Evidence map›Paper›PMID 24222103›Full record

ReviewAnticancer research2013

Therapeutic value of quinazoline-based compounds in prostate cancer.

Johnathan Bilbro, Matthew Mart, Natasha Kyprianou

Open access · greenAbstract readReview
In one paragraph

Review in Anticancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 33 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Johnathan BilbroCombs Res. Bldg., Rm. 306, University of Kentucky Medical Center, Lexington, KY 40536, U.S.A. nkypr2@uky.edu.
Matthew Mart
Natasha Kyprianou
University of Kentucky · US

Funding

Anoikis Effect by Quinazolines on Prostate GrowthR01CA107575 · NCI · UNIVERSITY OF KENTUCKY · PI KYPRIANOU, NATASHA · 2004 to 2008
$1.2M
NCI NIH HHS R01 CA107575NCI NIH HHS R01CA107575-6
6 · The paper itself

Abstract

Certain α1-adrenoreceptor antagonists induce significant apoptosis and impair tumor vascularity without affecting cellular proliferation, effects specific to the quinazoline structure. These anticancer effects have been attributed to both induction of classical apoptosis and reversal of anoikis resistance via disruption of integrin-mediated cell survival pathways. Recent drug optimization efforts have generated several novel compounds with quinazoline-derived chemical structure that exert potent anti-tumor activity via anoikis. Results from pre-clinical and clinical studies implicate a potential value of quinazoline-based analogues in prostate cancer prevention and therapy. A retrospective study of a large patient cohort at our center, revealed that treatment with α1-andrenoreceptor antagonists significantly reduced the risk of developing prostate cancer, indicating a potential chemopreventative mechanism for these FDA-approved agents. In the present review we discuss the current understanding of the signaling mechanisms reversing anoikis resistance by the quinazoline-based compounds in prostate tumors, towards enabling identification of novel therapeutic targets for the treatment of metastatic castration-resistant prostate cancer (CRPC).

Indexed as

AnimalsHumansMaleProstatic NeoplasmsQuinazolinesQuinazolinesanoikisdoxazosinDZ-50prostate cancerQuinazolinereviewterazosinvascularity

Identifiers

PMID24222103
PMCPMC5451155
OpenAlexW1848218163

What OpenQuestion holds

Textmetadata
LicenceTDM
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.