Evidence map›Paper›PMID 24154874›Full record

ArticleCancer research2013

APOBEC3B upregulation and genomic mutation patterns in serous ovarian carcinoma.

Brandon Leonard, Steven N Hart, Michael B Burns, Michael A Carpenter, Nuri A Temiz, Anurag Rathore, Rachel I Vogel, Jason B Nikas, Emily K Law, William L Brown and 24 more

Abstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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

119 citing papers in PubMed, 1 synthesis or guideline pooled it, 178 citations in OpenAlex.

  1. Pooled it
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  15. Evolvability of cancer-associated genes under APOBEC3A/B selection.bioRxiv : the preprint server for biology · 2023
    Article
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59 more citing papers are in PubMed but not listed here.

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

34 authors at 2 institutions in 1 country.

Brandon LeonardAuthors' Affiliations: Biochemistry, Molecular Biology and Biophysics Department; Masonic Cancer Center, University of Minnesota, Minneapolis; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research; Medical Genome Facility and Department of Laboratory Medicine and Pathology; Department of Laboratory Medicine and Pathology; Division of Medical Oncology, Department of Oncology; Division of Epidemiology, Department of Health Sciences Research; Division of Oncology Research, Department of Oncology; Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic; Women's Cancer Program, Mayo Clinic Cancer Center, Rochester, Minnesota; Department of Cancer Biology, University of Kansas, Kansas City, Kansas; Department of Obstetrics & Gynecology, University of Washington School of Medicine, Seattle, Washington; and Illumina Cambridge Ltd, Chesterford Research Park, Little Chesterford, Cambridge, United Kingdom.
Steven N Hart
Michael B Burns
Michael A Carpenter
Nuri A Temiz
Anurag Rathore
Rachel I Vogel
Jason B Nikas
Emily K Law
William L Brown
Ying Li
Yuji Zhang
Matthew J Maurer
Ann L Oberg
Julie M Cunningham
Viji Shridhar
Debra A Bell
Craig April
David Bentley
Marina Bibikova
R Keira Cheetham
Jian-Bing Fan
Russell Grocock
Sean Humphray
Zoya Kingsbury
John Peden
Jeremy Chien
Elizabeth M Swisher
Lynn C Hartmann
Kimberly R Kalli
Ellen L Goode
Hugues Sicotte
Scott H Kaufmann
Reuben S Harris
University of Minnesota · USMayo Clinic · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
Use of microfluidic tumor cultures to enable clinical trials of therapies for ovarian cancerP50CA136393 · NCI · MAYO CLINIC ROCHESTER · PI Zhenkun Lou · 2009 to 2026
$37.0M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
Structural Characterization of APOBECS's Atomic interactionsP01GM091743 · NIGMS · UNIVERSITY OF MINNESOTA · PI MATSUO, HIROSHI · 2011 to 2015
$10.1M
UNIVERSITY OF MINNESOTA CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE (UMN CTSI)UL1RR033183 · NCRR · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2011 to 2011
$8.9M
APOBEC proteins and uracil in retrovirus restrictionR01AI064046 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HARRIS, REUBEN S · 2005 to 2014
$3.0M
Genetic Variation in the NF-kappaB Pathway and Ovarian Cancer EtiologyR01CA122443 · NCI · MAYO CLINIC ROCHESTER · PI GOODE, ELLEN L. · 2007 to 2012
$2.7M
Delineating a New Mechanism of Foreign DNA Restriction in Human CellsF32GM095219 · NIGMS · UNIVERSITY OF MINNESOTA · PI CARPENTER, MICHAEL ALLEN · 2010 to 2012
$124k
NCATS NIH HHS UL1 TR000114NCI NIH HHS BC101124NCI NIH HHS NIH P30 CA15083NCI NIH HHS NIH P50 CA136393NCI NIH HHS P30 CA015083NCI NIH HHS P30 CA077598NCI NIH HHS P30 CA77598NCI NIH HHS P50 CA136393NCI NIH HHS R01 CA122443NCI NIH HHS T32 CA009138NCRR NIH HHS 1UL1RR033183NCRR NIH HHS UL1 RR033183NIAID NIH HHS R01 AI064046NIGMS NIH HHS F32 GM095219NIGMS NIH HHS NIH F32 GM095219NIGMS NIH HHS P01 GM091743
6 · The paper itself

Abstract

Ovarian cancer is a clinically and molecularly heterogeneous disease. The driving forces behind this variability are unknown. Here, we report wide variation in the expression of the DNA cytosine deaminase APOBEC3B, with elevated expression in the majority of ovarian cancer cell lines (three SDs above the mean of normal ovarian surface epithelial cells) and high-grade primary ovarian cancers. APOBEC3B is active in the nucleus of several ovarian cancer cell lines and elicits a biochemical preference for deamination of cytosines in 5'-TC dinucleotides. Importantly, examination of whole-genome sequence from 16 ovarian cancers reveals that APOBEC3B expression correlates with total mutation load as well as elevated levels of transversion mutations. In particular, high APOBEC3B expression correlates with C-to-A and C-to-G transversion mutations within 5'-TC dinucleotide motifs in early-stage high-grade serous ovarian cancer genomes, suggesting that APOBEC3B-catalyzed genomic uracil lesions are further processed by downstream DNA "repair" enzymes including error-prone translesion polymerases. These data identify a potential role for APOBEC3B in serous ovarian cancer genomic instability.

Indexed as

MutationCarcinoma, Ovarian EpithelialCell Line, TumorCystadenocarcinoma, SerousCytidine DeaminaseFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Knockdown TechniquesGenomicsHumansMinor Histocompatibility AntigensNeoplasms, Glandular and EpithelialOvarian NeoplasmsRNA, MessengerUp-RegulationAPOBEC3B protein, humanCytidine DeaminaseMinor Histocompatibility AntigensRNA, Messenger

Identifiers

PMID24154874
PMCPMC3867573
OpenAlexW2147098985

What OpenQuestion holds

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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.