[HTML][HTML] CDK inhibitors in cancer therapy, an overview of recent development
M Zhang, L Zhang, R Hei, X Li, H Cai… - American journal of …, 2021 - ncbi.nlm.nih.gov
Dysregulated cell division, which leads to aberrant cell proliferation, is one of the key
hallmarks of cancer. Therefore, therapeutic targets that block cell division would be effective …
hallmarks of cancer. Therefore, therapeutic targets that block cell division would be effective …
CDK7 inhibitors as anticancer drugs
GP Sava, H Fan, RC Coombes, L Buluwela… - Cancer and Metastasis …, 2020 - Springer
Abstract Cyclin-dependent kinase 7 (CDK7), along with cyclin H and MAT1, forms the CDK-
activating complex (CAK), which directs progression through the cell cycle via T-loop …
activating complex (CAK), which directs progression through the cell cycle via T-loop …
CDK7 inhibition suppresses super-enhancer-linked oncogenic transcription in MYCN-driven cancer
E Chipumuro, E Marco, CL Christensen, N Kwiatkowski… - Cell, 2014 - cell.com
The MYC oncoproteins are thought to stimulate tumor cell growth and proliferation through
amplification of gene transcription, a mechanism that has thwarted most efforts to inhibit …
amplification of gene transcription, a mechanism that has thwarted most efforts to inhibit …
Targeting cell-cycle machinery in cancer
Abnormal activity of the core cell-cycle machinery is seen in essentially all tumor types and
represents a driving force of tumorigenesis. Recent studies revealed that cell-cycle proteins …
represents a driving force of tumorigenesis. Recent studies revealed that cell-cycle proteins …
RNA cytosine methylation and methyltransferases mediate chromatin organization and 5-azacytidine response and resistance in leukaemia
JX Cheng, L Chen, Y Li, A Cloe, M Yue, J Wei… - Nature …, 2018 - nature.com
The roles of RNA 5-methylcytosine (RNA: m5C) and RNA: m5C methyltransferases (RCMTs)
in lineage-associated chromatin organization and drug response/resistance are unclear …
in lineage-associated chromatin organization and drug response/resistance are unclear …
Genomic modelling of the ESR1 Y537S mutation for evaluating function and new therapeutic approaches for metastatic breast cancer
A Harrod, J Fulton, VTM Nguyen, M Periyasamy… - Oncogene, 2017 - nature.com
Drugs that inhibit estrogen receptor-α (ER) activity have been highly successful in treating
and reducing breast cancer progression in ER-positive disease. However, resistance to …
and reducing breast cancer progression in ER-positive disease. However, resistance to …
Development of a selective CDK7 covalent inhibitor reveals predominant cell-cycle phenotype
CM Olson, Y Liang, A Leggett, WD Park, L Li… - Cell chemical …, 2019 - cell.com
Summary Cyclin-dependent kinase 7 (CDK7) regulates both cell cycle and transcription, but
its precise role remains elusive. We previously described THZ1, a CDK7 inhibitor, which …
its precise role remains elusive. We previously described THZ1, a CDK7 inhibitor, which …
Cyclin-dependent kinase-2 as a target for cancer therapy: progress in the development of CDK2 inhibitors as anti-cancer agents
TA Chohan, H Qian, Y Pan… - Current medicinal …, 2015 - ingentaconnect.com
Cyclin-dependent kinase-2 (CDK2) is a member of protein kinase family. It plays an
important role in regulating various events of eukaryotic cell division cycle. Accumulated …
important role in regulating various events of eukaryotic cell division cycle. Accumulated …
Quantifying CDK inhibitor selectivity in live cells
Concerted multidisciplinary efforts have led to the development of Cyclin-Dependent Kinase
inhibitors (CDKi's) as small molecule drugs and chemical probes of intracellular CDK …
inhibitors (CDKi's) as small molecule drugs and chemical probes of intracellular CDK …
Novel oxindole/benzofuran hybrids as potential dual CDK2/GSK-3β inhibitors targeting breast cancer: design, synthesis, biological evaluation, and in silico studies
The serine/threonine protein kinases CDK2 and GSK-3β are key oncotargets in breast
cancer cell lines, therefore, in the present study three series of oxindole-benzofuran hybrids …
cancer cell lines, therefore, in the present study three series of oxindole-benzofuran hybrids …