Evidence map›Paper›PMID 17136319›Full record

ArticleApoptosis : an international journal on programmed cell death2007

Down-regulation of cFLIP following reovirus infection sensitizes human ovarian cancer cells to TRAIL-induced apoptosis.

Penny Clarke, Kenneth L Tyler

Abstract read
In one paragraph

Article in Apoptosis : an international journal on programmed cell death, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

13 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Oncolytic virus therapy for cancer.Oncolytic virotherapy · 2013
    Review
  9. Oncolytic virotherapy for ovarian cancer.Oncolytic virotherapy · 2012
    Article
  10. Targeted ovarian cancer treatment: the TRAILs of resistance.American journal of cancer research · 2012
    Article
  11. Article
  12. Article
  13. 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

2 authors at 2 institutions in 1 country.

Penny ClarkeDepartment of Neurology, University of Colorado Health Sciences Center, 4200 East 9th Avenue, Box B182, Denver, Colorado 80262, USA. penny.clarke@uchsc.edu
Kenneth L Tyler
University of Colorado Health · USVeterans Health Administration · US

Funding

Mechanisms of Apoptosis in the central nervous systemR01NS050138 · NINDS · UNIVERSITY OF COLORADO DENVER · PI TYLER, KENNETH L. · 2005 to 2009
$1.3M
Mechanisms of virus-induced apoptosis in neurons and CNSR01NS051403 · NINDS · UNIVERSITY OF COLORADO DENVER · PI TYLER, KENNETH L. · 2006 to 2010
$1.2M
NINDS NIH HHS 1R01NS051403NINDS NIH HHS 5R01NS050138NINDS NIH HHS R01 NS050138NINDS NIH HHS R01 NS051403
6 · The paper itself

Abstract

Tumor necrosis factor-related apoptosis inducing ligand (TRAIL) shows promise as a chemotherapeutic agent. However, many human cancer cells are resistant to killing by TRAIL. We have previously demonstrated that reovirus infection increases the susceptibility of human lung (H157) and breast (ZR75-1) cancer cell lines to TRAIL-induced apoptosis. We now show that reovirus also increases the susceptibility of human ovarian cancer cell lines (OVCAR3, PA-1 and SKOV-3) to TRAIL-induced apoptosis. Reovirus-induced increases in susceptibility of OVCAR3 cells to TRAIL require virus uncoating and involve increased activation of caspases 3 and 8. Reovirus infection results in the down-regulation of cFLIP (cellular FLICE inhibitory protein) in OVCAR3 cells. Down-regulation of cFLIP following treatment of OVCAR3 cells with antisense cFLIP oligonucleotides or PI3 kinase inhibition also increases the susceptibility of OVCAR3 cells to TRAIL-induced apoptosis. Finally, over-expression of cFLIP blocks reovirus-induced sensitization of OVCAR3 cells to TRAIL-induced apoptosis. The combination of reovirus and TRAIL thus represents a promising new therapeutic approach for the treatment of ovarian cancer.

Indexed as

ApoptosisCASP8 and FADD-Like Apoptosis Regulating ProteinCaspase 8Cell Line, TumorDown-RegulationFemaleHumansMammalian orthoreovirus 3MitochondriaOvarian NeoplasmsRecombinant ProteinsReoviridae InfectionsSignal TransductionTNF-Related Apoptosis-Inducing LigandCASP8 and FADD-Like Apoptosis Regulating ProteinCASP8 protein, humanCaspase 8CFLAR protein, humanRecombinant ProteinsTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, human

Identifiers

PMID17136319
PMCPMC2365758
OpenAlexW2008796901

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.