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Gene

PML

PML is a gene biomarker in the evidence tier "Cancer actionable (CGI)". This page lists evidence by type: Assay-provider ledger (4), Actionable biomarkers (4), Trial mentions (753), and 6 more evidence types, each linked to its source.

Ensembl ENSG00000140464 UniProt P29590 Matched to Ensembl and UniProt
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Assay-provider ledger Assay-provider ledger 4 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 753 Target-disease associations Target-disease associations 345 Vendor sourcing Vendor sourcing 2,563 Trial-cited literature Trial-cited literature 148 Protein variant mentions Protein variant mentions 2 Literature-extracted relations Literature-extracted relations 37 Assay-provider ledger Assay-provider ledger 4 Actionable biomarkers Actionable biomarkers 4 Trial mentions Trial mentions 753 Target-disease associations Target-disease associations 345 Vendor sourcing Vendor sourcing 2,563 Trial-cited literature Trial-cited literature 148 Protein variant mentions Protein variant mentions 2 Literature-extracted relations Literature-extracted relations 37

Rows recorded per section (log scale)

1 more section with rows · 3 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 PML. 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. Not plotted: 1 dated before 1990 and 6 with no date at all.

Publication mentions: plotted from 1990 to 2023, the years our matched corpus covers.

The yearly numbers
PML 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 69 of 8,738 0.79% not measured
2025 45 of 8,875 0.51% not measured
2024 66 of 8,597 0.77% not measured
2023 45 of 8,275 0.54% 3 of 11,460 0.03%
2022 47 of 8,285 0.57% 12 of 13,598 0.09%
2021 59 of 8,692 0.68% 10 of 15,045 0.07%
2020 46 of 7,640 0.60% 14 of 14,459 0.10%
2019 41 of 7,300 0.56% 10 of 12,159 0.08%
2018 45 of 6,927 0.65% 10 of 11,854 0.08%
2017 44 of 6,558 0.67% 10 of 11,595 0.09%

Assay-provider ledger (4)

Shown in this order: most recent publication first.

Assay-provider ledger
Company Provider class Validation Papers Most recent publication
AB Applied Biosystems Reagent supplier Clinical validation 1 June 17, 2010
BD Transduction Laboratories Reagent supplier Clinical validation 1 June 17, 2010
Santa Cruz Biotechnology Reagent supplier Clinical validation 1 June 17, 2010
Thermo Scientific Reagent supplier Clinical validation 1 June 17, 2010

Actionable biomarkers (4)

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

Actionable biomarkers
Alteration Drug Response Disease Source
PML-RARA fusion All -trans Retinoic Acid (ATRA) response-associated acute myeloid leukemia Cancer Genome Interpreter
PML-RARA fusion Volasertib response-associated acute myeloid leukemia Cancer Genome Interpreter
PML-RARA fusion Arsenic Trioxide response-associated acute myeloid leukemia Cancer Genome Interpreter
PML-RARA fusion All -trans Retinoic Acid (ATRA) response-associated acute promyelocytic leukemia Cancer Genome Interpreter

Trial mentions (753)

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

Trial mentions
Trial Source
NCT00300209 Trial eligibility (AACT)
NCT04657094 Trial eligibility (AACT)
NCT07860775 Trial eligibility (AACT)
NCT01235572 Trial eligibility (AACT)
NCT05672251 Trial eligibility (AACT)

Target-disease associations (345)

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

Target-disease associations
Disease Therapeutic area Source
Acute Leukemia cancer or benign tumor Literature (Europe PMC)
Acute Leukemia cancer or benign tumor Mouse knockout (IMPC)
Adenoid Cystic Breast Carcinoma cancer or benign tumor Cancer Gene Census
Alzheimer disease nervous system disease Literature (Europe PMC)
Ampulla of Vater Carcinoma cancer or benign tumor Cancer Gene Census

Vendor sourcing (2,563)

Shown in this order: alphabetical by organization.

Vendor sourcing
Organization Role Tier Evidence Citation
3B Biotech Research Trial collaborator Named in trial exclusion criteriaTrial eligibility criteria : * Non-relapsing MS Pregnancy or lactation - Contraindication to receive cladribine or to continue anti-CD20 therapies according to local label - Inabilit... View trial NCT06854094
3B Biotech Research Trial collaborator Mentioned in trial textTrial free-text mention PML View trial NCT06854094
AGA Clinical Research Associates, LLC Trial sponsor Named in trial exclusion criteriaTrial eligibility criteria : * Patients who meet any of the following criteria will be excluded from study entry: * Abnormal MARSH score on enrollment histopathology * Elevated celiac... View trial NCT02929316
AGA Clinical Research Associates, LLC Trial sponsor Mentioned in trial textTrial free-text mention PML View trial NCT02929316
ANRS, Emerging Infectious Diseases Trial sponsor Named in trial exclusion criteriaTrial eligibility criteria : * Permanent: * Hepatic cirrhosis * Serious psychiatric illness history * EBV or HHV8 lymphoproliferation (lymphoma, systemic Kaposi's sarcoma or mu... View trial NCT01453192

Trial-cited literature (148)

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

Trial-cited literature
Publication Journal Year Citations
Recent HIV infection and annualized HIV incidence rates among sexual and gender minorities in Brazil and Peru (ImPrEP seroincidence study): a cross-sectional, multicenter study. Lancet regional health. Americas 2023 45
Acute promyelocytic leukaemia: population-based study of epidemiology and outcome with ATRA and oral-ATO from 1991 to 2021. BMC cancer 2023 29
Randomised, placebo-controlled, phase 3 trial of the effect of the omega-3 polyunsaturated fatty acid eicosapentaenoic acid (EPA) on colorectal cancer recurrence and survival after surgery for resectable liver metastases: EPA for Metastasis Trial 2 (EMT2) study protocol. BMJ open 2023 7
Mechanics and functional consequences of nuclear deformations. Nature reviews. Molecular cell biology 2022 358
APASL clinical practice guidance: the diagnosis and management of patients with primary biliary cholangitis. Hepatology international 2022 108

Protein variant mentions (2)

Shown in this order: alphabetical by variant.

Protein variant mentions
Variant Distinct papers Year range Sample papers
p.L217F 1 2020 PMID 32059085
p.L218F 1 2020 PMID 32059085

Literature-extracted relations (37)

Shown in this order: chemicals, then diseases.

Literature-extracted relations
Related entity Kind Source relation label Paper Year
Arsenic Trioxide Chemical associate JAK2V617F myeloproliferative neoplasm eradication by a novel interferon/arsenic therapy involves PML. 2021
Arsenic Trioxide Chemical negative_correlate Molecular remission as a therapeutic objective in acute promyelocytic leukemia. 2018
Tretinoin Chemical negative_correlate Molecular remission as a therapeutic objective in acute promyelocytic leukemia. 2018
Tretinoin Chemical negative_correlate Retinoic acid and arsenic trioxide trigger degradation of mutated NPM1, resulting in apoptosis of AML cells. 2015
Arsenic Trioxide Chemical negative_correlate Arsenic trioxide and all-trans retinoic acid target NPM1 mutant oncoprotein levels and induce apoptosis in NPM1-mutated AML cells. 2015

Organizations publishing (217)

Shown in this order: most papers first.

Organizations publishing
Organization Type Papers Years
Government of the United States of America Government 6 2003 to 2018
Harvard Medical School Academic 6 2012 to 2021
Helmholtz Association of German Research Centres Government 4 2015 to 2021
Mass General Brigham Hospital 4 2012 to 2023
Mayo Clinic Hospital 4 2011 to 2022

Where PML appears

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

312 diseases touched.

Not on this page

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

Browse all biomarker evidence pages