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Gene

CCNE1

CCNE1 is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (25), Actionable biomarkers (1), Trial mentions (31), and 5 more evidence types, each linked to its source.

Ensembl ENSG00000105173 UniProt P24864 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 25 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 31 Target-disease associations Target-disease associations 418 Vendor sourcing Vendor sourcing 82 Trial-cited literature Trial-cited literature 214 Literature-extracted relations Literature-extracted relations 17 Organizations publishing Organizations publishing 287 Assay-provider ledger Assay-provider ledger 25 Actionable biomarkers Actionable biomarkers 1 Trial mentions Trial mentions 31 Target-disease associations Target-disease associations 418 Vendor sourcing Vendor sourcing 82 Trial-cited literature Trial-cited literature 214 Literature-extracted relations Literature-extracted relations 17 Organizations publishing Organizations publishing 287

Rows recorded per section (log scale)

4 sections measured, none recorded

Cancer actionable (CGI)

Curated as clinically actionable in cancer by the Cancer Genome Interpreter.

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The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

Evidence over time

Share of that year: what fraction of the trials and papers our biomarker dictionary matched in a year mention CCNE1. The denominator is documents that mention any gene, not every registered document, so improving the matcher moves both halves and never rewrites history. Gene named in free-text trial records. A mention, not a validated biomarker. Actionable-biomarker and target-disease-association evidence carries no date in our sources, so it is not on this chart. Publication mentions cover only papers cited by a registered clinical trial, not all of PubMed.

Trial mentions: plotted from 1990 to 2026, the years our matched corpus covers.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers. Not plotted: 6 at the structurally incomplete recent edge.

The yearly numbers
CCNE1 per year, by evidence type, the most recent 10 years, newest first; the chart covers 1990 to 2026. The share is of the trials and papers our biomarker dictionary matched that year, not of the literature at large, and a blank year is one our matched corpus does not cover at all.
Year Trial mentions Share of that year Publication mentions Share of that year
2026 2 of 8,738 0.02% not measured
2025 5 of 8,875 0.06% not measured
2024 4 of 8,597 0.05% not measured
2023 4 of 8,275 0.05% 23 of 11,460 0.20%
2022 3 of 8,285 0.04% 18 of 13,598 0.13%
2021 2 of 8,692 0.02% 30 of 15,045 0.20%
2020 2 of 7,640 0.03% 20 of 14,459 0.14%
2019 2 of 7,300 0.03% 23 of 12,159 0.19%
2018 0 of 6,927 0.00% 17 of 11,854 0.14%
2017 1 of 6,558 0.02% 14 of 11,595 0.12%

Assay-provider ledger (25)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
Cell Signaling Technology Reagent supplier Clinical validation 1 August 01, 2021
DakoCytomation Context dependent Clinical validation 1 August 01, 2021
Fitzgerald Industries International Reagent supplier Clinical validation 1 August 01, 2021
Santa Cruz Biotechnology Reagent supplier Clinical validation 2 August 01, 2021
Affymetrix Reagent supplier Clinical validationAnalytical validation 2 November 01, 2020

Actionable biomarkers (1)

Shown in this order: fixed catalogue order, not ranked.

Actionable biomarkers
Alteration Drug Response Disease Source
CCNE1 amplification Cdk2 Inhibitors response-associated No disease recorded Cancer Genome Interpreter

Trial mentions (31)

Shown in this order: fixed catalogue order, not by date.

Trial mentions
Trial Source
NCT07288359 Trial eligibility (AACT)
NCT04469764 Trial eligibility (AACT)
NCT05773820 Trial eligibility (AACT)
NCT05431582 Trial eligibility (AACT)
NCT03718091 Trial eligibility (AACT)

Target-disease associations (418)

Shown in this order: fixed catalogue order, not ranked.

Target-disease associations
Disease Therapeutic area Source
AIDS genetic, familial or congenital disease Literature (Europe PMC)
Abnormality of the skeletal system phenotype GWAS credible sets
Adult-onset autosomal recessive sideroblastic anemia genetic, familial or congenital disease Mouse knockout (IMPC)
Alpha-thalassemia genetic, familial or congenital disease Mouse knockout (IMPC)
Alpha-thalassemia - intellectual disability syndrome linked to chromosome 16 genetic, familial or congenital disease Mouse knockout (IMPC)

Vendor sourcing (82)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
Alliance for Clinical Trials in Oncology Trial sponsor Mentioned in trial textTrial free-text mention CCNE1 View trial NCT02523014
Ambry Genetics (United States) Testing lab / CRO (runs the assay) Clinical-testing interpretation submitted (ClinVar)ClinVar clinical-testing submission The c.1078A>G (p.I360V) alteration is located in exon 11 (coding exon 10) of the CCNE1 gene. This alteration results from a A to G substitution at nucleotide... View ClinVar record SCV003543881.2
Astrazeneca Plc Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria for all Modules: 1. Metastatic MIBC 2. 2nd/3rd line 3. Failed adjuvant/neo-adjuvant chemotherapy \<1 yr 4. 1 lesion ≥10 mm at baseline in the longest diamet... View trial NCT02546661
Astrazeneca Plc Trial sponsor Mentioned in trial textTrial free-text mention CCNE1 View trial NCT02546661
Avenzo Therapeutics, Inc. Trial sponsor Named in trial inclusion criteriaTrial eligibility criteria by study phase and part: i) Phase 1a Monotherapy Dose Escalation: Patients with locally advanced or metastatic HR+/HER2- breast cancer, CCNE1-amplified t... View trial NCT05867251

Trial-cited literature (214)

Shown in this order: newest first, then most cited.

Trial-cited literature
Publication Journal Year Citations
ADAGIO: A Phase IIb, Open-Label, Single-Arm, Multicenter Study Assessing the Efficacy and Safety of Adavosertib (AZD1775) as Treatment for Recurrent or Persistent Uterine Serous Carcinoma. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2025 15
Phase II study of the efficacy and safety of palbociclib in patients with recurrent ovarian cancer. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2025 3
Genomic and transcriptomic analyses of residual invasive triple-negative breast cancer after neoadjuvant chemotherapy in the prospective MIRINAE trial (a randomized phase II trial of adjuvant atezolizumab plus capecitabine compared to capecitabine; KCSG-BR18-21). ESMO open 2025 0
Durable responses to ATR inhibition with ceralasertib in tumors with genomic defects and high inflammation. The Journal of clinical investigation 2024 47
Randomized Phase II Study of Gemcitabine With or Without ATR Inhibitor Berzosertib in Platinum-Resistant Ovarian Cancer: Final Overall Survival and Biomarker Analyses. JCO precision oncology 2024 19

Literature-extracted relations (17)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Epirubicin Chemical positive_correlate EGFR amplification and outcome in a randomised phase III trial of chemotherapy alone or chemotherapy plus panitumumab for advanced gastro-oesophageal cancers. 2021
BORTEZOMIB Chemical associate Synthetic lethality between CCNE1 amplification and loss of BRCA1. 2013
Platinum Chemical associate Synthetic lethality between CCNE1 amplification and loss of BRCA1. 2013
Triple Negative Breast Neoplasms Disease associate Genomic and transcriptomic analyses of residual invasive triple-negative breast cancer after neoadjuvant chemotherapy in the prospective MIRINAE trial (a randomized phase II trial of adjuvant atezolizumab plus capecitabine compared to capecitabine; KCSG-BR18-21). 2025
Neoplasms Disease associate Phase II study of the efficacy and safety of palbociclib in patients with recurrent ovarian cancer. 2025

Organizations publishing (287)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Dana-Farber Cancer Institute Other 21 2011 to 2025
Memorial Sloan Kettering Cancer Center Hospital 19 2010 to 2025
The University of Texas System Academic 15 2009 to 2023
Government of the United States of America Government 12 2014 to 2024
Harvard Medical School Academic 10 2015 to 2024

Where CCNE1 appears

  • animal disease
  • biological_process
  • cancer or benign tumor
  • cardiovascular disease
  • disorder of visual system
  • endocrine system disease
  • gastrointestinal disease
  • genetic, familial or congenital disease
  • hematologic disease
  • immune system disease
  • measurement
  • musculoskeletal or connective tissue disease
  • nervous system disease
  • nutritional or metabolic disease
  • phenotype

375 diseases touched.

Not on this page

Checked, with nothing recorded for this biomarker: fda companion diagnostic assertions, fda biomarker qualification projects, protein variant mentions, and human sample screening reference.

Browse all biomarker evidence pages