Evidence map›Paper›PMID 7479798›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

Cloning and characterization of a cellular apoptosis susceptibility gene, the human homologue to the yeast chromosome segregation gene CSE1.

U Brinkmann, E Brinkmann, M Gallo, I Pastan

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

60 citing papers in PubMed, 173 citations in OpenAlex.

  1. Review
  2. Mechanism of exportin retention in the cell nucleus.The Journal of cell biology · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
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  9. Article
  10. Circ_cse1l Inhibits Colorectal Cancer Proliferation by Binding to eIF4A3.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. CAS (CSE1L) signaling pathway in tumor progression and its potential as a biomarker and target for targeted therapy.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Immunoconjugates in the management of hairy cell leukemia.Best practice & research. Clinical haematology · 2015
    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

4 authors at 1 institution in 1 country.

U BrinkmannLaboratory of Molecular Biology, National Cancer Institutes, National Institutes of Health, Bethesda, MD 20892-4255, USA.
E Brinkmann
M Gallo
I Pastan
National Institutes of Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We recently isolated human cDNA fragments that render MCF-7 breast cancer cells resistant to cell death caused by Pseudomonas exotoxin, Pseudomonas exotoxin-derived immunotoxins, diphtheria toxin, and tumor necrosis factor. We report here that one of these fragments is an antisense fragment of a gene homologous to the essential yeast chromosome segregation gene CSE1. Cloning and analysis of the full-length cDNA of the human CSE1 homologue, which we name CAS for cellular apoptosis susceptibility gene, reveals a protein coding region with similar length (971 amino acids for CAS, 960 amino acids for CSE1) and 59% overall protein homology to the yeast CSE1 protein. The conservation of this gene indicates it has an important function in human cells consistent with the essential role of CSE1 in yeast. CAS is highly expressed in human tumor cell lines and in human testis and fetal liver, tissues that contain actively dividing cells. Furthermore, CAS expression increases when resting human fibroblasts are induced to proliferate and decreases when they are growth-arrested. Thus, CAS appears to play an important role in both toxin and tumor necrosis factor-mediated cell death, as well as in cell proliferation.

Indexed as

Gene ExpressionGenes, FungalNuclear ProteinsProtein BiosynthesisSaccharomyces cerevisiae ProteinsAmino Acid SequenceApoptosisBreast NeoplasmsCell DivisionCell LineCellular Apoptosis Susceptibility ProteinChromosomes, FungalCloning, MolecularDNA, ComplementaryFemaleFetusCellular Apoptosis Susceptibility ProteinCSE1 protein, S cerevisiaeDNA, ComplementaryFungal ProteinsNuclear ProteinsNucleocytoplasmic Transport ProteinsProteinsRecombinant ProteinsRNA, MessengerSaccharomyces cerevisiae Proteins

Identifiers

PMID7479798
PMCPMC40810
OpenAlexW2043545670

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.