Evidence map›Paper›PMID 26235622›Full record

ArticleCell reports2015

Serine 62-Phosphorylated MYC Associates with Nuclear Lamins and Its Regulation by CIP2A Is Essential for Regenerative Proliferation.

Kevin Myant, Xi Qiao, Tuuli Halonen, Christophe Come, Anni Laine, Mahnaz Janghorban, Johanna I Partanen, John Cassidy, Erinn-Lee Ogg, Patrizia Cammareri and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Missense Mutations in Myc Box I Influence Nucleocytoplasmic Transport to Promote Leukemogenesis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  4. Article
  5. DNA-PKcs as an upstream mediator of OCT4-induced MYC activation in small cell lung cancer.Biochimica et biophysica acta. Gene regulatory mechanisms · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. CIP2A regulates MYC translation (via its 5'UTR) in colorectal cancer.International journal of colorectal disease · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. MYC protein stability is negatively regulated by BRD4.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  20. 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

16 authors at 6 institutions in 3 countries.

Kevin MyantThe Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Xi QiaoTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland; Department of Pathology, University of Turku, 20520 Turku, Finland.
Tuuli HalonenTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
Christophe ComeTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
Anni LaineTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
Mahnaz JanghorbanDepartment of Molecular and Medical Genetics and Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.
Johanna I PartanenResearch Programs Unit, Translational Cancer Biology and Institute of Biomedicine, University of Helsinki, 00014 Helsinki, Finland.
John CassidyThe Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Erinn-Lee OggThe Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Patrizia CammareriThe Beatson Institute for Cancer Research, Glasgow G61 1BD, UK.
Tiina LaiteräTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
Juha OkkeriTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland.
Juha KlefströmResearch Programs Unit, Translational Cancer Biology and Institute of Biomedicine, University of Helsinki, 00014 Helsinki, Finland.
Rosalie C SearsDepartment of Molecular and Medical Genetics and Knight Cancer Institute, Oregon Health and Science University, Portland, OR 97239, USA.
Owen J SansomThe Beatson Institute for Cancer Research, Glasgow G61 1BD, UK. Electronic address: o.sansom@beatson.gla.ac.uk.
Jukka WestermarckTurku Centre for Biotechnology, University of Turku and Åbo Akademi University, 20520 Turku, Finland; Department of Pathology, University of Turku, 20520 Turku, Finland. Electronic address: jukwes@utu.fi.
Cancer Research UK Scotland Institute · GBÅbo Akademi University · FIOregon Health & Science University · USUniversity of Helsinki · FIUniversity of Turku · FITurku Centre for Biotechnology · FI

Funding

Hydroxylation regulation of c-MycR01CA186241 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mu-Shui Dai, ROSALIE C SEARS · 2015 to 2026
$4.2M
Cellular Mechanisms Controlling Myc Protein StabilityR01CA100855 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SEARS, ROSALIE C · 2003 to 2014
$3.6M
Program in Molecular and Cellular BiosciencesT32GM071338 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI MASLEN, CHERYL L · 2005 to 2020
$3.5M
c-Myc Phosphorylation Sites Regulate Its Apoptotic and Tumorigenic PotentialR01CA129040 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SEARS, ROSALIE C · 2008 to 2012
$1.6M
Cancer Research UK 21139Cancer Research UK A12481NCI NIH HHS R01 CA100855NCI NIH HHS R01 CA129040NCI NIH HHS R01 CA186241NIGMS NIH HHS T32 GM071338Worldwide Cancer Research 08-0614Worldwide Cancer Research 10-0643
6 · The paper itself

Abstract

An understanding of the mechanisms determining MYC's transcriptional and proliferation-promoting activities in vivo could facilitate approaches for MYC targeting. However, post-translational mechanisms that control MYC function in vivo are poorly understood. Here, we demonstrate that MYC phosphorylation at serine 62 enhances MYC accumulation on Lamin A/C-associated nuclear structures and that the protein phosphatase 2A (PP2A) inhibitor protein CIP2A is required for this process. CIP2A is also critical for serum-induced MYC phosphorylation and for MYC-elicited proliferation induction in vitro. Complementary transgenic approaches and an intestinal regeneration model further demonstrated the in vivo importance of CIP2A and serine 62 phosphorylation for MYC activity upon DNA damage. However, targeting of CIP2A did not influence the normal function of intestinal crypt cells. These data underline the importance of nuclear organization in the regulation of MYC phosphorylation, leading to an in vivo demonstration of a strategy for inhibiting MYC activity without detrimental physiological effects.

Indexed as

AnimalsAutoantigensCell NucleusGene Expression Regulation, NeoplasticImmunohistochemistryLamin Type AMembrane ProteinsMiceModels, BiologicalPhosphorylationProto-Oncogene Proteins c-mycAutoantigensKIAA1524 protein, mouseLamin Type AMembrane ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID26235622
PMCPMC4535171
OpenAlexW1560204041

What OpenQuestion holds

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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.