Evidence map›Paper›PMID 29464063›Full record

ArticleOncotarget2018

Combined inhibition of CDK and HDAC as a promising therapeutic strategy for both cutaneous and uveal metastatic melanoma.

Renier Heijkants, Karen Willekens, Mark Schoonderwoerd, Amina Teunisse, Maaike Nieveen, Enrico Radaelli, Luuk Hawinkels, Jean-Christophe Marine, Aart Jochemsen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.9field-weighted citation impact, top 4% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 39 citations in OpenAlex.

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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 3 institutions in 2 countries.

Renier HeijkantsDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Karen WillekensLaboratory for Molecular Cancer Biology, VIB Center for Cancer Biology, Leuven, Belgium.
Mark SchoonderwoerdDepartment of Gastroenterology-Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Amina TeunisseDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Maaike NieveenDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Enrico RadaelliMouse Histopathology Core Facility, VIB Center for the Biology of Disease, KU Leuven, Leuven, Belgium.
Luuk HawinkelsDepartment of Gastroenterology-Hepatology, Leiden University Medical Center, Leiden, The Netherlands.
Jean-Christophe MarineLaboratory for Molecular Cancer Biology, VIB Center for Cancer Biology, Leuven, Belgium.
Aart JochemsenDepartment of Molecular Cell Biology, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLKU Leuven · BEVIB-KU Leuven Center for Cancer Biology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Very little to no improvement in overall survival has been seen in patients with advanced non-resectable cutaneous melanoma or metastatic uveal melanoma in decades, highlighting the need for novel therapeutic options. In this study we investigated as a potential novel therapeutic intervention for both cutaneous and uveal melanoma patients a combination of the broad spectrum HDAC inhibitor quisinostat and pan-CDK inhibitor flavopiridol. Both drugs are currently in clinical trials reducing time from bench to bedside. Combining quisinostat and flavopiridol shows a synergistic reduction in cell viability of all melanoma cell lines tested, irrespective of their driver mutations. This synergism was also observed in BRAF

Indexed as

apoptosisCDKHDACmetastasized melanomasynergism

Identifiers

PMID29464063
PMCPMC5814203
OpenAlexW2779961708

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.