Evidence map›Paper›PMID 36902175›Full record

ReviewInternational journal of molecular sciences2023

When Just One Phosphate Is One Too Many: The Multifaceted Interplay between Myc and Kinases.

Dalila Boi, Elisabetta Rubini, Sara Breccia, Giulia Guarguaglini, Alessandro Paiardini

Open access · goldFull text readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

8 citing papers in PubMed, 14 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

5 authors at 2 institutions in 1 country.

Dalila BoiDepartment of Biochemical Sciences, Sapienza University of Rome, 00185 Rome, Italy.
Elisabetta RubiniDepartment of Biochemical Sciences, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0002-1596-5740
Sara BrecciaDepartment of Biochemical Sciences, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0009-0007-9699-1601
Giulia GuarguagliniInstitute of Molecular Biology and Pathology, National Research Council of Italy, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0002-7541-8183
Alessandro PaiardiniDepartment of Biochemical Sciences, Sapienza University of Rome, 00185 Rome, Italy.ORCID 0000-0001-9078-7545
Sapienza University of Rome · ITInstitute of Molecular Biology and Pathology · IT

Funding

Italian Association for Cancer Research AIRC IG-2021 ID-25648Italian Association for Cancer Research AIRC MFAG-2017 ID-20447
6 · The paper itself

Abstract

Myc transcription factors are key regulators of many cellular processes, with Myc target genes crucially implicated in the management of cell proliferation and stem pluripotency, energy metabolism, protein synthesis, angiogenesis, DNA damage response, and apoptosis. Given the wide involvement of Myc in cellular dynamics, it is not surprising that its overexpression is frequently associated with cancer. Noteworthy, in cancer cells where high Myc levels are maintained, the overexpression of Myc-associated kinases is often observed and required to foster tumour cells' proliferation. A mutual interplay exists between Myc and kinases: the latter, which are Myc transcriptional targets, phosphorylate Myc, allowing its transcriptional activity, highlighting a clear regulatory loop. At the protein level, Myc activity and turnover is also tightly regulated by kinases, with a finely tuned balance between translation and rapid protein degradation. In this perspective, we focus on the cross-regulation of Myc and its associated protein kinases underlying similar and redundant mechanisms of regulation at different levels, from transcriptional to post-translational events. Furthermore, a review of the indirect effects of known kinase inhibitors on Myc provides an opportunity to identify alternative and combined therapeutic approaches for cancer treatment.

Indexed as

Protein Serine-Threonine KinasesProto-Oncogene Proteins c-mycAurora Kinase BCell Line, TumorCell ProliferationPhosphatesAurora Kinase BPhosphatesProtein Serine-Threonine KinasesProto-Oncogene Proteins c-mycAurora-AAurora-BBRD4GSK-3kinase inhibitorskinasesMycPIMPKAPLK1

Identifiers

PMID36902175
PMCPMC10003727
OpenAlexW4322771734

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read6
identifiers read4
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.