Evidence map›Paper›PMID 42602968›Full record

ArticleiScience2026

The Odf2 status contributes to asymmetric inheritance of CD133-positive recycling endosomes during cytokinesis in SK-N-DZ human neuroblastoma cells.

Hideki Izumi, Takao Mae, Sachiko Tsukita, Akira Nakagawara

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Hideki IzumiLaboratory of Molecular Medicine, Medical Research Institute, Saga Medical Center KOSEIKAN, Saga, Japan.
Takao MaeSaga Medical Center KOSEIKAN, Saga, Japan.
Sachiko TsukitaAdvanced Comprehensive Research Organization, Teikyo University, Tokyo, Japan.
Akira NakagawaraSaga HIMAT, Tosu, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asymmetric cell division (ACD) is a physiological event that maintains development and tissue homeostasis. ACD generates two unequal daughter cells, one of which has stem cell properties while the other has differentiation potential. Recent studies show that the balance between self-renewal and differentiation is precisely controlled and that the disruption of this balance leads to diseases, such as tumors. Herein, we examined centrosome inheritance during cell division by using the human neuroblastoma cell line SK-N-DZ. The results showed that daughter cells inheriting daughter centrosomes with younger mother centrioles received more CD133-recycling endosomes, while those inheriting mother centrosomes with older mother centrioles received fewer CD133-recycling endosomes. The depletion of outer dense fiber protein 2/cenexin, which localizes to both centrosomal distal and subdistal appendages, strongly promoted the localization of recycling endosomes at both centrosomes, and ACD was lost. Therefore, these results may facilitate further research on the mechanisms underlying centrosome inheritance in ACD.

Indexed as

asymmetric cell divisionCD133centrosomeneuroblastomaOdf2recycling endosome

Identifiers

PMID42602968
PMCPMC13475681

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.