Evidence map›Paper›PMID 22893202›Full record

ReviewRecent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer2013

New NSAID targets and derivatives for colorectal cancer chemoprevention.

Heather N Tinsley, William E Grizzle, Ashraf Abadi, Adam Keeton, Bing Zhu, Yaguang Xi, Gary A Piazza

Open access · greenAbstract readReview
In one paragraph

Review in Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
17.3field-weighted citation impact, top 1% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
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  16. Novel non-cyclooxygenase inhibitory derivatives of naproxen for colorectal cancer chemoprevention.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2014
    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

7 authors at 5 institutions in 2 countries.

Heather N TinsleyDepartment of Biology, University of Montevallo, Montevallo, AL, USA.
William E Grizzle
Ashraf Abadi
Adam Keeton
Bing Zhu
Yaguang Xi
Gary A Piazza
University of South Alabama · USGerman University in Cairo · EGUniversity of Alabama at Birmingham · USUniversity of Montevallo · USUSA Mitchell Cancer Institute · US

Funding

Selective anti-cancer activity of sulindac derivatives on KRAS mutant colon tumor cells by inducing ROSR01CA131378 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI PIAZZA, GARY A · 2008 to 2019
$5.2M
Development of a novel sulindac amide for colorectal cancer chemopreventionR01CA148817 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI PIAZZA, GARY A · 2010 to 2015
$2.4M
Phosphodiesterase 5: A Novel Target and Inhibitor for Breast Cancer ChemopreventionR01CA155638 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI PIAZZA, GARY A · 2012 to 2017
$2.3M
MicroRNA, sulindac, and breast cancer chemopreventionR21CA160280 · NCI · UNIVERSITY OF SOUTH ALABAMA · PI PIAZZA, GARY A, XI, YAGUANG · 2012 to 2013
$346k
NCI NIH HHS R01 CA131378NCI NIH HHS R01 CA148817NCI NIH HHS R01 CA155638NCI NIH HHS R21 CA160280
6 · The paper itself

Abstract

Clinical and preclinical studies provide strong evidence that nonsteroidal anti-inflammatory drugs (NSAIDs) can prevent numerous types of cancers, especially colorectal cancer. Unfortunately, the depletion of physiologically important prostaglandins due to cyclooxygenase (COX) inhibition results in potentially fatal toxicities that preclude the long-term use of NSAIDs for cancer chemoprevention. While studies have shown an involvement of COX-2 in colorectal tumorigenesis, other studies suggest that a COX-independent target may be at least partially responsible for the antineoplastic activity of NSAIDs. For example, certain NSAID derivatives have been identified that do not inhibit COX-2 but have demonstrated efficacy to suppress carcinogenesis with potential for reduced toxicity. A number of alternative targets have also been reported to account for the tumor cell growth inhibitory activity of NSAIDs, including the inhibition of cyclic guanosine monophosphate phosphodiesterases (cGMP PDEs), generation of reactive oxygen species (ROS), the suppression of the apoptosis inhibitor protein, survivin, and others. Here, we review several promising mechanisms that are being targeted to develop safer and more efficacious NSAID derivatives for colon cancer chemoprevention.

Indexed as

AnimalsAnticarcinogenic AgentsAnti-Inflammatory Agents, Non-SteroidalColorectal NeoplasmsCyclic Nucleotide Phosphodiesterases, Type 2Cyclooxygenase 2 InhibitorsHumansInhibitor of Apoptosis ProteinsReactive Oxygen SpeciesSurvivinAnticarcinogenic AgentsAnti-Inflammatory Agents, Non-SteroidalBIRC5 protein, humanCyclic Nucleotide Phosphodiesterases, Type 2Cyclooxygenase 2 InhibitorsInhibitor of Apoptosis ProteinsReactive Oxygen SpeciesSurvivin

Identifiers

PMID22893202
PMCPMC3703626
OpenAlexW77784348

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.