Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11247532PMC
http://dx.doi.org/10.18632/oncotarget.28593DOI Listing

Publication Analysis

Top Keywords

correction cyclin
4
cyclin e/cdk2-dependent
4
e/cdk2-dependent phosphorylation
4
phosphorylation mcl-1
4
mcl-1 determines
4
determines stability
4
stability cellular
4
cellular sensitivity
4
sensitivity bh3
4
bh3 mimetics
4

Similar Publications

Head and neck squamous cell carcinomas (HNSCCs) represent a heterogeneous group of tumors with a complex molecular profile. Despite therapeutic advances, patient prognosis remains poor, emphasizing the need for more effective treatment strategies. Traditional chemotherapy, with cisplatin and 5-fluorouracil (5-FU), remains the gold standard but is limited by toxicity and tumor resistance.

View Article and Find Full Text PDF

The generalized many-body expansion for building density matrices (GMBE-DM), truncated at the one-body level and combined with a purification scheme, is applied to rank protein-ligand binding affinities across two cyclin-dependent kinase 2 (CDK2) datasets and one Janus kinase 1 (JAK1) dataset, totaling 28 ligands. This quantum fragmentation-based method achieves strong correlation with experimental binding free energies (R = 0.84), while requiring less than 5 min per complex without extensive parallelization, making it highly efficient for rapid drug screening and lead prioritization.

View Article and Find Full Text PDF

With the rapid introduction of novel breast cancer therapies, recognizing and managing side effects is essential to maintain adherence and improve outcomes. As novel oral endocrine therapies and combination strategies including targeted agents have prolonged progression and in some cases disease-free survival, early recognition and appropriate management of these toxicities is critical to optimize quality of life. Dermatologic adverse events are frequently associated with novel breast cancer therapies including immune checkpoint inhibitors (ICIs), targeted therapies, and antibody-drug conjugates (ADCs).

View Article and Find Full Text PDF

Background: The risk of drug-induced corrected QT interval (QTc) prolongation is an important consideration in clinical decision-making for patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer (mBC). This retrospective analysis described concomitant QTc-prolonging medication use in patients with HR+/HER2- mBC who received first-line (1L) treatment with a cyclin-dependent kinase 4/6 inhibitor (CDK4/6i) plus an aromatase inhibitor (AI).

Methods: This retrospective claims analysis utilized the Optum Clinformatics Data Mart database to identify patients with HR+/HER2- mBC who initiated 1L CDK4/6i plus AI treatment between January 2017 and March 2022.

View Article and Find Full Text PDF