Evidence map›Paper›PMID 26812881›Full record

ArticleOncotarget2016

Hydroxyurea synergizes with valproic acid in wild-type p53 acute myeloid leukaemia.

Calum Leitch, Tereza Osdal, Vibeke Andresen, Maren Molland, Silje Kristiansen, Xuan Nhi Nguyen, Øystein Bruserud, Bjørn Tore Gjertsen, Emmet McCormack

Registry-linked trialOpen access · diamondAbstract readComparative Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06199557 (A Phase 1/2 Multicenter Open-label Study to Investigate Treatment of Hydroxyurea in Combination With Valproic Acid), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT06199557 phase1 / phase2recruitingnot on this mapstarted 2024, after this paper: background citation

A Phase 1/2 Multicenter Open-label Study to Investigate Treatment of Hydroxyurea in Combination With Valproic Acid (VPA), or 6- Mercaptopurine in Combination With VPA in Patients With AML or HR-MDS Unfit for Standard Therapy

TypeinterventionalSponsorHaukeland University HospitalRan2024 to 2029Enrolled48ConditionsAcute Myeloid Leukemia, Adult, Myelodysplastic Syndromes, AdultArmsHydroxyurea, Hydroxycarbamide, Valproic acid, 6-Mercaptopurine (6-MP)
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Calum LeitchDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Tereza OsdalDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Vibeke AndresenDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Maren MollandDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Silje KristiansenDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Xuan Nhi NguyenDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Øystein BruserudDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Bjørn Tore GjertsenDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
Emmet McCormackDepartment of Clinical Science, University of Bergen, Bergen, N-5021 Norway.
University of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Palliative care in acute myeloid leukaemia (AML) is inadequate. For elderly patients, unfit for intensive chemotherapy, median survival is 2-3 months. As such, there is urgent demand for low-toxic palliative alternatives. We have repositioned two commonly administered anti-leukaemia drugs, valproic acid (VPA) and hydroxyurea (HU), as a combination therapy in AML. The anti-leukemic effect of VPA and HU was assessed in multiple AML cell lines confirming the superior anti-leukemic effect of combination therapy. Mechanistic studies revealed that VPA amplified the ability of HU to slow S-phase progression and this correlated with significantly increased DNA damage. VPA was also shown to reduce expression of the DNA repair protein, Rad51. Interestingly, the tumour suppressor protein p53 was revealed to mitigate cell cycle recovery following combination induced arrest. The efficacy of combination therapy was validated in vivo. Combination treatment increased survival in OCI-AML3 and patient-derived xenograft mouse models of AML. Therapy response was confirmed by optical imaging with multiplexed near-infrared labelled antibodies. The combination of HU and VPA indicates significant potential in preclinical models of AML. Both compounds are widely available and well tolerated. We believe that repositioning this combination could significantly enhance the palliative care of patients unsuited to intensive chemotherapy.

Indexed as

Drug SynergismAdolescentAdultAgedAged, 80 and overAnimalsAnticonvulsantsAntineoplastic AgentsApoptosisBlotting, WesternCase-Control StudiesCell ProliferationFemaleFluorescent Antibody TechniqueFollow-Up StudiesHumansAnticonvulsantsAntineoplastic AgentsHydroxyureaTP53 protein, humanTumor Suppressor Protein p53Valproic AcidAMLDNA damagehydroxyureap53valproic acid

Identifiers

PMID26812881
PMCPMC4884979
OpenAlexW2259074466

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.