Evidence map›Paper›PMID 12606722›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

The p53-inducible TSAP6 gene product regulates apoptosis and the cell cycle and interacts with Nix and the Myt1 kinase.

Brent J Passer, Vanessa Nancy-Portebois, Nathalie Amzallag, Sylvie Prieur, Christophe Cans, Aude Roborel de Climens, Giusy Fiucci, Veronique Bouvard, Marcel Tuynder, Laurent Susini and 7 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

55 citing papers in PubMed, 136 citations in OpenAlex.

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  13. Strategies for Engineering of Extracellular Vesicles.International journal of molecular sciences · 2023
    Review
  14. Red Blood Cell Omics and Machine Learning in Transfusion Medicine: Singularity Is Near.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2023
    Review
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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

17 authors at 4 institutions in 2 countries.

Brent J PasserMolecular Engines Laboratories, 20 Rue Bouvier, 75011 Paris, France.
Vanessa Nancy-Portebois
Nathalie Amzallag
Sylvie Prieur
Christophe Cans
Aude Roborel de Climens
Giusy Fiucci
Veronique Bouvard
Marcel Tuynder
Laurent Susini
Stéphanie Morchoisne
Virginie Crible
Alexandra Lespagnol
Jean Dausset
Moshe Oren
Robert Amson
Adam Telerman
Molecular Engines Laboratories (France) · FRWeizmann Institute of Science · ILFondation Jean Dausset-CEPH · FRHôpital Pontchaillou · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The p53 tumor suppressor protein plays a crucial role in tumorigenesis by controlling cell-cycle progression and apoptosis. We have previously described a transcript designated tumor suppressor activated pathway-6 (TSAP6) that is up-regulated in the p53-inducible cell line, LTR6. Cloning of the murine and human full-length TSAP6 cDNA revealed that it encodes a 488-aa protein with five to six transmembrane domains. This gene is the murine and human homologue of the recently published rat pHyde. Antibodies raised against murine and human TSAP6 recognize a 50- to 55-kDa band induced by p53. Analysis of the TSAP6 promoter identified a functional p53-responsive element. Functional studies demonstrated that TSAP6 antisense cDNA diminished levels of the 50- to 55-kDa protein and decreased significantly the levels of p53-induced apoptosis. Furthermore, TSAP6 small interfering RNA inhibited apoptosis in TSAP6-overexpressing cells. Yeast two-hybrid analysis followed by GST/in vitro-transcribed/translated pull-down assays and in vivo coimmunoprecipitations revealed that TSAP6 associated with Nix, a proapoptotic Bcl-2-related protein and the Myt1 kinase, a negative regulator of the G(2)/M transition. Moreover, TSAP6 enhanced the susceptibility of cells to apoptosis and cooperated with Nix to exacerbate this effect. Cell-cycle studies indicated that TSAP6 could augment Myt1 activity. Overall, these data suggest that TSAP6 may act downstream to p53 to interface apoptosis and cell-cycle progression.

Indexed as

ApoptosisOncogene ProteinsProto-Oncogene ProteinsTumor Suppressor ProteinsAmino Acid SequenceAnimalsBlotting, NorthernBlotting, WesternCell CycleCell Cycle ProteinsCloning, MolecularDNA, ComplementaryFlow CytometryG1 PhaseG2 PhaseGlutathione TransferaseBNIP3L protein, humanCell Cycle ProteinsDNA, ComplementaryGlutathione TransferaseLuciferasesMembrane ProteinsMyt1 kinase, ratOligonucleotides, AntisenseOncogene ProteinsOxidoreductasesPKMYT1 protein, humanProtein Serine-Threonine KinasesProtein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2Recombinant Fusion ProteinsRNA, MessengerRNA, Small InterferingSTEAP3 protein, humanTSAP6 protein, mouseTumor Suppressor Protein p53Tumor Suppressor Proteins

Identifiers

PMID12606722
PMCPMC151332
OpenAlexW2101148281

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.