Evidence map›Paper›PMID 33489883›Full record

ArticleFrontiers in oncology2020

MYBL2-Driven Transcriptional Programs Link Replication Stress and Error-prone DNA Repair With Genomic Instability in Lung Adenocarcinoma.

Benjamin B Morris, Nolan A Wages, Patrick A Grant, P Todd Stukenberg, Ryan D Gentzler, Richard D Hall, Wallace L Akerley, Thomas K Varghese, Susanne M Arnold, Terence M Williams and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

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  14. [High expression of MYBL2 promotes progression and predicts a poor survival outcome of prostate cancer].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  15. Frontiers in oncology · 2021
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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

14 authors at 8 institutions in 1 country.

Benjamin B MorrisDepartment of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, United States.
Nolan A WagesDepartment of Public Health Sciences, University of Virginia, Charlottesville, VA, United States.
Patrick A GrantDepartment of Biomedical Science, Florida Atlantic University, Boca Raton, FL, United States.
P Todd StukenbergDepartment of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, United States.
Ryan D GentzlerDivision of Medical Oncology, Department of Internal Medicine, Hematology/Oncology, University of Virginia Health System, Charlottesville, VA, United States.
Richard D HallDivision of Medical Oncology, Department of Internal Medicine, Hematology/Oncology, University of Virginia Health System, Charlottesville, VA, United States.
Wallace L AkerleyDepartment of Medical Oncology, Department of Internal Medicine, Huntsman Cancer Institute, Salt Lake City, UT, United States.
Thomas K VargheseDivision of Thoracic Surgery, Department of Surgery, University of Utah, Salt Lake City, UT, United States.
Susanne M ArnoldDepartment of Internal Medicine, Division of Medical Oncology, Markey Cancer Center, Lexington, KY, United States.
Terence M WilliamsDepartment of Radiation Oncology, The Ohio State University Comprehensive Cancer Center, Columbus, OH, United States.
Vincenzo CoppolaDepartment of Cancer Biology and Genetics, The Ohio State University Comprehensive Cancer Center, Columbus, OH, United States.
David R JonesDepartment of Thoracic Surgery, Memorial Sloan-Kettering Cancer Center, New York, NY, United States.
David T AubleDepartment of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, United States.
Marty W MayoDepartment of Biochemistry & Molecular Genetics, University of Virginia, Charlottesville, VA, United States.
University of Virginia · USThe Ohio State University · USUniversity of Virginia Health System · USFlorida Atlantic University · USHuntsman Cancer Institute · USMarkey Cancer Center · USMemorial Sloan Kettering Cancer Center · USUniversity of Utah · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
BRMS1-mediated suppression of metastases in p53 mutant lung adenocarcinomaR01CA217169 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONES, DAVID R · 2018 to 2022
$2.5M
Targeting SNP BRMS1v2 A273V/A273V to reduce metastases in lung adenocarcinomaR01CA240472 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI JONES, DAVID R · 2019 to 2023
$2.4M
Identifying tumor suppressor targets of SIRT6 in lung cancerR01CA192399 · NCI · UNIVERSITY OF VIRGINIA · PI MAYO, MARTY W · 2015 to 2019
$1.9M
Molecular Mechanisms of Mitotic RegulationR01GM118798 · NIGMS · UNIVERSITY OF VIRGINIA · PI STUKENBERG, P. TODD · 2017 to 2020
$1.8M
Mechanisms to move and steer chromosomesR01GM124042 · NIGMS · UNIVERSITY OF VIRGINIA · PI STUKENBERG, P. TODD · 2018 to 2021
$1.7M
Regulation of a novel epigenome of protein biosynthesis genesR01GM111911 · NIGMS · UNIVERSITY OF VIRGINIA · PI BEKIRANOV, STEFAN, GRANT, PATRICK A · 2015 to 2018
$1.4M
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA044579NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA192399NCI NIH HHS R01 CA217169NCI NIH HHS R01 CA240472NCI NIH HHS T32 CA009109NIGMS NIH HHS R01 GM111911NIGMS NIH HHS R01 GM118798NIGMS NIH HHS R01 GM124042
6 · The paper itself

Abstract

It has long been recognized that defects in cell cycle checkpoint and DNA repair pathways give rise to genomic instability, tumor heterogeneity, and metastasis. Despite this knowledge, the transcription factor-mediated gene expression programs that enable survival and proliferation in the face of enormous replication stress and DNA damage have remained elusive. Using robust omics data from two independent studies, we provide evidence that a large cohort of lung adenocarcinomas exhibit significant genome instability and overexpress the DNA damage responsive transcription factor MYB proto-oncogene like 2 (MYBL2). Across two studies, elevated

Indexed as

error-prone DNA repairhomologous recombination (HR)lung adenocarcinomamicrohomology mediated-end joining repair (MMEJ)MYBL2

Identifiers

PMID33489883
PMCPMC7821388
OpenAlexW3119615461

What OpenQuestion holds

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Registered trials

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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.