Evidence map›Paper›PMID 32665693›Full record

ArticleScientific reports2020

High-throughput screening reveals higher synergistic effect of MEK inhibitor combinations in colon cancer spheroids.

Evelina Folkesson, Barbara Niederdorfer, Vu To Nakstad, Liv Thommesen, Geir Klinkenberg, Astrid Lægreid, Åsmund Flobak

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Evelina Folkesson *Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Barbara Niederdorfer *Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Vu To NakstadDepartment of Biotechnology, SINTEF Materials and Chemistry, Trondheim, Norway.
Liv ThommesenDepartment of Biomedical Laboratory Science, Norwegian University of Science and Technology, Trondheim, Norway.
Geir KlinkenbergDepartment of Biotechnology, SINTEF Materials and Chemistry, Trondheim, Norway.
Astrid LægreidDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Åsmund FlobakDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway. asmund.flobak@ntnu.no.
Norwegian University of Science and Technology · NOSINTEF · NOSt Olav's University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug combinations have been proposed to combat drug resistance, but putative treatments are challenged by low bench-to-bed translational efficiency. To explore the effect of cell culture format and readout methods on identification of synergistic drug combinations in vitro, we studied response to 21 clinically relevant drug combinations in standard planar (2D) layouts and physiologically more relevant spheroid (3D) cultures of HCT-116, HT-29 and SW-620 cells. By assessing changes in viability, confluency and spheroid size, we were able to identify readout- and culture format-independent synergies, as well as synergies specific to either culture format or readout method. In particular, we found that spheroids, compared to 2D cultures, were generally both more sensitive and showed greater synergistic response to combinations involving a MEK inhibitor. These results further shed light on the importance of including more complex culture models in order to increase the efficiency of drug discovery pipelines.

Indexed as

Early Detection of CancerAntineoplastic AgentsColonic NeoplasmsHigh-Throughput Screening AssaysHT29 CellsHumansMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsSpheroids, CellularAntineoplastic AgentsMitogen-Activated Protein Kinase KinasesProtein Kinase Inhibitors

Identifiers

PMID32665693
PMCPMC7360566
OpenAlexW3043614762

What Socratic 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 Socratic graph.