Evidence map›Paper›PMID 29059161›Full record

ArticleOncogene2018

Plk1 phosphorylation of Numb leads to impaired DNA damage response.

C Shao, S-J Chien, E Farah, Z Li, N Ahmad, X Liu

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Combined Inhibition ofInternational journal of molecular sciences · 2023
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  13. [Screening and verification of key genes in T-cell acute lymphoblastic leukemia].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2018
    Article
  14. 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

6 authors at 2 institutions in 1 country.

C ShaoDepartment of Biochemistry, Purdue University, West Lafayette, IN, USA.
S-J ChienDepartment of Comparative Pathobiology, Purdue University, West Lafayette, IN, USA.
E FarahDepartment of Biochemistry, Purdue University, West Lafayette, IN, USA.
Z LiDepartment of Biochemistry, Purdue University, West Lafayette, IN, USA.
N AhmadDepartment of Dermatology, University of Wisconsin, Madison, WI, USA.
X LiuDepartment of Biochemistry, Purdue University, West Lafayette, IN, USA.
Purdue University West Lafayette · USUniversity of Wisconsin–Madison · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Role of Polo-Like Kinase-1 in Melanocytic TransformationR01AR059130 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2010 to 2019
$3.8M
Plk1 in Chemo-resistance of CancerR01CA157429 · NCI · UNIVERSITY OF KENTUCKY · PI XIAOQI LIU · 2011 to 2026
$3.5M
Improving chemotherapy of castration-resistant prostate cancer.R01CA196634 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2016 to 2025
$3.3M
Treatment of Castration-resistant Prostate Cancer (CRPC)R01CA196835 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2016 to 2020
$1.7M
Enhancing anti-neoplastic activity of metformin in prostate cancerR01CA192894 · NCI · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI · 2016 to 2020
$1.7M
Role of SIRT1 in melanocyte biology and melanocyte transformationR01CA176748 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2013 to 2017
$1.6M
BD Fortessa Flow Cytometer for Multi-User Shared FacilityS10OD020029 · OD · PURDUE UNIVERSITY · PI RATLIFF, TIMOTHY L. · 2015 to 2015
$412k
BLRD VA IK6 BX003780NCI NIH HHS P30 CA023168NCI NIH HHS R01 CA157429NCI NIH HHS R01 CA176748NCI NIH HHS R01 CA192894NCI NIH HHS R01 CA196634NCI NIH HHS R01 CA196835NIAMS NIH HHS R01 AR059130NIH HHS S10 OD020029
6 · The paper itself

Abstract

Although Numb is well-recognized as a cell-fate determinant in stem/progenitor cells, accumulating evidence supports that Numb also has a critical role in adult tissues and cancers, in particular, in the context of regulation of tumor suppressor p53. Herein, we identified Numb as a novel substrate of Polo-like kinase 1 (Plk1). Of significance, we showed that Plk1-mediated phosphorylation of Numb leads to its enhanced proteasomal degradation and impaired Numb/p53 pathway, thus providing another mechanism how Plk1 antagonizes p53 during DNA damage response. In addition, the novel phosphorylation event identified by us further supports the notion that post-translational modifications of Numb uncouple Numb from p53 and lead to p53 destabilization. Finally, our data generated from both human cancer cell lines and mouse xenograft model showed that cancer cells carrying the unphosphorylated form of Numb by Plk1 are more sensitive to doxorubicin, a classical chemotherapeutic drug. Therefore, our work may provide future strategies for improving the efficacy of chemotherapy by targeting Numb phosphorylation by Plk1.

Indexed as

DNA DamageAnimalsApoptosisBiomarkers, TumorBone NeoplasmsCell Cycle ProteinsCell ProliferationDoxorubicinFemaleGene Expression Regulation, NeoplasticHumansMembrane ProteinsMiceMice, Inbred NODMice, SCIDNerve Tissue ProteinsBiomarkers, TumorCell Cycle ProteinsDoxorubicinMembrane ProteinsNerve Tissue ProteinsNUMB protein, humanPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID29059161
PMCPMC5931337
OpenAlexW2765909575

What OpenQuestion holds

Textmetadata
LicenceTDM
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.