The CDK4/6 inhibitor revolution—a game-changing era for breast cancer treatment

L Morrison, S Loibl, NC Turner - Nature reviews Clinical oncology, 2024 - nature.com
Abstract Cyclin-dependent kinase (CDK) 4/6 inhibition in combination with endocrine
therapy is the standard-of-care treatment for patients with advanced-stage hormone receptor …

Targeting CDK4 and CDK6 in cancer

S Goel, JS Bergholz, JJ Zhao - Nature Reviews Cancer, 2022 - nature.com
Abstract Cyclin-dependent kinase 4 (CDK4) and CDK6 are critical mediators of cellular
transition into S phase and are important for the initiation, growth and survival of many …

MONARCH 2: abemaciclib in combination with fulvestrant in women with HR+/HER2− advanced breast cancer who had progressed while receiving endocrine therapy

GW Sledge Jr, M Toi, P Neven, J Sohn… - Journal of clinical …, 2017 - ascopubs.org
Purpose MONARCH 2 (ClinicalTrials. gov identifier: NCT02107703) compared the efficacy
and safety of abemaciclib, a selective cyclin-dependent kinase 4 and 6 inhibitor, plus …

Loss of the FAT1 tumor suppressor promotes resistance to CDK4/6 inhibitors via the hippo pathway

Z Li, P Razavi, Q Li, W Toy, B Liu, C **, W Hsieh… - Cancer cell, 2018 - cell.com
Summary Cyclin dependent kinase 4/6 (CDK4/6) inhibitors (CDK4/6i) are effective in breast
cancer; however, drug resistance is frequently encountered and poorly understood. We …

Treating cancer with selective CDK4/6 inhibitors

B O'leary, RS Finn, NC Turner - Nature reviews Clinical oncology, 2016 - nature.com
Uncontrolled cellular proliferation, mediated by dysregulation of the cell-cycle machinery
and activation of cyclin-dependent kinases (CDKs) to promote cell-cycle progression, lies at …

Cyclin D1, cancer progression, and opportunities in cancer treatment

S Qie, JA Diehl - Journal of molecular medicine, 2016 - Springer
Mammalian cells encode three D cyclins (D1, D2, and D3) that coordinately function as
allosteric regulators of cyclin-dependent kinase 4 (CDK4) and CDK6 to regulate cell cycle …

Evaluation of the use of therapeutic peptides for cancer treatment

S Marqus, E Pirogova, TJ Piva - Journal of biomedical science, 2017 - Springer
Cancer along with cardiovascular disease are the main causes of death in the industrialised
countries around the World. Conventional cancer treatments are losing their therapeutic …

Targeting CDK4 and CDK6: from discovery to therapy

CJ Sherr, D Beach, GI Shapiro - Cancer discovery, 2016 - aacrjournals.org
Biochemical and genetic characterization of D-type cyclins, their cyclin D–dependent
kinases (CDK4 and CDK6), and the polypeptide CDK4/6 inhibitor p16INK4 over two …

[HTML][HTML] CDK4/6 inhibitor-mediated cell overgrowth triggers osmotic and replication stress to promote senescence

L Crozier, R Foy, R Adib, A Kar, JA Holt, AU Pareri… - Molecular cell, 2023 - cell.com
Abnormal increases in cell size are associated with senescence and cell cycle exit. The
mechanisms by which overgrowth primes cells to withdraw from the cell cycle remain …

CDK4/6 initiates Rb inactivation and CDK2 activity coordinates cell-cycle commitment and G1/S transition

S Kim, A Leong, M Kim, HW Yang - Scientific reports, 2022 - nature.com
External signaling controls cell-cycle entry until cells irreversibly commit to the cell cycle to
ensure faithful DNA replication. This process is tightly regulated by cyclin-dependent …