Evidence map›Paper›PMID 19519210›Full record

ReviewFuture oncology (London, England)2009

Small-molecule inhibitors of proteins involved in base excision repair potentiate the anti-tumorigenic effect of existing chemotherapeutics and irradiation.

April M Reed, Melissa L Fishel, Mark R Kelley

Open access · greenAbstract readReview
In one paragraph

Review in Future oncology (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

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  9. Pro-apoptotic effects of rHSG on C6 glioma cells.International journal of molecular medicine · 2016
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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.

April M ReedDepartment of Pediatrics, Section of Hematology/Oncology, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Melissa L Fishel
Mark R Kelley
Indiana University – Purdue University Indianapolis · US

Funding

The Role of Ape1 in Neurotoxicity of Cancer TreatmentsR01CA121168 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI KELLEY, MARK R. · 2008 to 2012
$2.4M
Imbalancing DNA BER to enhance Ovarian Tumor SensitivityR01CA106298 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KELLEY, MARK R. · 2004 to 2008
$1.5M
Mechanism of Redox Regulation by Ape1/Ref-1R01CA114571 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI GEORGIADIS, MILLIE M · 2006 to 2010
$1.2M
Therapeutic/Mechanistic Role of Ape1 in Germ Cell TumorsR01CA094025 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KELLEY, MARK R. · 2003 to 2007
$1.1M
Chemosensitization of Pancreatic Tumors via Inhibition of a DNA BER Enzyme, Ape1R21CA122298 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FISHEL, MELISSA L. · 2007 to 2008
$333k
NCI NIH HHS CA106298NCI NIH HHS CA114571NCI NIH HHS CA121168NCI NIH HHS CA122298NCI NIH HHS CA94025NCI NIH HHS R01 CA094025NCI NIH HHS R01 CA106298NCI NIH HHS R01 CA114571NCI NIH HHS R01 CA121168NCI NIH HHS R21 CA122298
6 · The paper itself

Abstract

There has been a recent upsurge in the development of small-molecule inhibitors specific to DNA repair proteins or proteins peripherally involved in base excision repair and the DNA damage response. These specific, nominally toxic inhibitors are able to potentiate the effect of existing cancer cell treatments in a wide array of cancers. One of the largest obstacles to overcome in the treatment of cancer is incomplete killing with initial cancer treatments, leading to resistant cancer. The progression of our understanding of cancer and normal cell responses to DNA damage has allowed us to develop biomarkers that we can use to help us predict responses of cancers, more specifically target cancer cells and overcome resistance. Initial successes using these small-molecule DNA repair inhibitors in target-validation experiments and in the early stages of clinical trials indicate an important role for these inhibitors, and allow for the possibility of a future in which cancers are potentially treated in a highly specific, individual manner.

Indexed as

AnimalsAntineoplastic AgentsClinical Trials as TopicDNA RepairHumansNeoplasmsRadiotherapyAntineoplastic Agents

Identifiers

PMID19519210
PMCPMC2756177
OpenAlexW2141806630

What OpenQuestion holds

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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.