Evidence map›Paper›PMID 16465179›Full record

ReviewBritish journal of pharmacology2006

Growth factor signalling in prostatic growth: significance in tumour development and therapeutic targeting.

Arich Ryan Reynolds, Natasha Kyprianou

Open access · bronzeAbstract readReview
In one paragraph

Review in British journal of pharmacology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
  2. Review
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  4. Article
  5. Review
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  9. Review
  10. Article
  11. Article
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  15. Review
  16. Article
  17. Prostate cancer: the need for biomarkers and new therapeutic targets.Journal of Zhejiang University. Science. B · 2014
    Review
  18. Review
  19. Autophagy in prostate cancer and androgen suppression therapy.International journal of molecular sciences · 2013
    Review
  20. Article
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 1 institution in 1 country.

Arich Ryan ReynoldsDepartment of Surgery, University of Kentucky Medical Center, Lexington, KY 40536, USA. nkypr2@uky.edu
Natasha Kyprianou
University of Kentucky · US

Funding

TGF BETA SIGNAL TRANSDUCTION IN PROSTATE CANCERR01DK053525 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI KYPRIANOU, NATASHA · 1997 to 2005
$843k
NIDDK NIH HHS R01 DK053525NIDDK NIH HHS R01 DK53525-06
6 · The paper itself

Abstract

The intricate balance maintained between cell growth and proliferation factors and apoptosis-inducing factors is fundamental to the regulation of prostate growth. Disruptions in this homeostasis often trigger the loss of apoptosis and the over-expression of factors promoting cell survival and proliferation, inevitably leading to tumorigenesis and cancer. Deregulation of prostate growth during prostate cancer development and progression is characterized by apoptotic evasion, uncontrolled proliferation, and increased invasive potential. Thus, in advanced stages of disease progression, surviving prostate tumour cells acquire the ability to migrate and invade heterotopic tissues, with the bone and lymph nodes being the most common sites for human prostate cancer metastasis. The challenges in the implementation of effective therapeutic strategies for the treatment of advanced metastatic prostate cancer reflect the multidimensional nature and functional significance of antiapoptotic pathways in the emergence of therapeutic resistance of prostate tumours. In this chapter, we discuss the current understanding of the molecular mechanisms governing growth factor signalling pathways with often overlapping functions that contribute to loss of apoptosis control and activation of cell proliferation towards aggressive prostate tumorigenic growth and metastatic behaviour. While a full understanding of the prosurvival characteristics of these growth factor pathways is still evolving, the impact that growth factors such a epidermal growth factor and transforming growth factor-beta can be recognized by the vigorous attempts at therapeutic targeting of their key signalling steps.

Indexed as

Signal TransductionAnimalsAntineoplastic AgentsApoptosisCell ProliferationCell Transformation, NeoplasticFibroblast Growth FactorsHumansInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsMaleNeovascularization, PathologicProstateProstatic NeoplasmsTransforming Growth Factor betaVascular Endothelial Growth Factor AAntineoplastic AgentsFibroblast Growth FactorsInsulin-Like Growth Factor IIntercellular Signaling Peptides and ProteinsTransforming Growth Factor betaVascular Endothelial Growth Factor A

Identifiers

PMID16465179
PMCPMC1751493
OpenAlexW2005911388

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.