Evidence map›Paper›PMID 19555499›Full record

ArticleBMC cell biology2009

Evidence for a mitochondrial localization of the retinoblastoma protein.

Ioana Ferecatu, Nathalie Le Floch, Marie Bergeaud, Aida Rodríguez-Enfedaque, Vincent Rincheval, Lisa Oliver, François M Vallette, Bernard Mignotte, Jean-Luc Vayssière

Abstract read
In one paragraph

Article in BMC cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  5. Mutant huntingtin disrupts mitochondrial proteostasis by interacting with TIM23.Proceedings of the National Academy of Sciences of the United States of America · 2019
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  16. Article
  17. Mitochondrial dysfunction in cancer.Frontiers in oncology · 2013
    Review
  18. Article
  19. Article
  20. 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

9 authors.

Ioana FerecatuLaboratoire de génétique et biologie cellulaire - CNRS UMR 8159, Université de Versailles Saint-Quentin-en-Yvelines, Versailles, France. ioana-costina.parvu@uvsq.fr
Nathalie Le Floch
Marie Bergeaud
Aida Rodríguez-Enfedaque
Vincent Rincheval
Lisa Oliver
François M Vallette
Bernard Mignotte
Jean-Luc Vayssière

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe retinoblastoma protein (Rb) plays a central role in the regulation of cell cycle, differentiation and apoptosis. In cancer cells, ablation of Rb function or its pathway is a consequence of genetic inactivation, viral oncoprotein binding or deregulated hyperphosphorylation. Some recent data suggest that Rb relocation could also account for the regulation of its tumor suppressor activity, as is the case for other tumor suppressor proteins, such as p53.

resultsIn this reported study, we present evidence that a fraction of the total amount of Rb protein can localize to the mitochondria in proliferative cells taken from both rodent and human cells. This result is also supported by the use of Rb siRNAs, which substantially reduced the amount of mitochondrial Rb, and by acellular assays, in which [35S]-Methionine-labeled Rb proteins bind strongly to mitochondria isolated from rat liver. Moreover, endogenous Rb is found in an internal compartment of the mitochondria, within the inner-membrane. This is consistent with the protection of Rb from alkaline treatment, which destroys any interaction of proteins that are weakly bound to mitochondria.

conclusionAlthough a few data regarding an unspecific cytosolic localization of Rb protein have been reported for some tumor cells, our results are the first evidence of a mitochondrial localization of Rb. The mitochondrial localization of Rb is observed in parallel with its classic nuclear location and paves the way for the study of potential as-yet-unknown roles of Rb at this site.

Indexed as

AnimalsApoptosisCell FractionationCell LineHumansMiceMitochondriaRatsRetinoblastoma ProteinRetinoblastoma Protein

Identifiers

PMID19555499
PMCPMC2711044

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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.