Evidence map›Paper›PMID 24884503›Full record

ArticleJournal of proteome research2014

Large-scale label-free comparative proteomics analysis of polo-like kinase 1 inhibition via the small-molecule inhibitor BI 6727 (Volasertib) in BRAF(V600E) mutant melanoma cells.

Brian D Cholewa, Molly C Pellitteri-Hahn, Cameron O Scarlett, Nihal Ahmad

Open access · greenAbstract readComparative Study
In one paragraph

Article in Journal of proteome research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

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  14. PLK1, A Potential Target for Cancer Therapy.Translational oncology · 2017
    Review
  15. Article
  16. Review
  17. Proteomic Findings in Melanoma.Journal of proteomics & bioinformatics · 2016
    Article
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Brian D CholewaDepartment of Dermatology, ‡Molecular and Environmental Toxicology Center, and §School of Pharmacy, University of Wisconsin , 1300 University Avenue, Madison, Wisconsin 53706, United States.
Molly C Pellitteri-Hahn
Cameron O Scarlett
Nihal Ahmad
William S. Middleton Memorial Veterans Hospital · US

Funding

Molecular & Environmental Toxicology Pre-& Postdoctoral Training ProgramT32ES007015 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI CHRISTOPHER A BRADFIELD · 1985 to 2026
$11.5M
Role of Polo-Like Kinase-1 in Melanocytic TransformationR01AR059130 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2010 to 2019
$3.8M
Acquisition of a High-Field Dual Source FTICR-MS for Pharmaceutical ResearchS10RR029531 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI LI, LINGJUN · 2011 to 2011
$2.1M
Role of SIRT1 in melanocyte biology and melanocyte transformationR01CA176748 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AHMAD, NIHAL · 2013 to 2017
$1.6M
Plk1-Numb Cooperation in MelanomagenesisI01BX001008 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI AHMAD, NIHAL · 2013 to 2016
–
SHARED GAS CHROMATOGRAPH AND GC/MASS SPECTROMETERS10RR002953 · NCRR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI YOUNG, VERNON R · 1986 to 1986
–
BLRD VA I01 BX001008NCI NIH HHS R01 CA176748NCI NIH HHS R01CA176748NCRR NIH HHS 1S10RR029531−01NCRR NIH HHS S10 RR029531NIAMS NIH HHS R01 AR059130NIAMS NIH HHS R01AR059130NIEHS NIH HHS T32 ES007015NIEHS NIH HHS T32 ES007015-35
6 · The paper itself

Abstract

Polo-like kinase 1 (Plk1) is a serine/threonine kinase that plays a key role during the cell cycle by regulating mitotic entry, progression, and exit. Plk1 is overexpressed in a variety of human cancers and is essential to sustained oncogenic proliferation, thus making Plk1 an attractive therapeutic target. However, the clinical efficacy of Plk1 inhibition has not emulated the preclinical success, stressing an urgent need for a better understanding of Plk1 signaling. This study addresses that need by utilizing a quantitative proteomics strategy to compare the proteome of BRAF(V600E) mutant melanoma cells following treatment with the Plk1-specific inhibitor BI 6727. Employing label-free nano-LC-MS/MS technology on a Q-exactive followed by SIEVE processing, we identified more than 20 proteins of interest, many of which have not been previously associated with Plk1 signaling. Here we report the down-regulation of multiple metabolic proteins with an associated decrease in cellular metabolism, as assessed by lactate and NAD levels. Furthermore, we have also identified the down-regulation of multiple proteasomal subunits, resulting in a significant decrease in 20S proteasome activity. Additionally, we have identified a novel association between Plk1 and p53 through heterogeneous ribonucleoprotein C1/C2 (hnRNPC), thus providing valuable insight into Plk1's role in cancer cell survival.

Indexed as

Cell Cycle ProteinsCell Line, TumorHeterogeneous-Nuclear Ribonucleoprotein Group CHumansMelanomaMutationPolo-Like Kinase 1Proteasome Endopeptidase ComplexProtein Kinase InhibitorsProtein Serine-Threonine KinasesProteomicsProto-Oncogene ProteinsProto-Oncogene Proteins B-rafPteridinesSkin NeoplasmsTandem Mass SpectrometryBI 6727BRAF protein, humanCell Cycle ProteinsHeterogeneous-Nuclear Ribonucleoprotein Group CHNRNPC protein, humanPolo-Like Kinase 1Proteasome Endopeptidase ComplexProtein Kinase InhibitorsProtein Serine-Threonine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins B-rafPteridinesBI 6727glycolysishnRNPCLDHAmelanomap53Plk1polo-like kinase 1proteasomeproteomics

Identifiers

PMID24884503
PMCPMC4227549
OpenAlexW2045726291

What OpenQuestion holds

Textmetadata
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.