Pharmacogenomic Analysis Reveals CCNA2 as a Predictive Biomarker of Sensitivity to Polo-Like Kinase I Inhibitor in Gastric Cancer
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Pharmacogenomic Analysis Reveals CCNA2 as a Predictive Biomarker of Sensitivity to Polo-Like Kinase I Inhibitor in Gastric Cancer
Authors
Keywords
-
Journal
Cancers
Volume 12, Issue 6, Pages 1418
Publisher
MDPI AG
Online
2020-06-02
DOI
10.3390/cancers12061418
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- The clinical KRAS(G12C) inhibitor AMG 510 drives anti-tumour immunity
- (2019) Jude Canon et al. NATURE
- BI2536 induces mitotic catastrophe and radiosensitization in human oral cancer cells
- (2018) Chieh-Yuan Cheng et al. Oncotarget
- Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries
- (2018) Freddie Bray et al. CA-A CANCER JOURNAL FOR CLINICIANS
- Ribociclib for HR-Positive, Advanced Breast Cancer
- (2017) NEW ENGLAND JOURNAL OF MEDICINE
- Palbociclib: A Review in HR-Positive, HER2-Negative, Advanced or Metastatic Breast Cancer
- (2017) Esther S. Kim et al. Targeted Oncology
- Targeted therapies for gastric cancer: failures and hopes from clinical trials
- (2017) Maria Apicella et al. Oncotarget
- PLK1 Activation in Late G2 Sets Up Commitment to Mitosis
- (2017) Lilia Gheghiani et al. Cell Reports
- Plk1 Inhibitors in Cancer Therapy: From Laboratory to Clinics
- (2016) Rosie Elizabeth Ann Gutteridge et al. MOLECULAR CANCER THERAPEUTICS
- Suppression of KRas-mutant cancer through the combined inhibition of KRAS with PLK1 and ROCK
- (2016) Jieqiong Wang et al. Nature Communications
- The Bub1–Plk1 kinase complex promotes spindle checkpoint signalling through Cdc20 phosphorylation
- (2016) Luying Jia et al. Nature Communications
- TP53 mutations, expression and interaction networks in human cancers
- (2016) Xiaosheng Wang et al. Oncotarget
- Polo-like kinase 1 inhibitor BI2536 causes mitotic catastrophe following activation of the spindle assembly checkpoint in non-small cell lung cancer cells
- (2015) Minji Choi et al. CANCER LETTERS
- Akt: a new activation mechanism
- (2014) Yuan Gao et al. CELL RESEARCH
- Cell-cycle-regulated activation of Akt kinase by phosphorylation at its carboxyl terminus
- (2014) Pengda Liu et al. NATURE
- Identification of potential synthetic lethal genes to p53 using a computational biology approach
- (2013) Xiaosheng Wang et al. BMC Medical Genomics
- Systematic Identification of Molecular Subtype-Selective Vulnerabilities in Non-Small-Cell Lung Cancer
- (2013) Hyun Seok Kim et al. CELL
- Cancer Genome Landscapes
- (2013) B. Vogelstein et al. SCIENCE
- A randomised phase II trial of the Polo-like kinase inhibitor BI 2536 in chemo-naïve patients with unresectable exocrine adenocarcinoma of the pancreas – a study within the Central European Society Anticancer Drug Research (CESAR) collaborative network
- (2012) K Mross et al. BRITISH JOURNAL OF CANCER
- Phase i study of the Plk1 inhibitor BI 2536 administered intravenously on three consecutive days in advanced solid tumours
- (2012) A. Frost et al. Current Oncology
- Control of cell cycle progression by phosphorylation of cyclin-dependent kinase (CDK) substrates
- (2010) Randy Suryadinata et al. BIOSCIENCE REPORTS
- The Efficacy and Safety of BI 2536, a Novel Plk-1 Inhibitor, in Patients with Stage IIIB/IV Non-small Cell Lung Cancer Who Had Relapsed after, or Failed, Chemotherapy: Results from an Open-Label, Randomized Phase II Clinical Trial
- (2010) Martin Sebastian et al. Journal of Thoracic Oncology
- The Roles of Cyclin A2, B1, and B2 in Early and Late Mitotic Events
- (2010) Delquin Gong et al. MOLECULAR BIOLOGY OF THE CELL
- A Genome-wide RNAi Screen Identifies Multiple Synthetic Lethal Interactions with the Ras Oncogene
- (2009) Ji Luo et al. CELL
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started