Evidence map›Paper›PMID 20013032›Full record

ReviewCancer metastasis reviews2009

Phosphatidylinositol 3-kinase (PI3K) pathway activation in bladder cancer.

Margaret A Knowles, Fiona M Platt, Rebecca L Ross, Carolyn D Hurst

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer metastasis reviews, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

90 citing papers in PubMed, 162 citations in OpenAlex.

  1. Article
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  5. Review
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  15. Article
  16. Review
  17. Article
  18. AR and PI3K/AKT in Prostate Cancer: A Tale of Two Interconnected Pathways.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review

30 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

4 authors at 2 institutions in 1 country.

Margaret A KnowlesCancer Research UK Clinical Centre, Leeds Institute of Molecular Medicine, St James's University Hospital, Beckett Street, Leeds LS9 7TF, UK. M.A.Knowles@leeds.ac.uk
Fiona M Platt
Rebecca L Ross
Carolyn D Hurst
St James's University Hospital · GBCancer Research UK · GB

Funding

Cancer Research UK C6228/A5437Medical Research Council
6 · The paper itself

Abstract

The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.

Indexed as

Antineoplastic AgentsCarcinoma in SituCarcinoma, PapillaryCarcinoma, Transitional CellCell Transformation, NeoplasticDrug Delivery SystemsEnzyme ActivationHumansHyperplasiaModels, BiologicalMutationNeoplasm ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseReceptor Protein-Tyrosine KinasesAKT1 protein, humanAntineoplastic AgentsNeoplasm ProteinsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanReceptor Protein-Tyrosine KinasesTSC1 protein, humanTuberous Sclerosis Complex 1 ProteinTumor Suppressor Proteins

Identifiers

PMID20013032
PMCPMC2797439
OpenAlexW2162532809

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.