Evidence map›Paper›PMID 30783186›Full record

ArticleScientific reports2019

Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region.

Hideki Izumi, Yuanyuan Li, Masami Shibaki, Daisuke Mori, Michio Yasunami, Seiji Sato, Hisashi Matsunaga, Takao Mae, Kenji Kodama, Takehiko Kamijo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
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  6. Review
  7. Can CD133 Be Regarded as a Prognostic Biomarker in Oncology: Pros and Cons.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Promotion of cancer cell stemness by Ras.Biochemical Society transactions · 2021
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Cell & bioscience · 2019
    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

12 authors at 2 institutions in 1 country.

Hideki IzumiLaboratory of Molecular Medicine, Life Sciences Institute, Saga Medical Center KOSEIKAN, Saga, 840-8571, Japan. izumi-hideki@koseikan.jp.ORCID 0000-0003-1484-934X
Yuanyuan LiLaboratory of Molecular Medicine, Life Sciences Institute, Saga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Masami ShibakiDepartment of Laboratory Medicine, Saga Medical Center KOSEIKAN, Saga, Japan.
Daisuke MoriDepartment of Laboratory Medicine, Saga Medical Center KOSEIKAN, Saga, Japan.
Michio YasunamiDepartment of Laboratory Medicine, Saga Medical Center KOSEIKAN, Saga, Japan.ORCID 0000-0002-6947-6168
Seiji SatoSaga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Hisashi MatsunagaSaga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Takao MaeSaga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Kenji KodamaSaga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Takehiko KamijoResearch Institute for Clinical Oncology, Saitama Cancer Center, Saitama, 362-0806, Japan.
Yasuhiko KanekoResearch Institute for Clinical Oncology, Saitama Cancer Center, Saitama, 362-0806, Japan.
Akira NakagawaraSaga Medical Center KOSEIKAN, Saga, 840-8571, Japan.
Saga-Ken Medical Centre Koseikan · JPSaitama Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD133 is a transmembranous protein that mainly localises to the plasma membrane in haematopoietic and neural stem cells as well as cancer stem cells. Although CD133 also localises to the cytoplasm, the mechanism of action and function of cytoplasmic CD133 currently remain unknown. We herein demonstrated that when Src family kinase activity is weak, CD133 interacts with HDAC6 and is transported to the pericentrosomal region after internalization and endosome formation via the dynein-based traffic system. Pericentrosomal CD133 is then recycled to the plasma membrane via recycling endosomes. At the pericentrosomal region, endosomal CD133 captures GABARAP, an initiator of autophagy, and inhibits GABARAP-mediated ULK1 activation and the subsequent initiation of autophagy. Furthermore, pericentrosomal CD133 suppresses cell differentiation, such as primary cilium formation and neurite outgrowth, by inhibiting autophagy. Thus, the present results provide evidence to suggest that pericentrosomal CD133 has the unique property of maintaining the undifferentiated status of cells by inhibiting autophagy.

Indexed as

Autophagic Cell DeathAC133 AntigenApoptosis Regulatory ProteinsAutophagy-Related Protein-1 HomologCaco-2 CellsCentrosomeEndosomesHEK293 CellsHumansIntracellular Signaling Peptides and ProteinsMicrotubule-Associated ProteinsAC133 AntigenApoptosis Regulatory ProteinsAutophagy-Related Protein-1 HomologGABARAP protein, humanIntracellular Signaling Peptides and ProteinsMicrotubule-Associated ProteinsPROM1 protein, humanULK1 protein, human

Identifiers

PMID30783186
PMCPMC6381095
OpenAlexW2912478271

What OpenQuestion holds

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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.