Evidence map›Paper›PMID 36695333›Full record

ArticleJournal of cell science2023

CCDC86 is a novel Ki-67-interacting protein important for cell division.

Konstantinos Stamatiou, Aldona Chmielewska, Shinya Ohta, William C Earnshaw, Paola Vagnarelli

Open access · hybridFull text read
In one paragraph

Article in Journal of cell science, 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
1.5field-weighted citation impact, top 18% 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, 10 citations in OpenAlex.

  1. Article
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  7. Review
  8. Comparative Review of the Conserved UL24 Protein Family in Herpesviruses.International journal of molecular sciences · 2024
    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 3 institutions in 2 countries.

Konstantinos StamatiouCollege of Health, Medicine and Life Sciences, Department of Life Sciences, Brunel University London, London UB8 3PH, UK.ORCID 0000-0002-5650-078X
Aldona ChmielewskaWellcome Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh EH16 4SB, UK.ORCID 0000-0003-3411-6776
Shinya OhtaInstitute for Genetic Medicine, Hokkaido University, Kita-15, Nishi-7, Kita-Ku, Sapporo 060-0815, Japan.ORCID 0000-0003-2424-1741
William C EarnshawWellcome Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh EH16 4SB, UK.ORCID 0000-0002-7191-0621
Paola VagnarelliCollege of Health, Medicine and Life Sciences, Department of Life Sciences, Brunel University London, London UB8 3PH, UK.ORCID 0000-0002-0000-2271
Brunel University of London · GBWellcome Centre for Cell Biology · GBHokkaido University · JP

Funding

Wellcome Trust 107022Wellcome Trust 210742/Z/18/Z
6 · The paper itself

Abstract

The chromosome periphery is a network of proteins and RNAs that coats the outer surface of mitotic chromosomes. Despite the identification of new components, the functions of this complex compartment are poorly characterised. In this study, we identified a novel chromosome periphery-associated protein, CCDC86 (also known as cyclon). Using a combination of RNA interference, microscopy and biochemistry, we studied the functions of CCDC86 in mitosis. CCDC86 depletion resulted in partial disorganisation of the chromosome periphery with alterations in the localisation of Ki-67 (also known as MKI67) and nucleolin (NCL), and the formation of abnormal cytoplasmic aggregates. Furthermore, CCDC86-depleted cells displayed errors in chromosome alignment, altered spindle length and increased apoptosis. These results suggest that, within the chromosome periphery, different subcomplexes that include CCDC86, nucleolin and B23 (nucleophosmin or NPM1) are required for mitotic spindle regulation and correct kinetochore-microtubule attachments, thus contributing to chromosome segregation in mitosis. Moreover, we identified CCDC86 as a MYCN-regulated gene, the expression levels of which represent a powerful marker for prognostic outcomes in neuroblastoma.

Indexed as

MitosisSpindle ApparatusChromosomesChromosome SegregationHeLa CellsHumansKi-67 AntigenKinetochoresMicrotubulesKi-67 AntigenCCDC86Cell divisionChromosomesKi-67MYCN

Identifiers

PMID36695333
PMCPMC10022746
OpenAlexW4317934058

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read32
identifiers read1
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.