Evidence map›Paper›PMID 35463312›Full record

ReviewFrontiers in oncology2022

Recent Advances in the Development of Non-PIKKs Targeting Small Molecule Inhibitors of DNA Double-Strand Break Repair.

Jeremy M Kelm, Amirreza Samarbakhsh, Athira Pillai, Pamela S VanderVere-Carozza, Hariprasad Aruri, Deepti S Pandey, Katherine S Pawelczak, John J Turchi, Navnath S Gavande

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2022. 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
2.0field-weighted citation impact, top 13% 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, 23 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

9 authors at 6 institutions in 1 country.

Jeremy M KelmDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Amirreza SamarbakhshDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Athira PillaiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Pamela S VanderVere-CarozzaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Hariprasad AruriDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Deepti S PandeyDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Katherine S PawelczakNERx Biosciences, Indianapolis, IN, United States.
John J TurchiDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United States.
Navnath S GavandeDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, Detroit, MI, United States.
Wayne State University · USEugene Applebaum College of Pharmacy and Health Sciences · USIndiana University – Purdue University Indianapolis · USIndiana University School of MedicineNĒRx BioSciences (United States) · USThe Barbara Ann Karmanos Cancer Institute · US

Funding

Discovery and development of Ku-targeted small molecule inhibitors: A novel mechanism of DNA-PK inhibitionR01CA247370 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI Navnath S Gavande, JOHN J. TURCHI · 2020 to 2026
$3.5M
Novel DNA damage response therapeutics targeting replication protein AR01CA257430 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI TURCHI, JOHN J. · 2021 to 2025
$2.4M
NCI NIH HHS R01 CA247370NCI NIH HHS R01 CA257430
6 · The paper itself

Abstract

The vast majority of cancer patients receive DNA-damaging drugs or ionizing radiation (IR) during their course of treatment, yet the efficacy of these therapies is tempered by DNA repair and DNA damage response (DDR) pathways. Aberrations in DNA repair and the DDR are observed in many cancer subtypes and can promote

Indexed as

DNA double-strand break (DSB) repairDNA repair and DNA damage response (DDR)homology directed repair (HDR)non-homologous end joining (NHEJ)non-PIKKs inhibitorspolymerase theta-mediated end joining (TMEJ)single-strand annealing (SSA)synthetic lethality

Identifiers

PMID35463312
PMCPMC9020266
OpenAlexW4226287293

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.