Evidence map›Paper›PMID 37584777›Full record

ArticleCellular and molecular life sciences : CMLS2023

AMBRA1 phosphorylation by CDK1 and PLK1 regulates mitotic spindle orientation.

Fiorella Faienza, Federica Polverino, Girish Rajendraprasad, Giacomo Milletti, Zehan Hu, Barbara Colella, Deborah Gargano, Flavie Strappazzon, Salvatore Rizza, Mette Vixø Vistesen and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. CDK4/6 Inhibitors Impede Chemoresistance and Inhibit Tumor Growth of Small Cell Lung Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  9. Unveiling the Paradoxical Nature of Autophagy in Cancer Cell Fate.Cancer control : journal of the Moffitt Cancer Center
    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

22 authors at 12 institutions in 5 countries.

Fiorella FaienzaCell Stress and Survival Group, Center for Autophagy, Recycling and Disease (CARD), Danish Cancer Institute, Copenhagen, Denmark.
Federica PolverinoInstitute of Molecular Biology and Pathology, CNR National Research Council, Rome, Italy.
Girish RajendraprasadCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.
Giacomo MillettiDepartment of Pediatric Hemato-Oncology and Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Zehan HuDepartment of Biology, University of Fribourg, Fribourg, Switzerland.
Barbara ColellaDepartment of Biosciences and Territory, University of Molise, Pesche, Italy.
Deborah GarganoDepartment of Biosciences and Territory, University of Molise, Pesche, Italy.
Flavie StrappazzonIRCCS Fondazione Santa Lucia, Rome, Italy.
Salvatore RizzaRedox Biology Group, Danish Cancer Institute, Copenhagen, Denmark.
Mette Vixø VistesenCell Stress and Survival Group, Center for Autophagy, Recycling and Disease (CARD), Danish Cancer Institute, Copenhagen, Denmark.
Yonglun LuoLars Bolund Institute of Regenerative Medicine and Qingdao-Europe Advanced Institute for Life Sciences, BGI Research, Shenzhen, China.
Manuela AntonioliDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Valentina CianfanelliDepartment of Pediatric Hemato-Oncology and Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Caterina FerrainaDepartment of Pediatric Hemato-Oncology and Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Gian Maria FimiaNational Institute for Infectious Diseases, IRCSS "L. Spallanzani", Rome, Italy.
Giuseppe FilomeniDepartment of Biology, University of Rome Tor Vergata, Rome, Italy.
Daniela De ZioMelanoma Research Team, Danish Cancer Institute, Copenhagen, Denmark.
Joern DengjelDepartment of Biology, University of Fribourg, Fribourg, Switzerland.
Marin BarisicCell Division and Cytoskeleton, Danish Cancer Institute, Copenhagen, Denmark.
Giulia GuarguagliniInstitute of Molecular Biology and Pathology, CNR National Research Council, Rome, Italy.
Sabrina Di BartolomeoDepartment of Biosciences and Territory, University of Molise, Pesche, Italy. sabrina.dibartolomeo@unimol.it.
Francesco CecconiCell Stress and Survival Group, Center for Autophagy, Recycling and Disease (CARD), Danish Cancer Institute, Copenhagen, Denmark. cecconi@cancer.dk.ORCID http://orcid.org/0000-0002-5614-4359
University of Molise · ITUniversity of Rome Tor Vergata · ITBambino Gesù Children's Hospital · ITDanish Cancer Society · DKInstitute of Molecular Biology and Pathology · ITUniversity of Copenhagen · DKUniversity of Fribourg · CHAarhus University · DKIstituto Nazionale per le Malattie Infettive Lazzaro Spallanzani · ITRoma Tre University · ITUniversità Cattolica del Sacro Cuore · ITUniversité Claude Bernard Lyon 1 · FR

Funding

Associazione Italiana per la Ricerca sul Cancro 23543Kræftens Bekæmpelse R146-A9364Kræftens Bekæmpelse R72-A4408LEO Fondet LF17024Lundbeckfonden R233-2016-3360Novo Nordisk Fonden 22544Novo Nordisk Fonden 7559
6 · The paper itself

Abstract

AMBRA1 is a crucial factor for nervous system development, and its function has been mainly associated with autophagy. It has been also linked to cell proliferation control, through its ability to regulate c-Myc and D-type cyclins protein levels, thus regulating G1-S transition. However, it remains still unknown whether AMBRA1 is differentially regulated during the cell cycle, and if this pro-autophagy protein exerts a direct role in controlling mitosis too. Here we show that AMBRA1 is phosphorylated during mitosis on multiple sites by CDK1 and PLK1, two mitotic kinases. Moreover, we demonstrate that AMBRA1 phosphorylation at mitosis is required for a proper spindle function and orientation, driven by NUMA1 protein. Indeed, we show that the localization and/or dynamics of NUMA1 are strictly dependent on AMBRA1 presence, phosphorylation and binding ability. Since spindle orientation is critical for tissue morphogenesis and differentiation, our findings could account for an additional role of AMBRA1 in development and cancer ontogenesis.

Indexed as

Protein Serine-Threonine KinasesSpindle ApparatusAdaptor Proteins, Signal TransducingCDC2 Protein KinaseCell CycleCell Cycle ProteinsHeLa CellsHumansMitosisPhosphorylationAdaptor Proteins, Signal TransducingAMBRA1 protein, humanCDC2 Protein KinaseCDK1 protein, humanCell Cycle ProteinsProtein Serine-Threonine KinasesCell cycleMitotic kinasesMitotic spindleNUMA1Phosphorylation

Identifiers

PMID37584777
PMCPMC10432340
OpenAlexW4385851003

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.