Evidence map›Paper›PMID 27384589›Full record

ReviewBiomolecules2016

Turning on the Radio: Epigenetic Inhibitors as Potential Radiopriming Agents.

Bryan Oronsky, Jan Scicinski, Michelle M Kim, Pedro Cabrales, Michael E Salacz, Corey A Carter, Neil Oronsky, Harry Lybeck, Michelle Lybeck, Christopher Larson and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 11 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

12 authors at 6 institutions in 2 countries.

Bryan OronskyEpicentRx, Inc, Mountain View, CA 94040, USA. boronsky@epicentrx.com.
Jan ScicinskiEpicentRx, Inc, Mountain View, CA 94040, USA. jscicinski@epicentrx.com.
Michelle M KimDepartment of Radiation Oncology, University of Michigan, Ann Arbor, MI 48109, USA. michekim@med.umich.edu.
Pedro CabralesDepartment of Bioengineering UCSD, La Jolla, San Diego, CA 92093, USA. pcabrales@ucsd.edu.
Michael E SalaczKU Medical Center, Kansas University, Kansas City, KS 66160, USA. msalacz@kumc.edu.
Corey A CarterMurtha Cancer Center, Walter Reed National Military Medical Center, Bethesda, MD 20889, USA. corey.carter33@gmail.com.
Neil OronskyCFLS Data, Mountain View, CA 94040, USA. nco@cflsdata.com.
Harry LybeckDepartment of Physiology, Helsinki University, 00100 Helsinki, Finland. harrylybeck@gmail.com.
Michelle LybeckEpicentRx, Inc, Mountain View, CA 94040, USA. lybeck.michelle@gmail.com.
Christopher LarsonMoores Cancer Center, UCSD, La Jolla, CA 92093, USA. chris.larson.mail@gmail.com.
Tony R ReidMoores Cancer Center, UCSD, La Jolla, CA 92093, USA. tonyreid@ucsd.edu.
Arnold OronskyInterWest Partners, Menlo Park, CA 94025, USA. AOronsky@interwest.com.
Moores Cancer CenterLa Jolla Bioengineering Institute · USUniversity of Helsinki · FIUniversity of Kansas Medical Center · USUniversity of Michigan · USWalter Reed National Military Medical Center · US

Funding

Attenuating the Oxidative and Myocardial Toxicity of Polymerized HemoglobinsR56HL123015 · NHLBI · OHIO STATE UNIVERSITY · PI CABRALES, PEDRO, PALMER, ANDRE FRANCIS · 2014 to 2014
$400k
NHLBI NIH HHS R56 HL123015
6 · The paper itself

Abstract

First introduced during the late 1800s, radiation therapy is fundamental to the treatment of cancer. In developed countries, approximately 60% of all patients receive radiation therapy (also known as the sixty percenters), which makes radioresistance in cancer an important and, to date, unsolved, clinical problem. Unfortunately, the therapeutic refractoriness of solid tumors is the rule not the exception, and the ubiquity of resistance also extends to standard chemotherapy, molecularly targeted therapy and immunotherapy. Based on extrapolation from recent clinical inroads with epigenetic agents to prime refractory tumors for maximum sensitivity to concurrent or subsequent therapies, the radioresistant phenotype is potentially reversible, since aberrant epigenetic mechanisms are critical contributors to the evolution of resistant subpopulations of malignant cells. Within the framework of a syllogism, this review explores the emerging link between epigenetics and the development of radioresistance and makes the case that a strategy of pre- or co-treatment with epigenetic agents has the potential to, not only derepress inappropriately silenced genes, but also increase reactive oxygen species production, resulting in the restoration of radiosensitivity.

Indexed as

Epigenesis, GeneticHumansNeoplasmsRadiation ToleranceDNA methyltransferase inhibitionepigenetic primingepigeneticshistone deacetylase inhibitionradiosensitizationradiotherapyreactive oxygen species (ROS)

Identifiers

PMID27384589
PMCPMC5039418
OpenAlexW2468752500

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.