Evidence map›Paper›PMID 33081092›Full record

ArticleInternational journal of molecular sciences2020

Horizontal Combination of MEK and PI3K/mTOR Inhibition in BRAF Mutant Tumor Cells with or without Concomitant PI3K Pathway Mutations.

Dominika Rittler, Eszter Molnár, Marcell Baranyi, Tamás Garay, Luca Hegedűs, Clemens Aigner, József Tóvári, József Tímár, Balázs Hegedűs

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Targeting MAPK in Cancer 2.0.International journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
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.

Dominika Rittler2nd Department of Pathology, Semmelweis University, H-1091 Budapest, Hungary.
Eszter Molnár2nd Department of Pathology, Semmelweis University, H-1091 Budapest, Hungary.
Marcell Baranyi2nd Department of Pathology, Semmelweis University, H-1091 Budapest, Hungary.
Tamás GarayFaculty of Information Technology and Bionics, Pázmány Péter Catholic University, H-1083 Budapest, Hungary.
Luca HegedűsDepartment of Thoracic Surgery, Ruhrlandklinik, University Duisburg-Essen, D-45239 Essen, Germany.
Clemens AignerDepartment of Thoracic Surgery, Ruhrlandklinik, University Duisburg-Essen, D-45239 Essen, Germany.ORCID 0000-0002-7787-991X
József TóváriDepartment of Experimental Pharmacology, National Institute of Oncology, H-1122 Budapest, Hungary.ORCID 0000-0002-5543-3204
József Tímár2nd Department of Pathology, Semmelweis University, H-1091 Budapest, Hungary.
Balázs Hegedűs2nd Department of Pathology, Semmelweis University, H-1091 Budapest, Hungary.ORCID 0000-0002-4341-4153
Semmelweis University · HURuhrlandklinik · DENational Institute of Oncology · HU

Funding

2019 Thematic Excellence Program TUDFO/51757/2019-ITMHungarian National Research, Development and Innovation Office K116151Hungarian National Research, Development and Innovation Office NVKP16-1-2016-0004Hungarian National Research, Development and Innovation Office NVKP-16-1-2016-0020
6 · The paper itself

Abstract

The RAS/RAF and PI3K/Akt pathways play a key regulatory role in cancer and are often hit by oncogenic mutations. Despite molecular targeting, the long-term success of monotherapy is often hampered by de novo or acquired resistance. In the case of concurrent mutations in both pathways, horizontal combination could be a reasonable approach. In our study, we investigated the MEK inhibitor selumetinib and PI3K/mTOR dual inhibitor BEZ235 alone and in combination in BRAF-only mutant and BRAF + PI3K/PTEN double mutant cancer cells using short- and long-term 2D viability assays, spheroid assays, and immunoblots. In the 2D assays, selumetinib was more effective on BRAF-only mutant lines when compared to BRAF + PI3K/PTEN double mutants. Furthermore, combination therapy had an additive effect in most of the lines while synergism was observed in two of the double mutants. Importantly, in the SW1417 BRAF + PI3K double mutant cells, synergism was also confirmed in the spheroid and in the in vivo model. Mechanistically, p-Akt level decreased only in the SW1417 cell line after combination treatment. In conclusion, the presence of concurrent mutations alone did not predict a stronger response to combination treatment. Therefore, additional investigations are warranted to identify predictive factors that can select patients who can benefit from the horizontal combinational inhibition of these two pathways.

Indexed as

Signal TransductionAnimalsAntineoplastic AgentsBenzimidazolesCell Line, TumorDrug Resistance, NeoplasmFemaleHumansImidazolesMAP Kinase Kinase KinasesMelanomaMiceMice, NudeMice, SCIDMutationPhosphatidylinositol 3-KinasesAntineoplastic AgentsAZD 6244BenzimidazolesBRAF protein, humandactolisibImidazolesMAP Kinase Kinase KinasesPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins B-rafPTEN PhosphohydrolaseQuinolinesTOR Serine-Threonine KinasesBEZ235BRAFcombination therapyPI3KPTENselumetinib

Identifiers

PMID33081092
PMCPMC7589607
OpenAlexW3093395270

What OpenQuestion holds

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LicenceCC BY
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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.