Evidence map›Paper›PMID 32023850›Full record

ReviewInternational journal of molecular sciences2020

Beyond Kinase Activity: ERK5 Nucleo-Cytoplasmic Shuttling as a Novel Target for Anticancer Therapy.

Alessandro Tubita, Zoe Lombardi, Ignazia Tusa, Persio Dello Sbarba, Elisabetta Rovida

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 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 15% 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, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Investigation ofIn silico pharmacology · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. OXTRNature communications · 2022
    Article
  14. Article
  15. Targeting MAPK in Cancer 2.0.International journal of molecular sciences · 2022
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. The MEK5/ERK5 Pathway in Health and Disease.International journal of molecular sciences · 2021
    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

5 authors at 1 institution in 1 country.

Alessandro TubitaDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.
Zoe LombardiDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.
Ignazia TusaDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.ORCID 0000-0002-9198-2630
Persio Dello SbarbaDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.ORCID 0000-0001-6411-569X
Elisabetta RovidaDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio", University of Florence, 50134 Florence, Italy.ORCID 0000-0002-5949-3239
University of Florence · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG13466Associazione Italiana per la Ricerca sul Cancro IG15282Associazione Italiana per la Ricerca sul Cancro IG21349
6 · The paper itself

Abstract

The importance of mitogen-activated protein kinases (MAPK) in human pathology is underlined by the relevance of abnormalities of MAPK-related signaling pathways to a number of different diseases, including inflammatory disorders and cancer. One of the key events in MAPK signaling, especially with respect to pro-proliferative effects that are crucial for the onset and progression of cancer, is MAPK nuclear translocation and its role in the regulation of gene expression. The extracellular signal-regulated kinase 5 (ERK5) is the most recently discovered classical MAPK and it is emerging as a possible target for cancer treatment. The bigger size of ERK5 when compared to other MAPK enables multiple levels of regulation of its expression and activity. In particular, the phosphorylation of kinase domain and C-terminus, as well as post-translational modifications and chaperone binding, are involved in ERK5 regulation. Likewise, different mechanisms control ERK5 nucleo-cytoplasmic shuttling, underscoring the key role of ERK5 in the nuclear compartment. In this review, we will focus on the mechanisms involved in ERK5 trafficking between cytoplasm and nucleus, and discuss how these processes might be exploited to design new strategies for cancer treatment.

Indexed as

Antineoplastic AgentsCell NucleusCytoplasmGene Expression Regulation, NeoplasticHumansMAP Kinase Signaling SystemMitogen-Activated Protein Kinase 7Molecular Targeted TherapyNeoplasmsProtein TransportAntineoplastic AgentsMAPK7 protein, humanMitogen-Activated Protein Kinase 7alternative kinase targetingBMK1chaperonesMAPKMAPK7nuclear localizationnuclear signalingprotein phosphorylationSUMOylationubiquitination

Identifiers

PMID32023850
PMCPMC7038028
OpenAlexW3003278171

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.