Evidence map›Paper›PMID 32375238›Full record

ReviewInternational journal of molecular sciences2020

Targeting ERK-Hippo Interplay in Cancer Therapy.

Karel Vališ, Petr Novák

Open access · goldAbstract readReview
In one paragraph

Review 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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Targeting MAPK in Cancer 2.0.International journal of molecular sciences · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Metabolic landscapes in sarcomas.Journal of hematology & oncology · 2021
    Review
  14. Rapamycin and trametinib: a rational combination for treatment of NSCLC.International journal of biological sciences · 2021
    Article
  15. Review
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

2 authors at 1 institution in 1 country.

Karel VališLaboratory of Structural Biology and Cell Signaling, Institute of Microbiology of the Czech Academy of Sciences, 14220 Prague, Czech Republic.ORCID 0000-0002-3036-4345
Petr NovákLaboratory of Structural Biology and Cell Signaling, Institute of Microbiology of the Czech Academy of Sciences, 14220 Prague, Czech Republic.ORCID 0000-0001-8688-529X
Czech Academy of Sciences · CZ

Funding

Akademie Věd České Republiky RVO61388971Ministerstvo Školství, Mládeže a Tělovýchovy ERA-Net for Research Programmes on Rare Diseases, project ReCognitIONMinisterstvo Školství, Mládeže a Tělovýchovy LQ1604
6 · The paper itself

Abstract

Extracellular signal-regulated kinase (ERK) is a part of the mitogen-activated protein kinase (MAPK) signaling pathway which allows the transduction of various cellular signals to final effectors and regulation of elementary cellular processes. Deregulation of the MAPK signaling occurs under many pathological conditions including neurodegenerative disorders, metabolic syndromes and cancers. Targeted inhibition of individual kinases of the MAPK signaling pathway using synthetic compounds represents a promising way to effective anti-cancer therapy. Cross-talk of the MAPK signaling pathway with other proteins and signaling pathways have a crucial impact on clinical outcomes of targeted therapies and plays important role during development of drug resistance in cancers. We discuss cross-talk of the MAPK/ERK signaling pathway with other signaling pathways, in particular interplay with the Hippo/MST pathway. We demonstrate the mechanism of cell death induction shared between MAPK/ERK and Hippo/MST signaling pathways and discuss the potential of combination targeting of these pathways in the development of more effective anti-cancer therapies.

Indexed as

AnimalsAntineoplastic AgentsExtracellular Signal-Regulated MAP KinasesHippo Signaling PathwayHumansNeoplasmsProtein Kinase InhibitorsProtein Serine-Threonine KinasesSignal TransductionAntineoplastic AgentsExtracellular Signal-Regulated MAP KinasesProtein Kinase InhibitorsProtein Serine-Threonine KinasesapoptosiscancercaspaseERKHippoinhibitorsMAPKMSTnatural compoundsPI3KtherapyYAP

Identifiers

PMID32375238
PMCPMC7247570
OpenAlexW3022556852

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.