Evidence map›Paper›PMID 19836385›Full record

ReviewEuropean journal of pharmacology2009

TNF-related apoptosis-inducing ligand (TRAIL): a new path to anti-cancer therapies.

Peter A Holoch, Thomas S Griffith

Abstract readReview
In one paragraph

Review in European journal of pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing 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

93 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Components of the JNK-MAPK pathway play distinct roles in hepatocellular carcinoma.Journal of cancer research and clinical oncology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. TargetingFrontiers in oncology · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Regulation of pancreatic cancer TRAIL resistance by protein O-GlcNAcylation.Laboratory investigation; a journal of technical methods and pathology · 2020
    Article
  17. Review
  18. Article
  19. Article
  20. Article

33 more citing papers are in PubMed but not listed here.

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.

Peter A HolochDepartment of Urology, University of Iowa, 375 Newton Road, Iowa City, IA 52242, USA.
Thomas S Griffith

Funding

TRAIL-expressing Recombinant Adenovirus Based Immunotherapy for RCCR01CA109446 · NCI · UNIVERSITY OF MINNESOTA · PI GRIFFITH, THOMAS S · 2004 to 2013
$2.6M
TNF-related apoptosis-inducing ligan (TRAIL) gene therapy for prostate cancerR21CA110486 · NCI · UNIVERSITY OF IOWA · PI WILLIAMS, RICHARD DWAYNE · 2006 to 2007
$250k
NCI NIH HHS CA109446NCI NIH HHS CA110486NCI NIH HHS R01 CA109446NCI NIH HHS R21 CA110486
6 · The paper itself

Abstract

Since its discovery in 1995, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), a member of the tumor necrosis factor super family, has been under intense focus because of its remarkable ability to induce apoptosis in malignant human cells while leaving normal cells unscathed. Consequently, activation of the apoptotic signaling pathway from the death-inducing TRAIL receptors provides an attractive, biologically-targeted approach to cancer therapy. A great deal of research has focused on deciphering the TRAIL receptor signaling cascade and intracellular regulation of this pathway, as many human tumor cells possess mechanisms of resistance to TRAIL-induced apoptosis. This review focuses on the current state of knowledge regarding TRAIL signaling and resistance, the preclinical development of therapies targeted at TRAIL receptors and modulators of the pathway, and the results of clinical trials for cancer treatment that have emerged from this base of knowledge. TRAIL-based approaches to cancer therapy vary from systemic administration of recombinant, soluble TRAIL protein with or without the combination of traditional chemotherapy, radiation or novel anti-cancer agents to agonistic monoclonal antibodies directed against functional TRAIL receptors to TRAIL gene transfer therapy. A better understanding of TRAIL resistance mechanisms may allow for the development of more effective therapies that exploit this cell-mediated pathway to apoptosis.

Indexed as

AnimalsAntineoplastic AgentsApoptosisClinical Trials as TopicDrug Evaluation, PreclinicalDrug Resistance, NeoplasmGenetic TherapyHumansNeoplasmsSignal TransductionTNF-Related Apoptosis-Inducing LigandAntineoplastic AgentsTNF-Related Apoptosis-Inducing Ligand

Identifiers

PMID19836385
PMCPMC2783837

What OpenQuestion holds

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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.