pandey - Natural Product-based Synthetic Drug Molecules in …, 2023 - Springer
Abstract Alzheimer's disease (AD), an advanced multifactorial neurodegenerative disease
mainly accompanied by cognitive impairment, is the most conversant form of dementia …

Study on the role and mechanism of HDAC6 in Cd-induced inflammation and fibrosis in mice liver

F Guo, N Lei, R Huang, Z Huang, P Zhao, X Xu… - Biology Bulletin, 2023 - Springer
The heavy metal cadmium (Cd) is one of the major environmental pollution toxicants, which
is highly toxic to the environment and can cause damages to many organs after entering …