A review on cyclin-dependent kinase 5: An emerging drug target for neurodegenerative diseases
Abstract Cyclin-dependent kinase 5 (CDK5) is the serine/threonine-directed kinase mainly
found in the brain and plays a significant role in developing the central nervous system …
found in the brain and plays a significant role in developing the central nervous system …
CDK5: an oncogene or an anti-oncogene: location location location
Recent studies have uncovered various physiological functions of CDK5 in many
nonneuronal tissues. Upregulation of CDK5 and/or its activator p35 in neurons promotes …
nonneuronal tissues. Upregulation of CDK5 and/or its activator p35 in neurons promotes …
Rational drug combination design in patient-derived avatars reveals effective inhibition of hepatocellular carcinoma with proteasome and CDK inhibitors
Background Hepatocellular carcinoma (HCC) remains difficult to treat due to limited effective
treatment options. While the proteasome inhibitor bortezomib has shown promising …
treatment options. While the proteasome inhibitor bortezomib has shown promising …
Discovery and optimization of highly selective inhibitors of CDK5
MH Daniels, G Malojcic, SL Clugston… - Journal of Medicinal …, 2022 - ACS Publications
Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent monogenic
human disease, but to date, only one therapy (tolvaptan) is approved to treat kidney cysts in …
human disease, but to date, only one therapy (tolvaptan) is approved to treat kidney cysts in …
The value of serum microRNA expression signature in predicting refractoriness to bortezomib-based therapy in multiple myeloma patients
P Robak, I Dróżdż, D Jarych, D Mikulski, E Węgłowska… - Cancers, 2020 - mdpi.com
Simple Summary The proteasome inhibitor bortezomib is currently commonly used for the
treatment of multiple myeloma (MM). MicroRNAs (miRNAs) are small non-coding RNAs that …
treatment of multiple myeloma (MM). MicroRNAs (miRNAs) are small non-coding RNAs that …
CDK9 inhibitors in multiple myeloma: a review of progress and perspectives
J Borowczak, K Szczerbowski, N Ahmadi, Ł Szylberg - Medical oncology, 2022 - Springer
Currently, multiple myeloma is not yet considered a curable disease. Despite the recent
advances in therapy, the average patient lifespan is still unsatisfactory. Recently, CDK9 …
advances in therapy, the average patient lifespan is still unsatisfactory. Recently, CDK9 …
The prognostic value of whole-blood PSMB5, CXCR4, POMP, and RPL5 mRNA expression in patients with multiple myeloma treated with bortezomib
P Robak, D Jarych, D Mikulski, I Dróżdż, E Węgłowska… - Cancers, 2021 - mdpi.com
Simple Summary The mRNA expression of nine previously described genes that may affect
resistance to multiple myeloma (MM), viz., ABCB1, CXCR4, MAF, MARCKS, POMP, PSMB5 …
resistance to multiple myeloma (MM), viz., ABCB1, CXCR4, MAF, MARCKS, POMP, PSMB5 …
Cyclin‐dependent kinase 5 (CDK5) inhibitors in Parkinson disease
Abstract Cyclin‐dependent kinase 5 (Cdk5) is a protein expressed in postmitotic neurons in
the central nervous system (CNS). Cdk5 is activated by p35 and p39 which are neuron …
the central nervous system (CNS). Cdk5 is activated by p35 and p39 which are neuron …
CDK5 as a therapeutic tool for the treatment of Alzheimer's Disease: A Review
S Garemilla, R Kumari, R Kumar - European Journal of Pharmacology, 2024 - Elsevier
Alzheimer's disease (AD) remains one of the most challenging and prevalent
neurodegenerative disorders worldwide. Despite extensive research efforts, effective …
neurodegenerative disorders worldwide. Despite extensive research efforts, effective …
Different Strategies to Overcome Resistance to Proteasome Inhibitors—A Summary 20 Years after Their Introduction
P Tyrna, G Procyk, Ł Szeleszczuk… - … Journal of Molecular …, 2024 - search.proquest.com
Abstract Proteasome inhibitors (PIs), bortezomib, carfilzomib, and ixazomib, are the first-line
treatment for multiple myeloma (MM). They inhibit cytosolic protein degradation in cells …
treatment for multiple myeloma (MM). They inhibit cytosolic protein degradation in cells …