Evidence map›Paper›PMID 33947685›Full record

ArticleMolecular cancer therapeutics2021

Combined Inhibition of Rad51 and Wee1 Enhances Cell Killing in HNSCC Through Induction of Apoptosis Associated With Excessive DNA Damage and Replication Stress.

Antje Lindemann, Ameeta A Patel, Lin Tang, Noriaki Tanaka, Frederico O Gleber-Netto, Mason D Bartels, Li Wang, Daniel J McGrail, Shiaw-Yih Lin, Steven J Frank and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. 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
1.6field-weighted citation impact, top 16% 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, 21 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

13 authors at 4 institutions in 2 countries.

Antje Lindemann *Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ameeta A Patel *Department of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Lin TangDepartment of Cellular and Molecular Medicine, The University of Arizona Health Sciences, College of Medicine, Tucson, Arizona.
Noriaki TanakaDepartment of Dentistry and Oral Surgery, Osaka Police Hospital, Osaka, Japan.
Frederico O Gleber-NettoDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-7847-9902
Mason D BartelsDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Li WangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Daniel J McGrailDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Shiaw-Yih LinDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Steven J FrankDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-6517-7884
Mitchell J FrederickDepartment of Otolaryngology-Head and Neck Surgery, Baylor College of Medicine, Houston, Texas.
Jeffrey N Myers *Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas. jmyers@mdanderson.org aaosman@mdanderson.org.ORCID 0000-0003-4767-3408
Abdullah A Osman *Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas. jmyers@mdanderson.org aaosman@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USOsaka Police Hospital · JPUniversity of Arizona · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Targeting replication stress and homologous recombination repair mechanisms in HPV-positive and negative head and neck cancerR01DE030104 · NIDCR · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI FREDERICK, MITCHELL J., OSMAN, ABDULLAH ALI · 2021 to 2025
$1.9M
NCI NIH HHS P30 CA016672NIDCR NIH HHS R01 DE030104
6 · The paper itself

Abstract

Despite advances in surgery, chemotherapy, and radiation, there are limited treatment options for advanced head and neck squamous cell carcinoma (HNSCC) and survival remains very poor. Therefore, effective therapies are desperately needed. Recently, selective exploitation of DNA damage and replication stress responses has become a novel approach for cancer treatment. Wee1 kinase and Rad51 recombinase are two proteins involved in regulating replication stress and homologous recombination repair in cancer cells. In this study, we investigated the combined effect of Rad51 inhibitor (B02) and Wee1 inhibitor (AZD1775)

Indexed as

AnimalsApoptosisCell CycleCell Cycle ProteinsCell Line, TumorCells, CulturedCell SurvivalComputational BiologyDisease Models, AnimalDNA DamageDNA RepairDose-Response Relationship, DrugDrug SynergismGene Expression ProfilingHomologous RecombinationHumansadavosertibCell Cycle ProteinsProtein Kinase InhibitorsProtein-Tyrosine KinasesPyrazolesPyrimidinonesRad51 RecombinaseRadiation-Sensitizing AgentsWEE1 protein, human

Identifiers

PMID33947685
PMCPMC8295235
OpenAlexW3157451023

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.