Evidence map›Paper›PMID 29196475›Full record

ArticleJournal of cell science2017

FYCO1 regulates accumulation of post-mitotic midbodies by mediating LC3-dependent midbody degradation.

Lai Kuan Dionne, Eric Peterman, John Schiel, Paulius Gibieža, Vytenis Arvydas Skeberdis, Antonio Jimeno, Xiao-Jing Wang, Rytis Prekeris

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2017. 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
1.4field-weighted citation impact, top 20% 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, 23 citations in OpenAlex.

  1. Review
  2. Midbody remnant regulates the formation of primary cilia and their roles in tumor growth.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
    Review
  3. Article
  4. Inclusion Body Myositis and Neoplasia: A Narrative Review.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Review
  7. Lysosomes at the Crossroads of Cell Metabolism, Cell Cycle, and Stemness.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. 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

8 authors at 3 institutions in 3 countries.

Lai Kuan DionneDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Eric PetermanDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
John SchielGE Healthcare Dharmacon Inc., 2650 Crescent Drive, Suite 100, Lafayette, CO 80026, USA.
Paulius GibiežaInstitute of Cardiology, Lithuanian University of Health Sciences, Kaunas 50161, Lithuania.
Vytenis Arvydas SkeberdisInstitute of Cardiology, Lithuanian University of Health Sciences, Kaunas 50161, Lithuania.
Antonio JimenoMedical Oncology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Xiao-Jing WangDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA rytis.prekeris@ucdenver.edu xj.wang@ucdenver.edu.
Rytis PrekerisDepartment of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA rytis.prekeris@ucdenver.edu xj.wang@ucdenver.edu.ORCID http://orcid.org/0000-0003-3393-1963
University of Colorado Anschutz Medical Campus · USLithuanian University of Health Sciences · LTGeneral Electric (Spain) · ES

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Molecular Mechanisms Regulating Epithelial Cell Apical Polarity and CiliogenesisR01DK064380 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Rytis Prekeris · 2004 to 2026
$7.1M
Targeting PD-L1 interactome signaling to enhance immunotherapy efficacy in head and neck squamous cell cancerR01CA149456 · NCI · UNIVERSITY OF COLORADO DENVER · PI Antonio Jimeno · 2010 to 2026
$5.6M
Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Role of TGFbeta signaling in HNSCC progressionR01DE015953 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI WANG, XIAO-JING · 2004 to 2014
$3.6M
Identifying oral cancer stem cell properties affected by the microenvironmentR01DE024371 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI JIMENO, ANTONIO, WANG, XIAO-JING · 2014 to 2017
$2.1M
NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA149456NCI NIH HHS T32 CA174648NIDCR NIH HHS R01 DE015953NIDCR NIH HHS R01 DE024371NIDDK NIH HHS R01 DK064380
6 · The paper itself

Abstract

The post-mitotic midbody (MB) is a remnant of cytokinesis that can be asymmetrically inherited by one of the daughter cells following cytokinesis. Until recently, the MB was thought to be degraded immediately following cytokinesis. However, recent evidence suggests that the MB is a protein-rich organelle that accumulates in stem cell and cancer cell populations, indicating that it may have post-mitotic functions. Here, we investigate the role of FYCO1, an LC3-binding protein (herein, LC3 refers to MAP1LC3B), and its function in regulating the degradation of post-mitotic MBs. We show that FYCO1 is responsible for formation of LC3-containing membrane around the post-mitotic MB and that FYCO1 knockdown increases MB accumulation. Although MBs accumulate in the stem-cell-like population of squamous cell carcinomas, FYCO1 depletion does not affect the clonogenicity of these cells. Instead, MB accumulation leads to an increase in anchorage-independent growth and invadopodia formation in HeLa cells and squamous carcinoma cells. Collectively, our data suggest that FYCO1 regulates MB degradation, and we present the first evidence that cancer invasiveness is a feature that can be modulated by the accumulation of MBs in cancer stem cells.This article has an associated First Person interview with the first author of the paper.

Indexed as

AutophagyCell DifferentiationDNA-Binding ProteinsHeLa CellsHumansMicrotubule-Associated ProteinsMicrotubulesOrganellesTranscription FactorsDNA-Binding ProteinsFYCO1 protein, humanMAP1LC3B protein, humanMicrotubule-Associated ProteinsTranscription FactorsAutophagyCytokinesisMidbodyPost-mitotic accumulationPost-mitotic degradation

Identifiers

PMID29196475
PMCPMC5769594
OpenAlexW2774487565

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.